NCBI Taxonomy: 5502

Curvularia (ncbi_taxid: 5502)

found 162 associated metabolites at genus taxonomy rank level.

Ancestor: Pleosporaceae

Child Taxonomies: Curvularia lunata, Curvularia pisi, Curvularia soli, Curvularia lolii, Curvularia akaii, Curvularia aeria, Curvularia inaequalis, Curvularia arcana, Curvularia reesii, Curvularia malina, Curvularia oryzae, Curvularia fallax, Curvularia panici, Curvularia tsudae, Curvularia ryleyi, Curvularia coicis, Curvularia indica, Curvularia nodosa, Curvularia brachyspora, Curvularia tribuli, Curvularia platzii, Curvularia falcata, Curvularia spicata, Curvularia robusta, Curvularia kusanoi, Curvularia miyakei, Curvularia ellisii, Curvularia hominis, Curvularia sesuvii, Curvularia harveyi, Curvularia ovoidea, Curvularia affinis, Curvularia clavata, Curvularia moringae, Curvularia rouhanii, Curvularia beasleyi, Curvularia boeremae, Curvularia trifolii, Curvularia crepinii, Curvularia micropus, Curvularia buchloes, Curvularia flexuosa, Curvularia uncinata, Curvularia prasadii, Curvularia ischaemi, Curvularia asiatica, Curvularia bannonii, Curvularia alcornii, Curvularia sorghina, Curvularia aurantia, Curvularia nicotiae, Curvularia nodulosa, Curvularia patereae, Curvularia fraserae, Curvularia gladioli, Curvularia austriaca, Curvularia cactivora, Curvularia colbranii, Curvularia kenpeggii, Curvularia mebaldsii, Curvularia palmicola, Curvularia coicicola, Curvularia coatesiae, Curvularia plantarum, Curvularia polytrata, Curvularia americana, Curvularia australis, Curvularia simmonsii, Curvularia tanzanica, Curvularia crustacea, Curvularia neoindica, Curvularia borreriae, Curvularia micrairae, Curvularia siddiquii, Curvularia verrucosa, Curvularia spicifera, Curvularia penniseti, Curvularia hustoniae, Curvularia perotidis, Curvularia ravenelii, Curvularia millisiae, Curvularia deightonii, Curvularia canadensis, Curvularia petersonii, Curvularia cf. nodosa, Curvularia homomorpha, Curvularia geniculata, Curvularia manamgodae, Curvularia radicicola, Curvularia ovariicola, Curvularia tripogonis, Curvularia phaeospora, Curvularia akaiiensis, Curvularia catenulata, Curvularia ahvazensis, Curvularia portulacae, Curvularia tropicalis, Curvularia lonarensis, Curvularia richardiae, Curvularia pallescens, Curvularia intermedia, Curvularia variabilis, Curvularia gudauskasii, Curvularia pandanicola, Curvularia comoriensis, Curvularia matsushimae, Curvularia determinata, Curvularia falsilunata, Curvularia protuberans, Curvularia protuberata, Curvularia tuberculata, Curvularia graminicola, Curvularia mosaddeghii, Curvularia hawaiiensis, Curvularia papendorfii, Curvularia vidyodayana, Curvularia stenotaphri, Curvularia neergaardii, Curvularia lycopersici, Curvularia frankliniae, Curvularia verruculosa, Curvularia andropogonis, Curvularia thailandicum, Curvularia sichuanensis, Curvularia eragrostidis, Curvularia senegalensis, Curvularia cymbopogonis, Curvularia guangxiensis, Curvularia khuzestanica, Curvularia saccharicola, Curvularia eleusinicola, Curvularia curculiginis, Curvularia pseudolunata, Curvularia angsiewkeeae, unclassified Curvularia, Curvularia templetoniae, Curvularia chonburiensis, Curvularia pseudoclavata, Curvularia pseudoellisii, Curvularia eragrosticola, Curvularia sporobolicola, Curvularia warraberensis, Curvularia pseudorobusta, Curvularia joliotcurieae, Curvularia elliptiformis, Curvularia panici-maximi, Curvularia heteropogonis, Curvularia chlamydospora, Curvularia verruciformis, Curvularia bothriochloae, Curvularia dactyloctenii, Curvularia australiensis, Curvularia chuasooengiae, Curvularia crassiseptata, Curvularia lamingtonensis, Curvularia oryzae-sativae, Curvularia subpapendorfii, Curvularia umbiliciformis, Curvularia muehlenbeckiae, Curvularia coimbatorensis, Curvularia tamilnaduensis, Curvularia chiangmaiensis, Curvularia beerburrumensis, Curvularia eragrostidicola, Curvularia caricae-papayae, Curvularia cf. kusanoi G37, Curvularia cf. kusanoi G22, Curvularia cf. kusanoi G12, Curvularia cf. kusanoi G18, Curvularia cf. kusanoi G24, Curvularia radicifoliigena, Curvularia pseudointermedia, Curvularia heteropogonicola, Curvularia pseudoprotuberata, Curvularia dactylocteniicola, Curvularia pseudobrachyspora, Curvularia xishuangbannaensis, Curvularia shahidchamranensis, Curvularia sacchari-officinarum, Curvularia cf. pseudobrachyspora, Curvularia annellidiconidiophora, Curvularia cf. intermedia CV-2021, Curvularia cf. verruculosa CV-2021, Curvularia aff. inaequalis HM-2012, Curvularia cf. coimbatorensis CV-2021, Curvularia cf. brachyspora UFMGCB 6336, Curvularia cf. eragrostidis UFMGCB 5753

(S)-Abscisic acid

(2Z,4E)-5-[(1S)-1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid

C15H20O4 (264.1362)


(+)-abscisic acid is the naturally occurring (1S)-(+) enantiomer of abscisic acid. It is an important sesquiterpenoid plant hormone which acts as a regulator of plant responses to environmental stresses such as drought and cold. It has a role as a plant hormone and a plant metabolite. It is a conjugate acid of a (+)-abscisate. It is an enantiomer of a (-)-abscisic acid. Abscisic acid is a natural product found in Macaranga triloba, Cuscuta pentagona, and other organisms with data available. Abscission-accelerating plant growth substance isolated from young cotton fruit, leaves of sycamore, birch, and other plants, and from potatoes, lemons, avocados, and other fruits. Constituent of cabbage, potato, lemon etc. (S)-Abscisic acid is found in many foods, some of which are common wheat, peach, garden tomato (variety), and yellow wax bean. (S)-Abscisic acid is found in alcoholic beverages. (S)-Abscisic acid is a constituent of cabbage, potato, lemon etc D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids D006133 - Growth Substances > D010937 - Plant Growth Regulators Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2]. Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2].

   

Tryptophol

3-(2-Hydroxyethyl)-1H-indole

C10H11NO (161.0841)


Tryptophol, also known as indole-3-ethanol, is an indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2. It has a role as a Saccharomyces cerevisiae metabolite, an auxin and a plant metabolite. Tryptophol is a catabolite of tryptophan converted by the gut microbiota. After absorption through the intestinal epithelium, tryptophan catabolites enter the bloodstream and are later excreted in the urine (PMID:30120222). Tryptophol production was negatively associated with interferon-gamma production (IFNγ) which suggests that tryptophol has anti-inflammatory properties (PMID:27814509). Tryptophol has also been identified as the hypnotic agent in trypanosomal sleeping sickness, and because it is formed in vivo after ethanol or disulfiram treatment, it is also associated with the study of alcoholism (PMID:7241135). Indole-3-ethanol is a dietary indole present in cruciferous vegetables that has been shown to influence estradiol metabolism in humans and may provide a new chemopreventive approach to estrogen-dependent diseases. (PMID 2342128) Tryptophol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=526-55-6 (retrieved 2024-06-29) (CAS RN: 526-55-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Tryptophol (Indole-3-ethanol) is an endogenous metabolite. Tryptophol (Indole-3-ethanol) is an endogenous metabolite.

