NCBI Taxonomy: 5503

Curvularia lunata (ncbi_taxid: 5503)

found 89 associated metabolites at species taxonomy rank level.

Ancestor: Curvularia

Child Taxonomies: Curvularia lunata CX-3, Curvularia lunata m118, Curvularia lunata var. lunata

(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].

   

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.

   

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].

   

(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].

   

Cynodontin

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

C15H10O6 (286.0477)


   

cochliomycin B

cochliomycin B

C22H28O7 (404.1835)


   

cochliomycin A

cochliomycin A

C22H28O7 (404.1835)


   
   

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].

   

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)


   

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

   

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)


   

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.

   

(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)


   

(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)


   

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)


   

(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)


   

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)


   

(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)


   

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)


   

(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)


   

(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)


   

(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)


   

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)


   

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

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

C10H10O4 (194.0579)


   

(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)


   

(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)


   

(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)


   

(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)


   

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)


   

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)


   

(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)


   

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)


   

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)


   

(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)


   

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)


   

(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)


   

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

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

C15H22O2 (234.162)


   

(1r,6s,11as,13r,14ar)-1,13-dihydroxy-6-methyl-1h,6h,7h,8h,9h,11ah,12h,13h,14h,14ah-cyclopenta[f]oxacyclotridecan-4-one

(1r,6s,11as,13r,14ar)-1,13-dihydroxy-6-methyl-1h,6h,7h,8h,9h,11ah,12h,13h,14h,14ah-cyclopenta[f]oxacyclotridecan-4-one

C16H24O4 (280.1675)


   

(1r,2s,13r,14s,15r,16r,17s,28s)-8,12,14,23,27,28-hexahydroxy-6,21-dimethoxyoctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaene-3,10,18,25-tetrone

(1r,2s,13r,14s,15r,16r,17s,28s)-8,12,14,23,27,28-hexahydroxy-6,21-dimethoxyoctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaene-3,10,18,25-tetrone

C30H22O12 (574.1111)


   

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

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

C15H22O2 (234.162)


   

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

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

C26H35NO5 (441.2515)


   

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

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

C19H22O7 (362.1365)


   

(2e)-3-[(7r,8r)-8-{[(2s,4s)-2,4-dimethylhexanoyl]oxy}-7-hydroxy-7-methyl-6-oxo-8h-isochromen-3-yl]prop-2-enoic acid

(2e)-3-[(7r,8r)-8-{[(2s,4s)-2,4-dimethylhexanoyl]oxy}-7-hydroxy-7-methyl-6-oxo-8h-isochromen-3-yl]prop-2-enoic acid

C21H26O7 (390.1678)


   

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

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

C19H24O7 (364.1522)


   

(2e)-3-[(7r)-7-{[(2s,4s)-2,4-dimethylhexanoyl]oxy}-7-methyl-6,8-dioxoisochromen-3-yl]prop-2-enoic acid

(2e)-3-[(7r)-7-{[(2s,4s)-2,4-dimethylhexanoyl]oxy}-7-methyl-6,8-dioxoisochromen-3-yl]prop-2-enoic acid

C21H24O7 (388.1522)


   

4-deacylwallifoliol

4-deacylwallifoliol

C27H32O9 (500.2046)


   

1,4,5,8-tetrahydroxy-2-methylanthracene-9,10-dione

1,4,5,8-tetrahydroxy-2-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

(3s,5e,7r,8s,9s,11e)-13-chloro-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

(3s,5e,7r,8s,9s,11e)-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-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

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)


   

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

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

C15H22O2 (234.162)


   

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

(1ar,5r,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)


   

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

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

C25H30O6 (426.2042)


   

(2e,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

(2e,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)


   

5,18-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

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)


   

(1s,2s,5r,7r,8s,9r,11r)-2-hydroxy-2,6,6,9-tetramethyl-12-oxatetracyclo[6.4.0.0¹,¹¹.0⁵,⁷]dodecan-3-one

(1s,2s,5r,7r,8s,9r,11r)-2-hydroxy-2,6,6,9-tetramethyl-12-oxatetracyclo[6.4.0.0¹,¹¹.0⁵,⁷]dodecan-3-one

C15H22O3 (250.1569)


   

methyl 5-(hydroxymethyl)furan-2-carboxylate

methyl 5-(hydroxymethyl)furan-2-carboxylate

C7H8O4 (156.0423)


   

(1s,2s,3r,4s,7r,9r,10s,15s)-4-(acetyloxy)-1,9,15-trihydroxy-10,14,17,17-tetramethyl-11,12-dioxo-6-oxatetracyclo[11.3.1.0³,¹⁰.0⁴,⁷]heptadec-13-en-2-yl benzoate

(1s,2s,3r,4s,7r,9r,10s,15s)-4-(acetyloxy)-1,9,15-trihydroxy-10,14,17,17-tetramethyl-11,12-dioxo-6-oxatetracyclo[11.3.1.0³,¹⁰.0⁴,⁷]heptadec-13-en-2-yl benzoate

C29H34O10 (542.2152)


   

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

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

C15H20O3 (248.1412)


   

(5s,9r,10s,14s)-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

(5s,9r,10s,14s)-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)