NCBI Taxonomy: 162425
Aspergillus nidulans (ncbi_taxid: 162425)
found 220 associated metabolites at species taxonomy rank level.
Ancestor: Aspergillus subgen. Nidulantes
Child Taxonomies: Aspergillus nidulans TN02A3, Aspergillus nidulans FGSC A4, Aspergillus nidulans NRRL 8112, Aspergillus nidulans var. dentatus, Aspergillus nidulans var. nidulans, Aspergillus nidulans var. acristatus
Cordycepin
C10H13N5O3 (251.10183480000003)
Cordycepin is a 3-deoxyribonucleoside and a member of adenosines. It has a role as an antimetabolite and a nucleoside antibiotic. Cordycepin has been used in trials studying the treatment of Leukemia. Cordycepin is a natural product found in Aspergillus nidulans, Streptomyces sparsogenes, and other organisms with data available. Cordycepin is a purine nucleoside antimetabolite and antibiotic isolated from the fungus Cordyceps militaris with potential antineoplastic, antioxidant, and anti-inflammatory activities. Cordycepin is an inhibitor of polyadenylation, activates AMP-activated protein kinase (AMPK) and reduces mammalian target of rapamycin (mTOR) signaling, which may result in both the induction of tumor cell apoptosis and a decrease in tumor cell proliferation. mTOR, a serine/threonine kinase belonging to the phosphatidylinositol 3-kinase (PI3K)-related kinase (PIKK) family, plays an important role in the PI3K/AKT/mTOR signaling pathway that regulates cell growth and proliferation, and its expression or activity is frequently dysregulated in human cancers. C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D000890 - Anti-Infective Agents > D000935 - Antifungal Agents D009676 - Noxae > D009153 - Mutagens D000970 - Antineoplastic Agents Cordycepin (3'-Deoxyadenosine) is a nucleoside derivative and inhibits IL-1β-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts (RASFs) in a dose-dependent manner[1]. Cordycepin kills Mycobacterium tuberculosis through hijacking the bacterial adenosine kinase[2]. Cordycepin (3'-Deoxyadenosine) is a nucleoside derivative and inhibits IL-1β-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts (RASFs) in a dose-dependent manner[1]. Cordycepin kills Mycobacterium tuberculosis through hijacking the bacterial adenosine kinase[2]. Cordycepin (3'-Deoxyadenosine) is a nucleoside derivative and inhibits IL-1β-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts (RASFs) in a dose-dependent manner[1]. Cordycepin kills Mycobacterium tuberculosis through hijacking the bacterial adenosine kinase[2].
Ergosterol
Ergosterol is a phytosterol consisting of ergostane having double bonds at the 5,6-, 7,8- and 22,23-positions as well as a 3beta-hydroxy group. It has a role as a fungal metabolite and a Saccharomyces cerevisiae metabolite. It is a 3beta-sterol, an ergostanoid, a 3beta-hydroxy-Delta(5)-steroid and a member of phytosterols. A steroid of interest both because its biosynthesis in FUNGI is a target of ANTIFUNGAL AGENTS, notably AZOLES, and because when it is present in SKIN of animals, ULTRAVIOLET RAYS break a bond to result in ERGOCALCIFEROL. Ergosterol is a natural product found in Gladiolus italicus, Ramaria formosa, and other organisms with data available. ergosterol is a metabolite found in or produced by Saccharomyces cerevisiae. A steroid occurring in FUNGI. Irradiation with ULTRAVIOLET RAYS results in formation of ERGOCALCIFEROL (vitamin D2). See also: Reishi (part of). Ergosterol, also known as provitamin D2, belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, ergosterol is considered to be a sterol lipid molecule. Ergosterol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Ergosterol is the biological precursor to vitamin D2. It is turned into viosterol by ultraviolet light, and is then converted into ergocalciferol, which is a form of vitamin D. Ergosterol is a component of fungal cell membranes, serving the same function that cholesterol serves in animal cells. Ergosterol is not found in mammalian cell membranes. A phytosterol consisting of ergostane having double bonds at the 5,6-, 7,8- and 22,23-positions as well as a 3beta-hydroxy group. Ergosterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=57-87-4 (retrieved 2024-07-12) (CAS RN: 57-87-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects.