   

Androstenedione

(1S,2R,10R,11S,15S)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-ene-5,14-dione

C19H26O2 (286.1933)


Androst-4-en-3,17-dione, also known as androstenedione or delta(4)-androsten-3,17-dione, belongs to androgens and derivatives class of compounds. Those are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Thus, androst-4-en-3,17-dione is considered to be a steroid lipid molecule. Androst-4-en-3,17-dione is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Androst-4-en-3,17-dione can be found in a number of food items such as naranjilla, purslane, common cabbage, and oval-leaf huckleberry, which makes androst-4-en-3,17-dione a potential biomarker for the consumption of these food products. Androst-4-en-3,17-dione can be found primarily in blood, cerebrospinal fluid (CSF), and urine, as well as throughout most human tissues. In humans, androst-4-en-3,17-dione is involved in a couple of metabolic pathways, which include androgen and estrogen metabolism and androstenedione metabolism. Androst-4-en-3,17-dione is also involved in a couple of metabolic disorders, which include 17-beta hydroxysteroid dehydrogenase III deficiency and aromatase deficiency. Moreover, androst-4-en-3,17-dione is found to be associated with rheumatoid arthritis, thyroid cancer , cushings Syndrome, and schizophrenia. Androst-4-en-3,17-dione is a non-carcinogenic (not listed by IARC) potentially toxic compound. Androstenedione is a delta-4 19-carbon steroid that is produced not only in the testis, but also in the ovary and the adrenal cortex. Depending on the tissue type, androstenedione can serve as a precursor to testosterone as well as estrone and estradiol. It is the common precursor of male and female sex hormones. Some androstenedione is also secreted into the plasma and may be converted in peripheral tissues to testosterone and estrogens. Androstenedione originates either from the conversion of dehydroepiandrosterone or from 17-hydroxyprogesterone. It is further converted to either testosterone or estrone. The production of adrenal androstenedione is governed by ACTH, while the production of gonadal androstenedione is under control by gonadotropins. CONFIDENCE standard compound; INTERNAL_ID 396; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9081; ORIGINAL_PRECURSOR_SCAN_NO 9076 CONFIDENCE standard compound; INTERNAL_ID 396; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9111; ORIGINAL_PRECURSOR_SCAN_NO 9108 CONFIDENCE standard compound; INTERNAL_ID 396; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9069; ORIGINAL_PRECURSOR_SCAN_NO 9064 CONFIDENCE standard compound; INTERNAL_ID 396; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9077; ORIGINAL_PRECURSOR_SCAN_NO 9075 CONFIDENCE standard compound; INTERNAL_ID 396; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9113; ORIGINAL_PRECURSOR_SCAN_NO 9112 C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones CONFIDENCE standard compound; INTERNAL_ID 2803 INTERNAL_ID 2803; CONFIDENCE standard compound CONFIDENCE standard compound; INTERNAL_ID 4165

   

Testosterone

17-Hydroxy-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one

C19H28O2 (288.2089)


Testosterone is the primary male sex hormone and anabolic steroid from the androstane class of steroids. It is the most important androgen in potency and quantity for vertebrates. In humans, testosterone plays a key role in the development of male reproductive tissues such as testes and prostate, as well as promoting secondary sexual characteristics such as increased muscle and bone mass, and the growth of body hair. In addition, testosterone is involved in health and well-being, and the prevention of osteoporosis. Testosterone exerts its action through binding to and activation of the androgen receptor. In mammals, testosterone is metabolized mainly in the liver. Approximately 50\\% of testosterone is metabolized via conjugation into testosterone glucuronide and to a lesser extent testosterone sulfate by glucuronosyltransferases and sulfotransferases. An additional 40\\% of testosterone is metabolized in equal proportions into the 17-ketosteroids androsterone and etiocholanolone via the combined actions of 5alpha- and 5beta-reductases, 3alpha-hydroxysteroid dehydrogenase, and 17beta-HSD. Like other steroid hormones, testosterone is derived from cholesterol. The first step in the biosynthesis of testosterone involves the oxidative cleavage of the side-chain of cholesterol by the cholesterol side-chain cleavage enzyme (P450scc, CYP11A1) to give pregnenolone. In the next step, two additional carbon atoms are removed by the CYP17A1 (17alpha-hydroxylase/17,20-lyase) enzyme to yield a variety of C19 steroids. In addition, the 3beta-hydroxyl group is oxidized by 3beta-hydroxysteroid dehydrogenase to produce androstenedione. In the final and rate limiting step, the C17 keto group androstenedione is reduced by 17beta-hydroxysteroid hydrogenase to yield testosterone. Testosterone is synthesized and released by the Leydig cells in the testes that lie between the tubules and comprise less than 5\\% of the total testicular volume. Testosterone diffuses into the seminiferous tubules where it is essential for maintaining spermatogenesis. Some testosterone binds to an androgen-binding protein (ABP) that is produced by the Sertoli cells and is homologous to the sex-hormone binding globulin that transports testosterone in the general circulation. The ABP carries testosterone in the testicular fluid where it maintains the activity of the accessory sex glands and may also help to retain testosterone within the tubule and bind excess free hormone. Some testosterone is converted to estradiol by Sertoli cell-derived aromatase enzyme. Leydig cell steroidogenesis is controlled primarily by luteinizing hormone with negative feedback of testosterone on the hypothalamic-pituitary axis. The requirement of spermatogenesis for high local concentrations of testosterone means that loss of androgen production is likely to be accompanied by loss of spermatogenesis. Indeed, if testicular androgen production is inhibited by the administration of exogenous androgens then spermatogenesis ceases. This is the basis of using exogenous testosterone as a male contraceptive. The largest amounts of testosterone (>95\\%) are produced by the testes in men, while the adrenal glands account for most of the remainder. Testosterone is also synthesized in far smaller total quantities in women by the adrenal glands, thecal cells of the ovaries, and, during pregnancy, by the placenta. Testosterone levels fall by about 1\\% each year in men. Therefore, with increasing longevity and the aging of the population, the number of older men with testosterone deficiency will increase substantially over the next several decades. Serum testosterone levels decrease progressively in aging men, but the rate and magnitude of decrease vary considerably. Approximately 1\\% of healthy young men have total serum testosterone levels below normal; in contrast, approximately 20\\% of healthy men over age 60 years have serum testosterone levels below normal. (PMID: 17904450, 17875487). G - Genito urinary system and sex hormones > G03 - Sex hormones and modulators of the genital system > G03B - Androgens > G03BA - 3-oxoandrosten (4) derivatives D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D000728 - Androgens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid

   

10-Deacetylbaccatin III

7-epi-10-Deacetylbaccatin III

C29H36O10 (544.2308)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.908 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.907 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.902 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.898 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2261 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. IC50 value: Target: Taxols have exhibit antitumor agents. Several of these taxols can be synthesized from 10- Deacetylbaccatin-III. 10-Deacetylbaccine III is the fifth intermediate of paclitaxel biosynthesis. The biosynthetic pathway consists of approximately 20 enzymatic steps but is not fully elucidated. 10-Deacetylbaccine III is an antineoplastic agent and an anti-cancer intermediate. 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. IC50 value: Target: Taxols have exhibit antitumor agents. Several of these taxols can be synthesized from 10- Deacetylbaccatin-III. 10-Deacetylbaccine III is the fifth intermediate of paclitaxel biosynthesis. The biosynthetic pathway consists of approximately 20 enzymatic steps but is not fully elucidated. 10-Deacetylbaccine III is an antineoplastic agent and an anti-cancer intermediate.

   

4-Hydroxy-3-prenylbenzoate

3-dimethylallyl-4-hydroxybenzoic acid

C12H14O3 (206.0943)


   

brefeldin A

Brefeldin, 7-epi

C16H24O4 (280.1675)


D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents D000890 - Anti-Infective Agents > D000935 - Antifungal Agents D000890 - Anti-Infective Agents > D000998 - Antiviral Agents A metabolite from Penicillium brefeldianum that exhibits a wide range of antibiotic activity. relative retention time with respect to 9-anthracene Carboxylic Acid is 1.042 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.035 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.034 [Raw Data] CB245_Brefeldin-A_pos_50eV_isCID-10eV_rep000008.txt [Raw Data] CB245_Brefeldin-A_pos_40eV_isCID-10eV_rep000008.txt [Raw Data] CB245_Brefeldin-A_pos_30eV_isCID-10eV_rep000008.txt [Raw Data] CB245_Brefeldin-A_pos_20eV_isCID-10eV_rep000008.txt [Raw Data] CB245_Brefeldin-A_pos_10eV_isCID-10eV_rep000008.txt Brefeldin A (BFA) is a lactone antibiotic and a specific inhibitor of protein trafficking. Brefeldin A blocks the transport of secreted and membrane proteins from endoplasmic reticulum to Golgi apparatus[1][2]. Brefeldin A is also an autophagy and mitophagy inhibitor[3]. Brefeldin A is a CRISPR/Cas9 activator[5]. Brefeldin A inhibits HSV-1 and has anti-cancer activity[5]. Brefeldin A (BFA) is a lactone antibiotic and a specific inhibitor of protein trafficking. Brefeldin A blocks the transport of secreted and membrane proteins from endoplasmic reticulum to Golgi apparatus[1][2]. Brefeldin A is also an autophagy and mitophagy inhibitor[3]. Brefeldin A is a CRISPR/Cas9 activator[5]. Brefeldin A inhibits HSV-1 and has anti-cancer activity[5].

   

Abscisic acid

2,4-Pentadienoic acid, 5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-, (Z,E)-(S)-(+)-

C15H20O4 (264.1362)


Abscisic acid is found in american cranberry. Abscisic acid is used to regulate ripening of fruit Abscisic acid (ABA) is an isoprenoid plant hormone, which is synthesized in the plastidal 2-C-methyl-d-erythritol-4-phosphate (MEP) pathway; unlike the structurally related sesquiterpenes, which are formed from the mevalonic acid-derived precursor farnesyl diphosphate (FDP), the C15 backbone of ABA is formed after cleavage of C40 carotenoids in MEP. Zeaxanthin is the first committed ABA precursor; a series of enzyme-catalyzed epoxidations and isomerizations, and final cleavage of the C40 carotenoid by a dioxygenation reaction yields the proximal ABA precursor, xanthoxin, which is then further oxidized to ABA. Abamine has been patented by the Japanese researchers Shigeo Yoshida and Tadao Asami, which are very reluctant to make this substance available in general, neither commercially nor for research purposes. Abscisic acid (ABA), also known as abscisin II and dormin, is a plant hormone. It functions in many plant developmental processes, including bud dormancy 2-trans-abscisic acid is an abscisic acid in which the two acyclic double bonds both have trans-geometry. It is a conjugate acid of a 2-trans-abscisate. 2-cis,4-trans-Abscisic acid is a natural product found in Axinella polypoides, Phaseolus vulgaris, and Vernicia fordii with data available. Abscission-accelerating plant growth substance isolated from young cotton fruit, leaves of sycamore, birch, and other plants, and from potatoes, lemons, avocados, and other fruits. D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids D006133 - Growth Substances > D010937 - Plant Growth Regulators It is used to regulate ripening of fruit Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2]. Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2].

   

Anofinic acid

2,2-Dimethyl-2H-1-benzopyran-6-carboxylic acid

C12H12O3 (204.0786)


Anofinic acid is found in mushrooms. Anofinic acid is a metabolite of Lactarius deliciosus. Metabolite of Lactarius deliciosus. Anofinic acid is found in mushrooms.

   

Batatasin II

1-(2,3-Dihydroxy-4,5-dimethoxyphenyl)-2-phenylethane

C16H18O4 (274.1205)


Batatasin II is found in root vegetables. Batatasin II is a constituent of Dioscorea batatas (Chinese yam). Constituent of Dioscorea batatas (Chinese yam). Batatasin II is found in root vegetables.

   

(1R,7S,13S,15S)-2,15-Dihydroxy-7-methyl-6-oxabicyclo[11.3.0]hexadeca-3,11-dien-5-one

1,13-dihydroxy-6-methyl-1H,4H,6H,7H,8H,9H,11aH,12H,13H,14H,14aH-cyclopenta[f]oxacyclotridecan-4-one

C16H24O4 (280.1675)


   

(-)-Abscisic acid

5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid

C15H20O4 (264.1362)


   

10-Deacetylbaccatin III

4-(acetyloxy)-1,9,12,15-tetrahydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0³,¹⁰.0⁴,⁷]heptadec-13-en-2-yl benzoate

C29H36O10 (544.2308)


   

5Z-7-Oxozeaenol

8,9,16-Trihydroxy-14-methoxy-3-methyl-3,4,9,10-tetrahydro-1H-benzo(c)(1)oxacyclotetradecine-1,7(8H)-dione

C19H22O7 (362.1365)


   

2-cis-abscisate

5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid

C15H19O4 (263.1283)


2-cis-abscisate is practically insoluble (in water) and a weakly acidic compound (based on its pKa). 2-cis-abscisate can be found in a number of food items such as common wheat, lemon thyme, black raspberry, and acorn, which makes 2-cis-abscisate a potential biomarker for the consumption of these food products.

   

10-Deacetylbaccatin

7,11-Methano-5H-cyclodeca(3,4)benz(1,2-b)oxet-5-one, 12b-(acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dodecahydro-4,6,9,11-tetrahydroxy-4a,8,13,13-tetramethyl-, (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-

C29H36O10 (544.2308)


10-deacetylbaccatin III is a tetracyclic diterpenoid and a secondary alpha-hydroxy ketone. It is functionally related to a baccatin III. 10-Deacetylbaccatin III is a natural product found in Corylus avellana, Taxus wallichiana, and other organisms with data available. 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. IC50 value: Target: Taxols have exhibit antitumor agents. Several of these taxols can be synthesized from 10- Deacetylbaccatin-III. 10-Deacetylbaccine III is the fifth intermediate of paclitaxel biosynthesis. The biosynthetic pathway consists of approximately 20 enzymatic steps but is not fully elucidated. 10-Deacetylbaccine III is an antineoplastic agent and an anti-cancer intermediate. 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. IC50 value: Target: Taxols have exhibit antitumor agents. Several of these taxols can be synthesized from 10- Deacetylbaccatin-III. 10-Deacetylbaccine III is the fifth intermediate of paclitaxel biosynthesis. The biosynthetic pathway consists of approximately 20 enzymatic steps but is not fully elucidated. 10-Deacetylbaccine III is an antineoplastic agent and an anti-cancer intermediate.