Biotin
Biotin (also known as vitamin B7 or vitamin H) is one of the B vitamins.[1][2][3] It is involved in a wide range of metabolic processes, both in humans and in other organisms, primarily related to the utilization of fats, carbohydrates, and amino acids.[4] The name biotin, borrowed from the German Biotin, derives from the Ancient Greek word βίοτος (bíotos; 'life') and the suffix "-in" (a suffix used in chemistry usually to indicate 'forming').[5] Biotin appears as a white, needle-like crystalline solid.[6] Biotin is an organic heterobicyclic compound that consists of 2-oxohexahydro-1H-thieno[3,4-d]imidazole having a valeric acid substituent attached to the tetrahydrothiophene ring. The parent of the class of biotins. It has a role as a prosthetic group, a coenzyme, a nutraceutical, a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite, a mouse metabolite, a cofactor and a fundamental metabolite. It is a member of biotins and a vitamin B7. It is a conjugate acid of a biotinate. A water-soluble, enzyme co-factor present in minute amounts in every living cell. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk. Biotin is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Biotin is a natural product found in Lysinibacillus sphaericus, Aspergillus nidulans, and other organisms with data available. Biotin is hexahydro-2-oxo-1H-thieno(3,4-d)imidazole-4-pentanoic acid. Growth factor present in minute amounts in every living cell. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk. The biotin content of cancerous tissue is higher than that of normal tissue. Biotin is an enzyme co-factor present in minute amounts in every living cell. Biotin is also known as vitamin H or B7 or coenzyme R. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk. Biotin has been recognized as an essential nutrient. Our biotin requirement is fulfilled in part through diet, through endogenous reutilization of biotin and perhaps through capture of biotin generated in the intestinal flora. The utilization of biotin for covalent attachment to carboxylases and its reutilization through the release of carboxylase biotin after proteolytic degradation constitutes the biotin cycle. Biotin deficiency is associated with neurological manifestations, skin rash, hair loss and metabolic disturbances that are thought to relate to the various carboxylase deficiencies (metabolic ketoacidosis with lactic acidosis). It has also been suggested that biotin deficiency is associated with protein malnutrition, and that marginal biotin deficiency in pregnant women may be teratogenic. Biotin acts as a carboxyl carrier in carboxylation reactions. There are four biotin-dependent carboxylases in mammals: those of propionyl-CoA (PCC), 3-methylcrotonyl-CoA (MCC), pyruvate (PC) and acetyl-CoA carboxylases (isoforms ACC-1 and ACC-2). All but ACC-2 are mitochondrial enzymes. The biotin moiety is covalently bound to the epsilon amino group of a Lysine residue in each of these carboxylases in a domain 60-80 amino acids long. The domain is structurally similar among carboxylases from bacteria to mammals. There are four biotin-dependent carboxylases in mammals: those of propionyl-CoA (PCC), 3-methylcrotonyl-CoA (MCC), pyruvate (PC) and acetyl-CoA carboxylases (isoforms ACC-1 and ACC-2). All but ACC-2 are mitochondrial enzymes. The biotin moiety is covalently bound to the epsilon amino group of a Lys residue in each of these carboxylases in a domain 60-80 amino acids long. The domain is structurally similar among carboxylases from bacteria to mammals. Evidence is emerging that biotin participates in processes other than classical carboxylation reactions. Specifically, novel roles for biotin in cell signaling, gene expression, and chromatin structure have been identified in recent years. Human cells accumulate biotin by using both the sodium-dependent multivitamin transporter and monocarboxylate transporter 1. These transporters and other biotin-binding proteins partition biotin to compartments involved in biotin signaling: cytoplasm, mitochondria, and nuclei. The activity of cell signals such as biotinyl-AMP, Sp1 and Sp3, nuclear factor (NF)-kappaB, and receptor tyrosine kinases depends on biotin supply. Consistent with a role for biotin and its catabolites in ... Biotin is an enzyme co-factor present in minute amounts in every living cell. Biotin is also known as coenzyme R and vitamin H or B7. It occurs mainly bound to proteins or polypeptides and is abundant in liver, kidney, pancreas, yeast, and milk. Biotin has been recognized as an essential nutrient. Humans fulfill their biotin requirement through their diet through endogenous reutilization of biotin and perhaps through the capture of biotin generated in the intestinal flora. The utilization of biotin for covalent attachment to carboxylases and its reutilization through the release of carboxylase biotin after proteolytic degradation constitutes the biotin cycle. Biotin deficiency is associated with neurological manifestations, skin rash, hair loss, and metabolic disturbances that are thought to relate to the various carboxylase deficiencies (metabolic ketoacidosis with lactic acidosis). It has also been suggested that biotin deficiency is associated with protein malnutrition, and that marginal biotin deficiency in pregnant women may be teratogenic. Biotin acts as a carboxyl carrier in carboxylation reactions. There are four biotin-dependent carboxylases in mammals: those of propionyl-CoA (PCC), 3-methylcrotonyl-CoA (MCC), pyruvate (PC), and acetyl-CoA carboxylases (isoforms ACC-1 and ACC-2). All but ACC-2 are mitochondrial enzymes. The biotin moiety is covalently bound to the epsilon amino group of a lysine residue in each of these carboxylases in a domain 60-80 amino acids long. The domain is structurally similar among carboxylases from bacteria to mammals. Evidence is emerging that biotin participates in processes other than classical carboxylation reactions. Specifically, novel roles for biotin in cell signalling, gene expression, and chromatin structure have been identified in recent years. Human cells accumulate biotin by using both the sodium-dependent multivitamin transporter and monocarboxylate transporter 1. These transporters and other biotin-binding proteins partition biotin to compartments involved in biotin signalling: cytoplasm, mitochondria, and nuclei. The activity of cell signals such as biotinyl-AMP, Sp1 and Sp3, nuclear factor (NF)-kappaB, and receptor tyrosine kinases depends on biotin supply. Consistent with a role for biotin and its catabolites in modulating these cell signals, greater than 2000 biotin-dependent genes have been identified in various human tissues. Many biotin-dependent gene products play roles in signal transduction and localize to the cell nucleus, consistent with a role for biotin in cell signalling. Posttranscriptional events related to ribosomal activity and protein folding may further contribute to the effects of biotin on gene expression. Finally, research has shown that biotinidase and holocarboxylase synthetase mediate covalent binding of biotin to histones (DNA-binding proteins), affecting chromatin structure; at least seven biotinylation sites have been identified in human histones. Biotinylation of histones appears to play a role in cell proliferation, gene silencing, and the cellular response to DNA repair. Roles for biotin in cell signalling and chromatin structure are consistent with the notion that biotin has a unique significance in cell biology (PMID: 15992684, 16011464). Present in many foods; particularly rich sources include yeast, eggs, liver, certain fish (e.g. mackerel, salmon, sardines), soybeans, cauliflower and cow peas. Dietary supplement. Isolated from various higher plant sources, e.g. sweet corn seedlings and radish leaves An organic heterobicyclic compound that consists of 2-oxohexahydro-1H-thieno[3,4-d]imidazole having a valeric acid substituent attached to the tetrahydrothiophene ring. The parent of the class of biotins. [Raw Data] CB004_Biotin_pos_50eV_CB000006.txt [Raw Data] CB004_Biotin_pos_30eV_CB000006.txt [Raw Data] CB004_Biotin_pos_40eV_CB000006.txt [Raw Data] CB004_Biotin_pos_20eV_CB000006.txt [Raw Data] CB004_Biotin_pos_10eV_CB000006.txt [Raw Data] CB004_Biotin_neg_10eV_000006.txt [Raw Data] CB004_Biotin_neg_20eV_000006.txt Biosynthesis Biotin, synthesized in plants, is essential to plant growth and development.[22] Bacteria also synthesize biotin,[23] and it is thought that bacteria resident in the large intestine may synthesize biotin that is absorbed and utilized by the host organism.[18] Biosynthesis starts from two precursors, alanine and pimeloyl-CoA. These form 7-keto-8-aminopelargonic acid (KAPA). KAPA is transported from plant peroxisomes to mitochondria where it is converted to 7,8-diaminopelargonic acid (DAPA) with the help of the enzyme, BioA. The enzyme dethiobiotin synthetase catalyzes the formation of the ureido ring via a DAPA carbamate activated with ATP, creating dethiobiotin with the help of the enzyme, BioD, which is then converted into biotin which is catalyzed by BioB.[24] The last step is catalyzed by biotin synthase, a radical SAM enzyme. The sulfur is donated by an unusual [2Fe-2S] ferredoxin.[25] Depending on the species of bacteria, Biotin can be synthesized via multiple pathways.[24] Biotin (Vitamin B7) is a water-soluble B vitamin and serves as a coenzyme for five carboxylases in humans, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids[1][2][3]. Biotin, vitamin B7 and serves as a coenzyme for five carboxylases in humans, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids[1][2][3]. Biotin (Vitamin B7) is a water-soluble B vitamin and serves as a coenzyme for five carboxylases in humans, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids[1][2][3].
Amyrin
Beta-amyrin is a pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. It has a role as a plant metabolite and an Aspergillus metabolite. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an oleanane. beta-Amyrin is a natural product found in Ficus pertusa, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Centaurium erythraea whole (part of). A pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].
Indolepyruvate
The thiamin diphosphate (ThDP)-dependent enzyme indolepyruvate decarboxylase (IPDC) is involved in the biosynthetic pathway of the phytohormone 3-indoleacetic acid and catalyzes the nonoxidative decarboxylation of 3-indolepyruvate to 3-indoleacetaldehyde and carbon dioxide. (PMID:15835904)  In addition, the enzyme was compared with the phenylpyruvate decarboxylase from Azospirillum brasilense and the indolepyruvate decarboxylase from Enterobacter cloacae. (PMID:21501384) Indole-3-pyruvate is a microbial metabolite, urinary indole-3-pyruvate is produced by Clostridium sporogenes (PMID:29168502) and Trypanasoma brucei (PMID:27856732). Indolepyruvate, also known as indolepyruvic acid or (indol-3-yl)pyruvate, belongs to indolyl carboxylic acids and derivatives class of compounds. Those are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring. Indolepyruvate is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Indolepyruvate can be found in a number of food items such as spelt, strawberry, gram bean, and oregon yampah, which makes indolepyruvate a potential biomarker for the consumption of these food products. Indolepyruvate exists in all eukaryotes, ranging from yeast to humans. D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants D002491 - Central Nervous System Agents > D000927 - Anticonvulsants D000975 - Antioxidants > D016166 - Free Radical Scavengers D020011 - Protective Agents > D000975 - Antioxidants KEIO_ID I002
N-Acetyltryptophan