   

Abscisic_acid

(2Z,4E)-5-[(1S)-1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid

C15H20O4 (264.1362)


(+)-abscisic acid is the naturally occurring (1S)-(+) enantiomer of abscisic acid. It is an important sesquiterpenoid plant hormone which acts as a regulator of plant responses to environmental stresses such as drought and cold. It has a role as a plant hormone and a plant metabolite. It is a conjugate acid of a (+)-abscisate. It is an enantiomer of a (-)-abscisic acid. Abscisic acid is a natural product found in Macaranga triloba, Cuscuta pentagona, and other organisms with data available. Abscission-accelerating plant growth substance isolated from young cotton fruit, leaves of sycamore, birch, and other plants, and from potatoes, lemons, avocados, and other fruits. The naturally occurring (1S)-(+) enantiomer of abscisic acid. It is an important sesquiterpenoid plant hormone which acts as a regulator of plant responses to environmental stresses such as drought and cold. D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids D006133 - Growth Substances > D010937 - Plant Growth Regulators 2-cis-abscisic acid is a member of the class of abscisic acids in which the double bond betweeen positions 2 and 3 has cis- (natural) geometry. It has a role as an abscisic acid receptor agonist. It is a conjugate acid of a 2-cis-abscisate. Dormin is a natural product found in Axinella polypoides, Botrytis cinerea, and Leptosphaeria maculans with data available. Abscission-accelerating plant growth substance isolated from young cotton fruit, leaves of sycamore, birch, and other plants, and from potatoes, lemons, avocados, and other fruits. (±)-Abscisic acid is an orally active plant hormone that is present also in animals. (±)-Abscisic acid (ABA) contributes to the regulation of glycemia in mammals[1]. (±)-Abscisic acid is an orally active plant hormone that is present also in animals. (±)-Abscisic acid (ABA) contributes to the regulation of glycemia in mammals[1]. Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2]. Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2].

   

Curvularin

NCGC00179952-02_C16H20O5_2H-3-Benzoxacyclododecin-2,10(1H)-dione, 4,5,6,7,8,9-hexahydro-11,13-dihydroxy-4-methyl-

C16H20O5 (292.1311)


   

Dehydrocurvularin

11,13-dihydroxy-4-methyl-2,4,5,6,7,10-hexahydro-1H-3-benzoxacyclododecine-2,10-dione

C16H18O5 (290.1154)


D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins

   

Cynodontin

1,4,5,8-Tetrahydroxy-2-methylanthraquinone

C15H10O6 (286.0477)


   

Curvularol

Curvularol

C15H22O4 (266.1518)


An organic heterotricyclic compound that is isolated from the fermentation broth of Curvularia sp. RK97-F166. D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins

   

cochliomycin B

cochliomycin B

C22H28O7 (404.1835)


   

cochliomycin A

cochliomycin A

C22H28O7 (404.1835)


   

5-Methoxy-2-methyl-4H-chromen-4-one

5-Methoxy-2-methyl-4H-chromen-4-one

C11H10O3 (190.063)


   

Anofinic acid

2,2-dimethyl-2H-chromene-6-carboxylic acid

C12H12O3 (204.0786)


   

Spiciferone B

Spiciferone B

C14H16O4 (248.1049)


   
   

Testosterone

17beta-hydroxyandrost-4-en-3-one

C19H28O2 (288.2089)


G - Genito urinary system and sex hormones > G03 - Sex hormones and modulators of the genital system > G03B - Androgens > G03BA - 3-oxoandrosten (4) derivatives D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D000728 - Androgens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone An androstanoid having 17beta-hydroxy and 3-oxo groups, together with unsaturation at C-4-C-5.. C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid Origin: Animal; SubCategory_DNP: The sterols, Androstanes CONFIDENCE standard compound; INTERNAL_ID 2802 CONFIDENCE standard compound; INTERNAL_ID 4160 CONFIDENCE standard compound; INTERNAL_ID 8730 Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong.

   

Androstenedione

4-Androstene-3,17-dione

C19H26O2 (286.1933)


C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones Origin: Animal; SubCategory_DNP: The sterols, Androstanes CONFIDENCE standard compound; INTERNAL_ID 8732 INTERNAL_ID 8732; CONFIDENCE standard compound Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong.

   

Abscisic Acid

(+)-Abscisic acid

C15H20O4 (264.1362)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.880 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.877 Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2]. Abscisic acid ((S)-(+)-Abscisic acid), an orally active phytohormone in fruits and vegetables, is an endogenously produced mammalian hormone. Abscisic acid is a growth inhibitor and can regulate many aspects of plant growth and development. Abscisic acid inhibits proton pump (H+-ATPase) and leads to the plasma membrane depolarization in a Ca2+-dependent manner. Abscisic acid, a LANCL2 natural ligand, is a potent insulin-sensitizing compound and has the potential for pre-diabetes, type 2 diabetes and metabolic syndrome[1][2].

   

Tryptophol

5-21-03-00061 (Beilstein Handbook Reference)

C10H11NO (161.0841)


An indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2. Tryptophol (Indole-3-ethanol) is an endogenous metabolite. Tryptophol (Indole-3-ethanol) is an endogenous metabolite.

   

3-ethyl-6-hydroxy-3H-2-benzofuran-1-one

NCGC00385964-01!3-ethyl-6-hydroxy-3H-2-benzofuran-1-one

C10H10O3 (178.063)


   

ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

NCGC00386069-01!ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

C12H14O5 (238.0841)


   

ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

ethyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

C12H14O5 (238.0841)


   
   

BATATASIN II

1-(2,3-Dihydroxy-4,5-dimethoxyphenyl)-2-phenylethane

C16H18O4 (274.1205)


   

Modiolide A

4R,7S,dihydroxy-2Z,5E-decadien-9R-olide

C10H14O4 (198.0892)


   

4-Hydroxy-3-(3-methylbut-2-en-1-yl)benzoic acid

4-Hydroxy-3-(3-methylbut-2-en-1-yl)benzoic acid

C12H14O3 (206.0943)


   

5Z-7-Oxozeaenol

5Z-7-Oxozeaenol

C19H22O7 (362.1365)


A macrolide that is the 7-oxo derivative of zeaenol (the 5Z stereoisomer). Isolated from Fungi, it exhibits cytotoxic, antibacterial and inhibitory activity against NF-kappaB.

   

Zeaenol

Zeaenol

C19H24O7 (364.1522)


A macrolide that is a 14-memebered macrocycle fused to a 3-methoxyphenol ring. Isolated from Fungi and Cochliobolus lunatus, it exhibits antibacterial and inhibitory activity against NF-kappaB.

   

Teslen

(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

C19H28O2 (288.2089)


G - Genito urinary system and sex hormones > G03 - Sex hormones and modulators of the genital system > G03B - Androgens > G03BA - 3-oxoandrosten (4) derivatives D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D000728 - Androgens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid

   

Methyl 2-ethyl-4-(5-hydroxy-4,5-dimethyl-2-oxooxolan-3-yl)-2-methyl-3-oxobutanoate

Methyl 2-ethyl-4-(5-hydroxy-4,5-dimethyl-2-oxooxolan-3-yl)-2-methyl-3-oxobutanoate

C14H22O6 (286.1416)


   

Paecilomycin F

Paecilomycin F

C19H26O7 (366.1678)


A natural product found in Cochliobolus lunatus.

   

7-Epi-Zeaenol

7-Epi-Zeaenol

C19H24O7 (364.1522)


A macrolide that is a C-7 epimer of zeaenol. Isolated from Fungi, it exhibits inhibitory activity against NF-kappaB.

   

3-ethyl-6-hydroxy-3H-2-benzofuran-1-one

3-ethyl-6-hydroxy-3H-2-benzofuran-1-one

C10H10O3 (178.063)


   

2,2-dimethyl-2H-chromene-6-carboxylic acid

2,2-dimethyl-2H-chromene-6-carboxylic acid

C12H12O3 (204.0786)


   

5E-7-oxozeaenol

5E-7-oxozeaenol

C19H22O7 (362.1365)


A macrolide that is the 7-oxo derivative of zeaenol (the 5E stereoisomer). Isolated from Fungi, it exhibits cytotoxic, antibacterial and inhibitory activity against NF-kappaB.