N-Acetyl-L-tryptophan or N-Acetyltryptophan, belongs to the class of organic compounds known as N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. N-Acetyltryptophan can also be classified as an alpha amino acid or a derivatized alpha amino acid. Technically, N-Acetyltryptophan is a biologically available N-terminal capped form of the proteinogenic alpha amino acid L-tryptophan. N-acetyl amino acids can be produced either via direct synthesis of specific N-acetyltransferases or via the proteolytic degradation of N-acetylated proteins by specific hydrolases. N-terminal acetylation of proteins is a widespread and highly conserved process in eukaryotes that is involved in protection and stability of proteins (PMID: 16465618). About 85\\\\\% of all human proteins and 68\\\\\% of all yeast proteins are acetylated at their N-terminus (PMID: 21750686). Several proteins from prokaryotes and archaea are also modified by N-terminal acetylation. The majority of eukaryotic N-terminal-acetylation reactions occur through N-acetyltransferase enzymes or NAT’s (PMID: 30054468). These enzymes consist of three main oligomeric complexes NatA, NatB, and NatC, which are composed of at least a unique catalytic subunit and one unique ribosomal anchor. The substrate specificities of different NAT enzymes are mainly determined by the identities of the first two N-terminal residues of the target protein. The human NatA complex co-translationally acetylates N-termini that bear a small amino acid (A, S, T, C, and occasionally V and G) (PMID: 30054468). NatA also exists in a monomeric state and can post-translationally acetylate acidic N-termini residues (D-, E-). NatB and NatC acetylate N-terminal methionine with further specificity determined by the identity of the second amino acid. N-acetylated amino acids, such as N-acetyltryptophan can be released by an N-acylpeptide hydrolase from peptides generated by proteolytic degradation (PMID: 16465618). In addition to the NAT enzymes and protein-based acetylation, N-acetylation of free tryptophan can also occur. Many N-acetylamino acids, including N-acetyltryptophan are classified as uremic toxins if present in high abundance in the serum or plasma (PMID: 26317986; PMID: 20613759). Uremic toxins are a diverse group of endogenously produced molecules that, if not properly cleared or eliminated by the kidneys, can cause kidney damage, cardiovascular disease and neurological deficits (PMID: 18287557). N-Acetyltryptophan has also been used as a protein stabilizer. It prevents protein molecules from oxidative degradation by scavenging oxygen dissolved in protein solutions (PMID: 21903216 ). N-Acetyltryptophan has been identified as a catabolite of tryptophan generated by the gut microbiota. After absorption through the intestinal epithelium, tryptophan catabolites enter the bloodstream and are later excreted in the urine (PMID: 28916042). N-Acetyltryptophan is an inhibitor of cytochrome c release and an antagonist of the neurokinin 1 receptor (NK-1R). These inhibitory effects are thought have a useful role in neuroprotection. For instance, in mouse models of amyotrophic lateral sclerosis (ALS) the administration of N-Acetyltryptophan has been shown delay disease onset, extend survival, and ameliorate deterioration in motor performance ALS transgenic mice (PMID: 25986728). N-acetyltryptophan has been shown to significantly reduce blood-brain barrier permeability and improve functional outcome in rat models of traumatic brain injury (PMID: 29256408). N-Acetyltryptophan has also been shown to have a role in preventing hepatic ischemia-reperfusion injury. This is thought to occur through de-activation of the RIP2/caspase/IL-1beta signaling pathway (PMID: 31184936). D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors Ac-DL-Trp-OH is an endogenous metabolite. Ac-DL-Trp-OH is an endogenous metabolite. N-Acetyl-L-tryptophan is an endogenous metabolite.
Sterigmatocystin
Sterigmatocystin is a mycotoxin of Aspergillus versicolor and Chaetomium species Sterigmatocystin is a poison of the type dermatoxin, from the fungi genus Aspergillus. It appears on crusts of cheese with mold. Sterigmatocystin is a toxic metabolite structurally closely related to the aflatoxins (compare general fact sheet number 2), and consists of a xanthone nucleus attached to a bifuran structure. Sterigmatocystin is mainly produced by the fungi Aspergillus nidulans and A. versicolor. It has been reported in mouldy grain, green coffee beans and cheese although information on its occurrence in foods is limited. It appears to occur much less frequently than the aflatoxins, although analytical methods for its determination have not been as sensitive until recently, and so it is possible that small concentrations in food commodities may not always have been detected. Although it is a potent liver carcinogen similar to aflatoxin B1, current knowledge suggests that it is nowhere near as widespread in its occurrence. If this is the true situation it would be justified to consider sterigmatocystin as no more than a risk to consumers in special or unusual circumstances. Sterigmatocystin is a number of closely related compounds such o-methyl sterigmatocystin are known and some may also occur naturally. The IARC-classification of sterigmatocystin is group 2B, which means it is possibly carcinogenic to humans. In practice, the risk is quite low however, because this substance only appears on cheese crusts with mold, and because of that the chance of daily exposure is very low. Sterigmatocystin is a molded crust is best not to be consumed in whole, but after removing the crust, the cheese can still be consumed. Sterigmatocystin is a different kind of mold than that which appears on cheese itself, which can simply be removed before further consumption D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2320
Cichorine
A member of the class of isoindoles that is 6-hydroxy-4-methoxy-5-methyl-2,3-dihydro-1H-isoindol-1-one which is substituted at position 4, 5, and 6 by methoxy, methyl, and hydroxy groups, respectively. A secondary metabolite found in Aspergillus silvativus, Aspergillus nidulans and Alternaria cichorii, it is poisonous to Russian knapweed (Acroptilon repens).
Norsolorinic acid
A polyketide that is anthraquinone bearing four hydroxy substituents at positions 1, 3, 6 and 8 as well as a hexanoyl substituent at position 2.
Alternariol
Alternariol is found in mushrooms. Alternariol occurs in mycelium of Alternaria tenuis responsible for alternaria cone disorder in hops and fruit spot on papaya (Carica papaya) and Passiflora species.Alternariol is a toxic metabolite of Alternaria fungi. It is an important contaminant in cereals and fruits D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D004791 - Enzyme Inhibitors
O-Demethylfonsecin
O-Demethylfonsecin is a pigment from a mutant of Aspergillus fonsecaeus also known as Aspergillus carbonarius. Pigment from a mutant of Aspergillus fonsecaeus also known as Aspergillus carbonarius.
arugosin A (lactol form)
A dibenzooxepine that is dibenzo[b,e]oxepin-11(6H)-one which is substituted by hydroxy groups at positions 1, 6, and 10, a 3,3-dimethylallyl group at position 2, a 3,3-dimethylallyloxy group at position 7, and a methyl group at position 8.
arugosin B
A dibenzooxepine that is dibenzo[b,e]oxepin-11(6H)-one substituted by hydroxy groups at positions 1, 6 and 10, a methyl group at position 8, a prenyl group at position 4 and a prenyloxy group at position 7. Isolated from Aspergillus, it exhibits antibacterial activity.
Shamixanthone
A pyranoxanthene that is 2,3-dihydropyrano[3,2-a]xanthen-12(1H)-one bearing hydroxy substituents at positions 1 and 11 as well as a prop-1-en-2-yl group at position 2, a methyl substituent at position 5 and a 3,3-dimethylallyl group at position 8. A secondary metabolite produced by Aspergillus nidulans.
β-Amyrin
Beta-amyrin, also known as amyrin or (3beta)-olean-12-en-3-ol, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Thus, beta-amyrin is considered to be an isoprenoid lipid molecule. Beta-amyrin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amyrin can be synthesized from oleanane. Beta-amyrin is also a parent compound for other transformation products, including but not limited to, erythrodiol, glycyrrhetaldehyde, and 24-hydroxy-beta-amyrin. Beta-amyrin can be found in a number of food items such as thistle, pepper (c. baccatum), wakame, and endive, which makes beta-amyrin a potential biomarker for the consumption of these food products. The amyrins are three closely related natural chemical compounds of the triterpene class. They are designated α-amyrin (ursane skeleton), β-amyrin (oleanane skeleton) and δ-amyrin. Each is a pentacyclic triterpenol with the chemical formula C30H50O. They are widely distributed in nature and have been isolated from a variety of plant sources such as epicuticular wax. In plant biosynthesis, α-amyrin is the precursor of ursolic acid and β-amyrin is the precursor of oleanolic acid. All three amyrins occur in the surface wax of tomato fruit. α-Amyrin is found in dandelion coffee . β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].
Emericellin
A xanthone that is xanthen-9-one bearing hydroxymethyl, 3,3-dimethylallyloxy, methyl, 3,3-dimethylallyl and hydroxy groups at positions 1, 2, 3, 5 and 8 respectively. A secondary metabolite produced by Aspergillus nidulans.
asperfuranone
A member of the class of 2-benzofurans that is 6,7-dihydro-2-benzofuran-4(5H)-one that is substituted at positions 5 and 6 by hydroxy groups, at position 5 by a methyl group and at position 1 by a (2E,4E,6S)-4,6-dimethylocta-2,4-dienoyl group (the 5S,6R-diastereoisomer). A polyketide that was first obtained from the fungus Aspergillus nidulans by using a genomic mining approach.
5a-Hydroxy-2-isopropyl-4-(4-oxo-3(4H)-quinazolinyl)-4,5,5a,9c-tetrahydro-3H-2a,9b-diazacyclopenta[jk]fluorene-1,3(2H)-dione
Nidulalin A
A member of the class xanthones which consists of a dihydroxanthone skeleton substituted by hydroxy groups at positions 4 and 8, a methyl group at position 6 and a methoxycarbonyl group at position 4a (the 4R,4aS stereoisomer). It is isolated from Emericella nidulans var lata and Penicillium and exhibits potent antitumour activity against both human and murine tumour cell lines.
3,5-dimethylorsellinic acid
A member of the class of dihydroxybenzoic acids that is o-orsellinic acid carrying two additional methyl substituents at positions 3 and 5.
Secosterigmatocystin
D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
2,4-Dihydroxy-6-methylbenzaldehyde
A dihydroxybenzaldehyde that is 2,4-dihydroxybenzaldehyde in which the hydrogen at position 6 has been replaced by a methyl group. It is a fungal metabolite isolated from Grifola frondosa and Phlebiopsis gigantea.
Sterigmatocystin
An organic heteropentacyclic compound whose skeleton comprises a xanthene ring system ortho-fused to a dihydrofuranofuran moiety. The parent of the class of sterigmatocystins. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins CONFIDENCE Reference Standard (Level 1)
Ergosterol
Indicator of fungal contamination, especies in cereals. Occurs in yeast and fungi. The main fungal steroidand is also found in small amts. in higher plant prods., e.g. palm oil [DFC]. D018977 - Micronutrients > D014815 - Vitamins > D000072664 - Provitamins 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. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects.