   

11,13-dihydroxy-4-methyl-2,4,5,6,7,10-hexahydro-1H-3-benzoxacyclododecine-2,10-dione

11,13-dihydroxy-4-methyl-2,4,5,6,7,10-hexahydro-1H-3-benzoxacyclododecine-2,10-dione

C16H18O5 (290.1154)


   

(3r,4r,5s,6s,10z)-4,6-dihydroxy-2,3-dimethoxy-3-methyl-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

(3r,4r,5s,6s,10z)-4,6-dihydroxy-2,3-dimethoxy-3-methyl-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

C15H21NO6 (311.1369)


   

methyl 4-chloro-3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylate

methyl 4-chloro-3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylate

C16H11ClO6 (334.0244)


   

(2r)-5-methoxy-2-methyl-2,3-dihydro-1-benzopyran-4-one

(2r)-5-methoxy-2-methyl-2,3-dihydro-1-benzopyran-4-one

C11H12O3 (192.0786)


   

(5s,6s,10s,14s)-5,18-dihydroxy-20-methoxy-8,8,14-trimethyl-7,9,15-trioxatricyclo[15.4.0.0⁶,¹⁰]henicosa-1(21),2,11,17,19-pentaen-16-one

(5s,6s,10s,14s)-5,18-dihydroxy-20-methoxy-8,8,14-trimethyl-7,9,15-trioxatricyclo[15.4.0.0⁶,¹⁰]henicosa-1(21),2,11,17,19-pentaen-16-one

C22H28O7 (404.1835)


   

5-{2-[3-(1-hydroxyethyl)oxiran-2-yl]-2-methoxyethyl}-5-methoxyfuran-2-one

5-{2-[3-(1-hydroxyethyl)oxiran-2-yl]-2-methoxyethyl}-5-methoxyfuran-2-one

C12H18O6 (258.1103)


   

methyl (2r,4s)-4-{6,14-dihydroxy-13-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-15-yl}-4-ethoxy-2-hydroxybutanoate

methyl (2r,4s)-4-{6,14-dihydroxy-13-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-15-yl}-4-ethoxy-2-hydroxybutanoate

C23H26O10 (462.1526)


   

5-hydroxy-2-[(2r)-2-hydroxypropyl]chromen-4-one

5-hydroxy-2-[(2r)-2-hydroxypropyl]chromen-4-one

C12H12O4 (220.0736)


   

(1s,2s,3r,4s,7r,9s,10s,11s,14s)-4-(acetyloxy)-9,11,14-trihydroxy-10,13,16,16-tetramethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

(1s,2s,3r,4s,7r,9s,10s,11s,14s)-4-(acetyloxy)-9,11,14-trihydroxy-10,13,16,16-tetramethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

C29H34O10 (542.2152)


   

(7s)-7-ethyl-4-methoxy-5h,7h,8h-pyrano[3,2-c]pyran-2-one

(7s)-7-ethyl-4-methoxy-5h,7h,8h-pyrano[3,2-c]pyran-2-one

C11H14O4 (210.0892)


   

7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

C19H24O7 (364.1522)


   

10,18-dihydroxy-20-methoxy-7,7,14-trimethyl-6,8,15-trioxatricyclo[15.4.0.0⁵,⁹]henicosa-1(21),2,11,17,19-pentaen-16-one

10,18-dihydroxy-20-methoxy-7,7,14-trimethyl-6,8,15-trioxatricyclo[15.4.0.0⁵,⁹]henicosa-1(21),2,11,17,19-pentaen-16-one

C22H28O7 (404.1835)


   

4-(5-ethyl-3-methyloxolan-2-yl)-4-hydroxy-n-(1-hydroxy-3-methylpentan-2-yl)pent-2-enimidic acid

4-(5-ethyl-3-methyloxolan-2-yl)-4-hydroxy-n-(1-hydroxy-3-methylpentan-2-yl)pent-2-enimidic acid

C18H33NO4 (327.2409)


   

(1s,2s,3r,4s,7r,9s,10s,14s)-4-(acetyloxy)-9,11,14-trihydroxy-10,13,16,16-tetramethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

(1s,2s,3r,4s,7r,9s,10s,14s)-4-(acetyloxy)-9,11,14-trihydroxy-10,13,16,16-tetramethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

C29H34O10 (542.2152)


   

n-(1-hydroxy-3-methylpentan-2-yl)-3-[2-methyl-3-(4-oxohexan-2-yl)oxiran-2-yl]prop-2-enimidic acid

n-(1-hydroxy-3-methylpentan-2-yl)-3-[2-methyl-3-(4-oxohexan-2-yl)oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

(3s,4s,4'r,6s,7r)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-3,4-dihydro-1h-spiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione

(3s,4s,4'r,6s,7r)-7-ethyl-4'-hydroxy-3,4,7-trimethyl-3,4-dihydro-1h-spiro[2-benzopyran-6,2'-oxolane]-5,5',8-trione

C17H22O6 (322.1416)


   

(5r,6r,10z)-6-hydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,4,7-trione

(5r,6r,10z)-6-hydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,4,7-trione

C14H15NO5 (277.095)


   

(8r)-8-ethyl-2,3,8-trimethylchromene-4,7-dione

(8r)-8-ethyl-2,3,8-trimethylchromene-4,7-dione

C14H16O3 (232.1099)


   

5-methoxy-2-methyl-2,3-dihydro-1-benzopyran-4-one

5-methoxy-2-methyl-2,3-dihydro-1-benzopyran-4-one

C11H12O3 (192.0786)


   

3-ethyl-6,7-dihydroxy-3h-2-benzofuran-1-one

3-ethyl-6,7-dihydroxy-3h-2-benzofuran-1-one

C10H10O4 (194.0579)


   

(2s,3s,4s)-3,4-dihydroxy-2-methyl-7-[(1e)-prop-1-en-1-yl]-2h,3h,4h-pyrano[4,3-b]pyran-5-one

(2s,3s,4s)-3,4-dihydroxy-2-methyl-7-[(1e)-prop-1-en-1-yl]-2h,3h,4h-pyrano[4,3-b]pyran-5-one

C12H14O5 (238.0841)


   

(3s,5z,8r,9r,11z)-8,9,16-trihydroxy-14-methoxy-3-methyl-4,8,9,10-tetrahydro-3h-2-benzoxacyclotetradecine-1,7-dione

(3s,5z,8r,9r,11z)-8,9,16-trihydroxy-14-methoxy-3-methyl-4,8,9,10-tetrahydro-3h-2-benzoxacyclotetradecine-1,7-dione

C19H22O7 (362.1365)


   

8-ethyl-3-(hydroxymethyl)-2,8-dimethylchromene-4,7-dione

8-ethyl-3-(hydroxymethyl)-2,8-dimethylchromene-4,7-dione

C14H16O4 (248.1049)


   

n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

(2e,4e,6e)-7-[(2s,4's,4'ar,5'r,7's)-5,5',7'-trimethyl-3,6'-dioxo-3',4',4'a,5',7',8'-hexahydrospiro[furan-2,2'-naphthalen]-4'-yl]-4,6-dimethylhepta-2,4,6-trienoic acid

(2e,4e,6e)-7-[(2s,4's,4'ar,5'r,7's)-5,5',7'-trimethyl-3,6'-dioxo-3',4',4'a,5',7',8'-hexahydrospiro[furan-2,2'-naphthalen]-4'-yl]-4,6-dimethylhepta-2,4,6-trienoic acid

C25H30O5 (410.2093)


   

3-hydroxy-9-methyl-8,17-dioxatricyclo[12.2.1.0⁵,¹⁶]heptadeca-1,3,5(16)-triene-7,12,15-trione

3-hydroxy-9-methyl-8,17-dioxatricyclo[12.2.1.0⁵,¹⁶]heptadeca-1,3,5(16)-triene-7,12,15-trione

C16H16O6 (304.0947)


   

(2e)-3-chloro-3-{5-hydroxy-3-[(1s)-1-hydroxy-2-methoxy-2-oxoethyl]-7-methyl-4-oxochromen-2-yl}prop-2-enoic acid

(2e)-3-chloro-3-{5-hydroxy-3-[(1s)-1-hydroxy-2-methoxy-2-oxoethyl]-7-methyl-4-oxochromen-2-yl}prop-2-enoic acid

C16H13ClO8 (368.0299)