Biotin
C10H16N2O3S (244.08815859999999)
A - Alimentary tract and metabolism > A11 - Vitamins D018977 - Micronutrients > D014815 - Vitamins CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2876; ORIGINAL_PRECURSOR_SCAN_NO 2873 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2877; ORIGINAL_PRECURSOR_SCAN_NO 2875 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2896; ORIGINAL_PRECURSOR_SCAN_NO 2894 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2875; ORIGINAL_PRECURSOR_SCAN_NO 2872 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2894; ORIGINAL_PRECURSOR_SCAN_NO 2891 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2908; ORIGINAL_PRECURSOR_SCAN_NO 2906 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6231; ORIGINAL_PRECURSOR_SCAN_NO 6229 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6248; ORIGINAL_PRECURSOR_SCAN_NO 6246 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6251; ORIGINAL_PRECURSOR_SCAN_NO 6246 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6253; ORIGINAL_PRECURSOR_SCAN_NO 6251 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6265; ORIGINAL_PRECURSOR_SCAN_NO 6263 CONFIDENCE standard compound; INTERNAL_ID 1328; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6256; ORIGINAL_PRECURSOR_SCAN_NO 6253 CONFIDENCE standard compound; INTERNAL_ID 219 INTERNAL_ID 219; CONFIDENCE standard compound relative retention time with respect to 9-anthracene Carboxylic Acid is 0.474 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.471 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.469 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.470 Biotin (Vitamin B7) is a water-soluble B vitamin and serves as a coenzyme for five carboxylases in humans, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids[1][2][3]. Biotin, vitamin B7 and serves as a coenzyme for five carboxylases in humans, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids[1][2][3]. Biotin (Vitamin B7) is a water-soluble B vitamin and serves as a coenzyme for five carboxylases in humans, involved in the synthesis of fatty acids, isoleucine, and valine, and in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids[1][2][3].
Alternariol
A benzochromenone that is 6H-benzo[c]chromen-6-one which is substituted by a methyl group at position 1 and by hydroxy groups at positions 3, 7, and 9. It is the most important mycotoxin produced by the black mould Alternaria species, which are the most common mycoflora infecting small grain cereals worldwide. D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors D004791 - Enzyme Inhibitors CONFIDENCE Reference Standard (Level 1)
Indole-3-pyrubate
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants D002491 - Central Nervous System Agents > D000927 - Anticonvulsants D000975 - Antioxidants > D016166 - Free Radical Scavengers D020011 - Protective Agents > D000975 - Antioxidants
Nidulin
N-Acetyl-DL-tryptophan
D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors Ac-DL-Trp-OH is an endogenous metabolite. Ac-DL-Trp-OH is an endogenous metabolite.
(-)-Microperfuranone
A butenolide that is furan-2(5H)-one which is substituted by a phenyl group at position 3, a benzyl group at position 4, and a hydroxy group at position 5 (the (-)-enantiomer). A secondary metabolite obtained from Aspergillus nidulans.
2,4-Dihydroxy-3-methyl-6-(2-oxopropyl)benzaldehyde
A dihydroxybenzaldehyde that is 2,4-dihydroxybenzaldehyde in which the hydrogens at positions 3 and 6 have been replaced by a methyl and 2-oxopropyl groups, respectively.
(2s)-2-{[(2s)-2-{[(2s,3s)-2-{[(2r,3r)-2-{[(2s)-1,3-dihydroxy-2-(6-hydroxy-4-methoxy-5-methyl-1-oxo-3h-isoindol-2-yl)propylidene]amino}-1,3-dihydroxybutylidene]amino}-1-hydroxy-3-methylpentylidene]amino}-1-hydroxyoctylidene]amino}-n-[(2s)-1-hydroxydodecan-2-yl]butanediimidic acid
8-hydroxy-1-(hydroxymethyl)-3-methyl-2-[(3-methylbut-2-en-1-yl)oxy]xanthen-9-one
(8s)-3-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-4h,7h,8h-imidazo[4,5-d][1,3]diazepin-8-ol