   

6,14-dihydroxy-13-methoxy-4,12-dimethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaen-10-one

6,14-dihydroxy-13-methoxy-4,12-dimethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaen-10-one

C16H14O6 (302.079)


   

methyl (2r,4s)-4-{6,14-dihydroxy-13-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-15-yl}-2-hydroxy-4-methoxybutanoate

methyl (2r,4s)-4-{6,14-dihydroxy-13-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-15-yl}-2-hydroxy-4-methoxybutanoate

C22H24O10 (448.1369)


   

(2s,3r,4s)-7-methylidene-2-[(1e,3e)-penta-1,3-dien-1-yl]-2h,3h,4h-pyrano[2,3-c]pyrrole-3,4,5-triol

(2s,3r,4s)-7-methylidene-2-[(1e,3e)-penta-1,3-dien-1-yl]-2h,3h,4h-pyrano[2,3-c]pyrrole-3,4,5-triol

C13H15NO4 (249.1001)


   

n-(1-hydroxy-3-methylpentan-2-yl)-3-[3-(4-hydroxyhexan-2-yl)-2-methyloxiran-2-yl]prop-2-enimidic acid

n-(1-hydroxy-3-methylpentan-2-yl)-3-[3-(4-hydroxyhexan-2-yl)-2-methyloxiran-2-yl]prop-2-enimidic acid

C18H33NO4 (327.2409)


   

5,12-dihydroxy-14-methoxy-7,15-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-13-carbaldehyde

5,12-dihydroxy-14-methoxy-7,15-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-13-carbaldehyde

C17H14O7 (330.0739)


   

(2z,4e,6r,9r)-6,9-dihydroxydeca-2,4-dienoic acid

(2z,4e,6r,9r)-6,9-dihydroxydeca-2,4-dienoic acid

C10H16O4 (200.1049)


   

(1r,2s,4r,5r,8r,9s,11r)-2-(hydroxymethyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

(1r,2s,4r,5r,8r,9s,11r)-2-(hydroxymethyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

C20H28O5 (348.1937)


   

(2r,3r,5s)-3-hydroxy-5-[(1e,3e,5e,7e,9e,11e,15e)-17-methyl-13,14-dioxononadeca-1,3,5,7,9,11,15-heptaen-1-yl]oxolane-2-carboxylic acid

(2r,3r,5s)-3-hydroxy-5-[(1e,3e,5e,7e,9e,11e,15e)-17-methyl-13,14-dioxononadeca-1,3,5,7,9,11,15-heptaen-1-yl]oxolane-2-carboxylic acid

C25H30O6 (426.2042)


   

13-bromo-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

13-bromo-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

C19H23BrO7 (442.0627)


   

(4r,8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

(4r,8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

C16H18O5 (290.1154)


   

3,4-dihydroxy-2-methyl-7-(prop-1-en-1-yl)-2h,3h,4h-pyrano[4,3-b]pyran-5-one

3,4-dihydroxy-2-methyl-7-(prop-1-en-1-yl)-2h,3h,4h-pyrano[4,3-b]pyran-5-one

C12H14O5 (238.0841)


   

1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,11'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-9',12'-diol

1',2',5'-trimethyl-8'-oxaspiro[oxirane-2,11'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-9',12'-diol

C15H22O4 (266.1518)


   

12-chloro-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

12-chloro-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

C16H17ClO5 (324.0764)


   

(1ar,7r,7as,7br)-1,1,4,7-tetramethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

(1ar,7r,7as,7br)-1,1,4,7-tetramethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O (218.1671)


   

methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate

C11H12O5 (224.0685)


   

7-ethyl-3,4,7-trimethylisochromene-6,8-dione

7-ethyl-3,4,7-trimethylisochromene-6,8-dione

C14H16O3 (232.1099)


   

(1r,2s,7r,8ar)-7-[(3e)-3-(hydroxyimino)prop-1-en-2-yl]-7-methoxy-1,8a-dimethyl-6-oxo-2,8-dihydro-1h-naphthalen-2-yl (2e,4e,6s)-4,6-dimethylocta-2,4-dienoate

(1r,2s,7r,8ar)-7-[(3e)-3-(hydroxyimino)prop-1-en-2-yl]-7-methoxy-1,8a-dimethyl-6-oxo-2,8-dihydro-1h-naphthalen-2-yl (2e,4e,6s)-4,6-dimethylocta-2,4-dienoate

C26H35NO5 (441.2515)


   

5,8-dihydroxy-n-(1-hydroxy-3-methylpentan-2-yl)-4-methoxy-4,6-dimethyldec-2-enimidic acid

5,8-dihydroxy-n-(1-hydroxy-3-methylpentan-2-yl)-4-methoxy-4,6-dimethyldec-2-enimidic acid

C19H37NO5 (359.2672)


   

(1r,1ar,5r,7r,7as,7br)-5-hydroxy-1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

(1r,1ar,5r,7r,7as,7br)-5-hydroxy-1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O3 (250.1569)


   

(1s,2r,5z,7s,8z,10r)-7-hydroxy-2-methyl-3,11-dioxabicyclo[8.1.0]undeca-5,8-dien-4-one

(1s,2r,5z,7s,8z,10r)-7-hydroxy-2-methyl-3,11-dioxabicyclo[8.1.0]undeca-5,8-dien-4-one

C10H12O4 (196.0736)


   

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

(3z,5r,6z,8s,9r,10r)-5,8,9-trihydroxy-10-methyl-5,8,9,10-tetrahydrooxecin-2-one

(3z,5r,6z,8s,9r,10r)-5,8,9-trihydroxy-10-methyl-5,8,9,10-tetrahydrooxecin-2-one

C10H14O5 (214.0841)


   

3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl 14-hydroxyicosa-4,12-dienoate

3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl 14-hydroxyicosa-4,12-dienoate

C26H46O8 (486.3193)


   

7-hydroxy-1,8a-dimethyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-2,8-dihydro-1h-naphthalen-2-yl 4,6-dimethylocta-2,4-dienoate

7-hydroxy-1,8a-dimethyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-2,8-dihydro-1h-naphthalen-2-yl 4,6-dimethylocta-2,4-dienoate

C25H32O5 (412.225)


   

(4r,5s,6s,10z)-4,6-dihydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

(4r,5s,6s,10z)-4,6-dihydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

C14H17NO5 (279.1107)


   

2-({[6-hydroxy-10-methoxy-2-(8-methoxy-8-oxooctyl)-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

2-({[6-hydroxy-10-methoxy-2-(8-methoxy-8-oxooctyl)-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

C38H56O13 (720.3721)


   

3-ethyl-5,6-dihydroxy-3h-2-benzofuran-1-one

3-ethyl-5,6-dihydroxy-3h-2-benzofuran-1-one

C10H10O4 (194.0579)


   

5-hydroxy-6-(penta-1,3-dien-1-yl)-5,6-dihydropyran-2-one

5-hydroxy-6-(penta-1,3-dien-1-yl)-5,6-dihydropyran-2-one

C10H12O3 (180.0786)


   

(4r,8s)-8,11,13-trihydroxy-4-methyl-4,5,6,7,8,9-hexahydro-1h-3-benzoxacyclododecine-2,10-dione

(4r,8s)-8,11,13-trihydroxy-4-methyl-4,5,6,7,8,9-hexahydro-1h-3-benzoxacyclododecine-2,10-dione

C16H20O6 (308.126)


   

3,4-dihydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-carboxylic acid

3,4-dihydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-carboxylic acid

C12H14O5 (238.0841)


   

(3s)-3-ethyl-5,6-dihydroxy-3h-2-benzofuran-1-one

(3s)-3-ethyl-5,6-dihydroxy-3h-2-benzofuran-1-one

C10H10O4 (194.0579)


   

4-[(2r)-2-hydroxybutanoyl]-3-methoxy-5-methylbenzoic acid

4-[(2r)-2-hydroxybutanoyl]-3-methoxy-5-methylbenzoic acid

C13H16O5 (252.0998)


   

(2'e)-6'-hydroxy-4-methoxy-5-methyl-2'-propylidene-6-oxa-4-azaspiro[bicyclo[3.1.0]hexane-2,1'-cyclohexan]-3'-ene-3,5'-dione

(2'e)-6'-hydroxy-4-methoxy-5-methyl-2'-propylidene-6-oxa-4-azaspiro[bicyclo[3.1.0]hexane-2,1'-cyclohexan]-3'-ene-3,5'-dione

C14H17NO5 (279.1107)


   

(3z,5s,6e,9s,10r)-8-chloro-5,9-dihydroxy-10-methyl-5,8,9,10-tetrahydrooxecin-2-one

(3z,5s,6e,9s,10r)-8-chloro-5,9-dihydroxy-10-methyl-5,8,9,10-tetrahydrooxecin-2-one

C10H13ClO4 (232.0502)


   

2-[(1e)-2-carboxy-1-chloroeth-1-en-1-yl]-5-hydroxy-3-(2-methoxy-2-oxoethyl)-4-oxochromene-7-carboxylic acid

2-[(1e)-2-carboxy-1-chloroeth-1-en-1-yl]-5-hydroxy-3-(2-methoxy-2-oxoethyl)-4-oxochromene-7-carboxylic acid

C16H11ClO9 (382.0092)


   

5-hydroxy-2-(2-hydroxypropyl)chromen-4-one

5-hydroxy-2-(2-hydroxypropyl)chromen-4-one

C12H12O4 (220.0736)


   

(1ar,5s,7r,7as,7br)-5-hydroxy-1,1,4,7-tetramethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

(1ar,5s,7r,7as,7br)-5-hydroxy-1,1,4,7-tetramethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O2 (234.162)


   

7-hydroxy-2-methyl-3,11-dioxabicyclo[8.1.0]undeca-5,8-dien-4-one

7-hydroxy-2-methyl-3,11-dioxabicyclo[8.1.0]undeca-5,8-dien-4-one

C10H12O4 (196.0736)


   

8-ethyl-2,3,8-trimethylchromene-4,7-dione

8-ethyl-2,3,8-trimethylchromene-4,7-dione

C14H16O3 (232.1099)


   

4-hydroxy-3-(3-methylbut-3-en-1-yn-1-yl)benzoic acid

4-hydroxy-3-(3-methylbut-3-en-1-yn-1-yl)benzoic acid

C12H10O3 (202.063)


   

(1r,1ar,7r,7as,7br)-1,4-bis(hydroxymethyl)-1,7-dimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

(1r,1ar,7r,7as,7br)-1,4-bis(hydroxymethyl)-1,7-dimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O3 (250.1569)


   

4,6-dimethyl-7-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-6,8-dihydro-5h-naphthalen-1-yl]hepta-2,4,6-trienoic acid

4,6-dimethyl-7-[3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-6,8-dihydro-5h-naphthalen-1-yl]hepta-2,4,6-trienoic acid

C25H30O4 (394.2144)


   

(4r,5s,10e)-4,6-dihydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

(4r,5s,10e)-4,6-dihydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

C14H17NO5 (279.1107)


   

(4r,8e)-7,11,13-trihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

(4r,8e)-7,11,13-trihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

C16H18O6 (306.1103)


   

(1r,2r,2'z,5r,6's)-6'-hydroxy-4-methoxy-5-methyl-2'-propylidene-6-oxa-4-azaspiro[bicyclo[3.1.0]hexane-2,1'-cyclohexan]-3'-ene-3,5'-dione

(1r,2r,2'z,5r,6's)-6'-hydroxy-4-methoxy-5-methyl-2'-propylidene-6-oxa-4-azaspiro[bicyclo[3.1.0]hexane-2,1'-cyclohexan]-3'-ene-3,5'-dione

C14H17NO5 (279.1107)


   

2-(prop-1-en-2-yl)-1-benzofuran-5-carboxylic acid

2-(prop-1-en-2-yl)-1-benzofuran-5-carboxylic acid

C12H10O3 (202.063)


   

(4r,8e)-6,11,13-trihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

(4r,8e)-6,11,13-trihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

C16H18O6 (306.1103)


   

9-formyl-2-({[6-hydroxy-10-methoxy-2-(8-methoxy-8-oxooctyl)-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1-carboxylic acid

9-formyl-2-({[6-hydroxy-10-methoxy-2-(8-methoxy-8-oxooctyl)-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1-carboxylic acid

C38H56O12 (704.3772)


   

(3s,7r,8s,9s)-13-chloro-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

(3s,7r,8s,9s)-13-chloro-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

C19H23ClO7 (398.1132)


   

(3s,8s,9s,11e)-8,9,16-trihydroxy-14-methoxy-3-methyl-4,5,6,8,9,10-hexahydro-3h-2-benzoxacyclotetradecine-1,7-dione

(3s,8s,9s,11e)-8,9,16-trihydroxy-14-methoxy-3-methyl-4,5,6,8,9,10-hexahydro-3h-2-benzoxacyclotetradecine-1,7-dione

C19H24O7 (364.1522)


   

2-methyl-3,4-dihydro-2h-1-benzopyran-4,5-diol

2-methyl-3,4-dihydro-2h-1-benzopyran-4,5-diol

C10H12O3 (180.0786)


   

(2s,5s)-5-(methoxycarbonyl)-5-methyl-4-oxo-2-[(2r)-3-oxobutan-2-yl]heptanoic acid

(2s,5s)-5-(methoxycarbonyl)-5-methyl-4-oxo-2-[(2r)-3-oxobutan-2-yl]heptanoic acid

C14H22O6 (286.1416)


   

6,9-dihydroxydeca-2,4-dienoic acid

6,9-dihydroxydeca-2,4-dienoic acid

C10H16O4 (200.1049)


   

1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O2 (234.162)


   

13-chloro-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

13-chloro-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

C19H23ClO7 (398.1132)


   

3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (4e,12e)-14-hydroxyicosa-4,12-dienoate

3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (4e,12e)-14-hydroxyicosa-4,12-dienoate

C26H46O8 (486.3193)


   

(2e,4e,6e)-4,6-dimethyl-7-[(6s,8r)-3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-6,8-dihydro-5h-naphthalen-1-yl]hepta-2,4,6-trienoic acid

(2e,4e,6e)-4,6-dimethyl-7-[(6s,8r)-3,6,8-trimethyl-7-oxo-2-(2-oxopropyl)-6,8-dihydro-5h-naphthalen-1-yl]hepta-2,4,6-trienoic acid

C25H30O4 (394.2144)


   

6-hydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,4,7-trione

6-hydroxy-2-methoxy-3-methylidene-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,4,7-trione

C14H15NO5 (277.095)


   

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r)-3-[(2s,4r)-4-hydroxyhexan-2-yl]-2-methyloxiran-2-yl]prop-2-enimidic acid

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r)-3-[(2s,4r)-4-hydroxyhexan-2-yl]-2-methyloxiran-2-yl]prop-2-enimidic acid

C18H33NO4 (327.2409)


   

1,1,4,7-tetramethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

1,1,4,7-tetramethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O (218.1671)


   

(2e)-4-[(2r,3s,5r)-5-ethyl-3-methyloxolan-2-yl]-4-hydroxy-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]pent-2-enimidic acid

(2e)-4-[(2r,3s,5r)-5-ethyl-3-methyloxolan-2-yl]-4-hydroxy-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]pent-2-enimidic acid

C18H33NO4 (327.2409)


   

(4s)-4-[(2r,3s,5r)-5-ethyl-3-methyloxolan-2-yl]-4-hydroxy-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]pent-2-enimidic acid