6-(5,7-dimethyl-2-oxonona-3,5-dien-1-yl)-2,4-dihydroxy-3-methylbenzaldehyde
6-[2-(5-hydroxy-2,6,6-trimethyloxan-2-yl)ethenyl]-3-methoxy-4-(4-methoxyphenyl)-3h-quinoline-2,4,5-triol
C27H33NO7 (483.22569080000005)
4-(but-2-en-2-yl)-5,13,15-trichloro-6,14-dihydroxy-7,12-dimethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one
(3e)-2-methyl-4-{3-[2-(methylamino)ethyl]-1h-indol-4-yl}but-3-en-2-ol
3,8-dihydroxy-1,10-dimethyl-7h-5-oxa-12-thia-7-azatetraphen-6-one
C17H13NO4S (327.05652580000003)
(2r)-2-[(2s,3r,4r)-3-{6-[(1r,2r,3s,5s)-3-hydroxy-2,3,5-trimethyl-4-oxocyclopentyl]hepta-1,3,5-trien-1-yl}-3,4-dimethyl-5-oxooxolan-2-yl]propanoic acid
(1r,4s,5s,12r,15s,16s)-2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23,24-trithia-3,14-diazahexacyclo[10.9.3.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tetracosa-6,9,17,19-tetraen-5-yl (2r)-2-hydroxy-2-phenylacetate
1-[5-(3,4-dihydroxyphenyl)-2,4-dihydroxypyridin-3-yl]-2,4-dimethylhexan-1-one
C19H23NO5 (345.15761480000003)
(5r,6s,7r,9s,12r,13s)-12-hydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,17,19-triene-11,16-dione
6-methoxy-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindole-1,4-diol
8-hydroxy-2,2',2',9,13-pentamethyl-6,16-dimethylidene-10,14,17-trioxaspiro[pentacyclo[7.6.1.1⁷,¹².0¹,¹².0²,⁷]heptadecane-5,3'-pyran]-6',11,15-trione
3-(3,5-dimethylhepta-1,3-dien-1-yl)-7-methyl-1h-isochromene-1,6,8-triol
(10s)-4,10,15-trihydroxy-13-methyl-7-(3-methylbut-2-en-1-yl)-12-[(3-methylbut-2-en-1-yl)oxy]-9-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-2-one
(1s,2s,5s,9s,10s,11s,12r,13s,14s,16r,17s)-16-[(2s)-1,2-dihydroxypropan-2-yl]-5,9,10,13-tetramethylhexacyclo[9.7.0.0²,⁶.0²,⁹.0¹²,¹⁷.0¹³,¹⁷]octadecane-5,14-diol
2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23-dithia-3,14-diazahexacyclo[10.9.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tricosa-6,9,17,19-tetraen-5-yl 2-hydroxy-2-phenylacetate
(2r)-2-[(2s,3r,4r)-3,4-dimethyl-5-oxo-3-(6,8,10-trimethyl-9-oxododeca-1,3,5,7-tetraen-1-yl)oxolan-2-yl]propanoic acid
6-{2-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]ethenyl}-3-methoxy-4-phenyl-3h-quinoline-2,4,5-triol
6-methoxy-5-{[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3h-isoindole-1,4-diol
7,10,15-trihydroxy-2,4,17-trimethyl-13,20-dioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1(12),4,9,14,16,18-hexaene-6,8,11-trione
2-(1-{1,3-dihydroxy-1-methyl-6-oxo-4h-pyrazino[2,1-b]quinazolin-4-yl}-2-hydroxypropan-2-yl)-5-isopropyl-3-phenylimidazolidin-4-one
4-hydroxy-6,7-dimethyl-8-(2,3,4,5-tetrahydroxypentyl)pteridin-2-one
C13H18N4O6 (326.12262880000003)
5-{[(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}-3h-isoindole-1,4,6-triol
C23H31NO4 (385.22529660000004)
(10s)-4,10,15-trihydroxy-13-methyl-5,7-bis(3-methylbut-2-en-1-yl)-12-[(3-methylbut-2-en-1-yl)oxy]-9-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-2-one
(3r,4r)-3-methoxy-4-(4-methoxyphenyl)-6-[(1e)-2-[(1s,2r,5r)-2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl]ethenyl]-3h-quinoline-2,4,5-triol
1-{4-benzoyl-2-benzyl-5-[(7-methoxy-2h-1,3-benzodioxol-5-yl)methylidene]piperazin-1-yl}ethanone
(2s)-2-{[(2s)-2-{[(3r)-1,3-dihydroxydodecylidene]amino}-1-hydroxy-3-(c-hydroxycarbonimidoyl)propylidene]amino}-n-[(2s)-4-methyl-1-oxopentan-2-yl]pentanediimidic acid
2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23,24,25-tetrathia-3,14-diazahexacyclo[10.9.4.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]pentacosa-6,9,17,19-tetraen-5-yl 2-hydroxy-2-phenylacetate
(1r,12r,14s)-16-hydroxy-14-[(2r,4s)-4-isopropyl-5-oxo-1-phenylimidazolidin-2-yl]-12,14-dimethyl-13-oxa-2,10,17-triazatetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadeca-4,6,8,10,16-pentaen-3-one
C27H29N5O4 (487.22194340000004)
(1s,2r)-1-hydroxy-2,4-dimethyl-1-[(1s,2s,4r,7s,8r,9s)-2,5,7,9-tetramethyl-8-[(1e)-1-[(1s,2s,4r,5r)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]prop-1-en-2-yl]-3-oxatricyclo[5.2.0.0²,⁴]non-5-en-9-yl]pentan-3-one
(2s,4s)-1-[2,4-dihydroxy-5-(4-hydroxyphenyl)pyridin-3-yl]-2,4-dimethylhexan-1-one