(4s)-4-[(2r,3s,5r)-5-ethyl-3-methyloxolan-2-yl]-4-hydroxy-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]pent-2-enimidic acid

C18H33NO4 (327.2409)


   

(1r,1ar,7r,7as,7br)-1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

(1r,1ar,7r,7as,7br)-1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O2 (234.162)


   

methyl 2-(2-acetyl-5-hydroxy-3-methoxyphenyl)acetate

methyl 2-(2-acetyl-5-hydroxy-3-methoxyphenyl)acetate

C12H14O5 (238.0841)


   

8-ethyl-2-(hydroxymethyl)-3,8-dimethylchromene-4,7-dione

8-ethyl-2-(hydroxymethyl)-3,8-dimethylchromene-4,7-dione

C14H16O4 (248.1049)


   

2-hydroxy-2,6,6,9-tetramethyl-12-oxatetracyclo[6.4.0.0¹,¹¹.0⁵,⁷]dodecan-3-one

2-hydroxy-2,6,6,9-tetramethyl-12-oxatetracyclo[6.4.0.0¹,¹¹.0⁵,⁷]dodecan-3-one

C15H22O3 (250.1569)


   

(3s)-3-ethyl-6-hydroxy-3h-2-benzofuran-1-one

(3s)-3-ethyl-6-hydroxy-3h-2-benzofuran-1-one

C10H10O3 (178.063)


   

9-formyl-2-({[6-hydroxy-10-methoxy-2-(4-methoxy-4-oxobutyl)-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1-carboxylic acid

9-formyl-2-({[6-hydroxy-10-methoxy-2-(4-methoxy-4-oxobutyl)-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1-carboxylic acid

C34H48O12 (648.3146)


   

(2e,4r,5s,6s,8r)-4,5,8-trihydroxy-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-4,6-dimethyldec-2-enimidic acid

(2e,4r,5s,6s,8r)-4,5,8-trihydroxy-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-4,6-dimethyldec-2-enimidic acid

C18H35NO5 (345.2515)


   

(3r,4r,5s,6s,10z)-3,4,6-trihydroxy-2-methoxy-3-methyl-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

(3r,4r,5s,6s,10z)-3,4,6-trihydroxy-2-methoxy-3-methyl-10-propylidene-2-azaspiro[4.5]dec-8-ene-1,7-dione

C14H19NO6 (297.1212)


   

(2r,4r)-2-methyl-3,4-dihydro-2h-1-benzopyran-4,5-diol

(2r,4r)-2-methyl-3,4-dihydro-2h-1-benzopyran-4,5-diol

C10H12O3 (180.0786)


   

1-{4,13,15-trimethyl-11-oxa-3,14-diazapentacyclo[8.8.0.0²,¹².0³,⁷.0¹⁴,¹⁸]octadeca-4,6,8,15,17-pentaen-10-yl}ethanol

1-{4,13,15-trimethyl-11-oxa-3,14-diazapentacyclo[8.8.0.0²,¹².0³,⁷.0¹⁴,¹⁸]octadeca-4,6,8,15,17-pentaen-10-yl}ethanol

C20H24N2O2 (324.1838)


   

(2s,3r,4s)-3,4-dihydroxy-6-methoxy-7-methylidene-2-[(1e,3e)-penta-1,3-dien-1-yl]-2h,3h,4h-pyrano[2,3-c]pyrrol-5-one

(2s,3r,4s)-3,4-dihydroxy-6-methoxy-7-methylidene-2-[(1e,3e)-penta-1,3-dien-1-yl]-2h,3h,4h-pyrano[2,3-c]pyrrol-5-one

C14H17NO5 (279.1107)


   

1,4-bis(hydroxymethyl)-1,7-dimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

1,4-bis(hydroxymethyl)-1,7-dimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O3 (250.1569)


   

5-hydroxy-1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

5-hydroxy-1-(hydroxymethyl)-1,4,7-trimethyl-1ah,2h,5h,6h,7h,7ah,7bh-cyclopropa[e]azulen-3-one

C15H22O3 (250.1569)


   

(2r,3s,4s)-3,4-dihydroxy-2-methyl-7-[(1e)-prop-1-en-1-yl]-2h,3h,4h-pyrano[4,3-b]pyran-5-one

(2r,3s,4s)-3,4-dihydroxy-2-methyl-7-[(1e)-prop-1-en-1-yl]-2h,3h,4h-pyrano[4,3-b]pyran-5-one

C12H14O5 (238.0841)


   

methyl 2-[5-methoxy-4-(3-oxobutan-2-yl)-4,5-dihydrofuran-3-carbonyl]-2-methylbutanoate

methyl 2-[5-methoxy-4-(3-oxobutan-2-yl)-4,5-dihydrofuran-3-carbonyl]-2-methylbutanoate

C16H24O6 (312.1573)


   

2-(hydroxymethyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

2-(hydroxymethyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

C20H28O5 (348.1937)


   

(1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

(1r,2s,4r,5r,8r,9s,11r)-2-({[(2s,5r,6r,7r,9r,10r)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]decan-7-yl]oxy}methyl)-13-isopropyl-5-methyltetracyclo[7.4.0.0²,¹¹.0⁴,⁸]tridec-12-ene-1,9-dicarboxylic acid

C37H54O13 (706.3564)


   

(7s)-7-ethyl-3,4,7-trimethylisochromene-6,8-dione

(7s)-7-ethyl-3,4,7-trimethylisochromene-6,8-dione

C14H16O3 (232.1099)


   

6-(6-hydroxy-3-methyl-4-oxohexan-3-yl)-2,3-dimethylpyran-4-one

6-(6-hydroxy-3-methyl-4-oxohexan-3-yl)-2,3-dimethylpyran-4-one

C14H20O4 (252.1362)


   

(1r,2s,7r,8ar)-7-hydroxy-1,8a-dimethyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-2,8-dihydro-1h-naphthalen-2-yl (2e,4e,6s)-4,6-dimethylocta-2,4-dienoate

(1r,2s,7r,8ar)-7-hydroxy-1,8a-dimethyl-6-oxo-7-(3-oxoprop-1-en-2-yl)-2,8-dihydro-1h-naphthalen-2-yl (2e,4e,6s)-4,6-dimethylocta-2,4-dienoate

C25H32O5 (412.225)


   

(5as,6s,9as,9bs,11as)-9b-methoxy-6,9a,11a-trimethyl-4h,5h,5ah,6h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-1,7-dione

(5as,6s,9as,9bs,11as)-9b-methoxy-6,9a,11a-trimethyl-4h,5h,5ah,6h,8h,9h,10h,11h-cyclopenta[a]phenanthrene-1,7-dione

C21H28O3 (328.2038)


   

13,15-dibromo-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

13,15-dibromo-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

C19H22Br2O7 (519.9732)


   

(4s,8z)-12-chloro-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

(4s,8z)-12-chloro-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

C16H17ClO5 (324.0764)


   

methyl (2r,4r)-4-{6,14-dihydroxy-13-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-15-yl}-4-ethoxy-2-hydroxybutanoate

methyl (2r,4r)-4-{6,14-dihydroxy-13-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-15-yl}-4-ethoxy-2-hydroxybutanoate

C23H26O10 (462.1526)


   

(3r,4ar,5s)-3-hydroxy-3-(3-hydroxyprop-1-en-2-yl)-4a,5-dimethyl-5,6-dihydro-4h-naphthalen-2-one

(3r,4ar,5s)-3-hydroxy-3-(3-hydroxyprop-1-en-2-yl)-4a,5-dimethyl-5,6-dihydro-4h-naphthalen-2-one

C15H20O3 (248.1412)


   

(3s)-3-ethyl-6,7-dihydroxy-3h-2-benzofuran-1-one

(3s)-3-ethyl-6,7-dihydroxy-3h-2-benzofuran-1-one

C10H10O4 (194.0579)