C19H23NO4 (329.16269980000004)
4-(but-2-en-2-yl)-5,13,15-trichloro-14-hydroxy-6-methoxy-7,12-dimethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one
(1r,4s,5s,12r,15s,16s)-2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23,24,25-tetrathia-3,14-diazahexacyclo[10.9.4.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]pentacosa-6,9,17,19-tetraen-5-yl (2r)-2-hydroxy-2-phenylacetate
(5r,6s,7r,9r,12s,13s,16s,18r)-12,16,18-trihydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-dien-11-one
(2s)-2-{[(2s)-2-{[(2s,3s)-2-{[(2r,3r)-2-{[(2r)-2-amino-1,3-dihydroxypropylidene]amino}-1,3-dihydroxybutylidene]amino}-1-hydroxy-3-methylpentylidene]amino}-1-hydroxyoctylidene]amino}-n-[(2s)-1-hydroxydodecan-2-yl]butanediimidic acid
(1s,4s,5s,12s,15s,16s)-2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23,24-trithia-3,14-diazahexacyclo[10.9.3.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tetracosa-6,9,17,19-tetraen-5-yl (2r)-2-hydroxy-2-phenylacetate
methyl 3-[(4s,7r)-22-hydroxy-7-(2-hydroxypropan-2-yl)-19-methoxy-10,14-dimethyl-5,23-dioxo-6,17-dioxa-3-azatricyclo[16.3.1.1³,²¹]tricosa-1(22),10,14,18,20-pentaen-4-yl]propanoate
methyl 4,8-dihydroxy-6-methyl-9-oxo-4h-xanthene-4a-carboxylate
(1s,2r)-1-hydroxy-2,4-dimethyl-1-[(1s,2s,3r,4r,5r,6r)-1,3,5,10-tetramethyl-4-[(1e)-1-[(1s,2s,4r,5r)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]prop-1-en-2-yl]-7,8-dioxatricyclo[4.2.2.0²,⁵]dec-9-en-3-yl]pentan-3-one
4-hydroxy-6,7-dimethyl-8-[(2r,3s,4r)-2,3,4,5-tetrahydroxypentyl]pteridin-2-one
C13H18N4O6 (326.12262880000003)
3,8-dihydroxy-1-methoxy-4-[(2s,3s)-1,3,4-trihydroxybutan-2-yl]xanthen-9-one
(2r,5s)-2-{2-hydroxy-1-[(1r,4r)-3-hydroxy-1-methyl-6-oxo-1h,4h-pyrazino[2,1-b]quinazolin-4-yl]propan-2-yl}-5-isopropyl-3-phenylimidazolidin-4-one
(1r,4s,5s,11r,14s,15s)-2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate
C34H28N2O6S2 (624.1388708000001)
1-methyl 5-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl) (2s)-2-{4,6-dihydroxy-1-oxo-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindol-2-yl}pentanedioate
2-(2-hydroxy-1-{3-hydroxy-1-methyl-6-oxo-1h,4h-pyrazino[2,1-b]quinazolin-4-yl}propan-2-yl)-5-isopropyl-3-phenylimidazolidin-4-one
3-methoxy-6-(3-methylbut-2-en-1-yl)-4-phenyl-3h-quinoline-2,4,5-triol
C21H23NO4 (353.16269980000004)
(3s,4s)-4-(4-hydroxyphenyl)-3h-quinoline-2,3,4-triol
2,12-dioxo-15-[(2-phenylacetyl)oxy]-21,22-dithia-3,13-diazahexacyclo[9.9.2.0¹,¹³.0³,¹¹.0⁴,⁹.0¹⁴,¹⁹]docosa-6,8,16,18-tetraen-5-yl 2-phenylacetate
C34H28N2O6S2 (624.1388708000001)
13-[(2s)-4-hydroxy-3,3,5-trimethyl-6-oxo-2h-pyran-2-yl]-3,5,7-trimethyltetradeca-2,4,6,8,10,12-hexaenoic acid
1,5-dimethyl (2s)-2-[4,6-dihydroxy-1-oxo-7-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindol-2-yl]pentanedioate
5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindole-1,4,6-triol
C23H31NO4 (385.22529660000004)
(1s,2s,4as,5r,8ar)-5-(1h-indol-3-ylmethyl)-1,4a-dimethyl-6-methylidene-1-(4-methylpent-3-en-1-yl)-hexahydro-2h-naphthalen-2-ol
(3s,4s)-6-[(1e)-2-[(2r,5r)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]ethenyl]-3-methoxy-4-phenyl-3h-quinoline-2,4,5-triol
3-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-4h,7h,8h-imidazo[4,5-d][1,3]diazepin-8-ol
6-hydroxy-4,7-dimethoxy-5-methyl-3h-2-benzofuran-1-one
1-[(5z)-4-benzoyl-2-benzyl-5-[(7-methoxy-2h-1,3-benzodioxol-5-yl)methylidene]piperazin-1-yl]ethanone
(3s,4s)-3-methoxy-4-phenyl-3h-quinoline-2,4,6-triol
2-[(2s,5s,8r,11s)-5-benzyl-3,6,9,12-tetrahydroxy-8,11-diisopropyl-1,4,7,10-tetraazacyclododeca-1(12),3,6,9-tetraen-2-yl]-1-{2-[(2-methylbut-3-en-2-yl)amino]phenyl}ethanone
5-(1h-indol-3-ylmethyl)-1,4a-dimethyl-6-methylidene-1-(4-methylpent-3-en-1-yl)-hexahydro-2h-naphthalen-2-ol
[5-(6-aminopurin-9-yl)-4-hydroxyoxolan-2-yl]methyl acetate
C12H15N5O4 (293.11239900000004)
(9z,12z)-n-[(3s,6s,9s,11r,15s,18s,20r,21r,24s,25s,26s)-6-[(1s,2s)-1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-5,8,11,17,20,21,23,25-octahydroxy-3,15-bis[(1s)-1-hydroxyethyl]-26-methyl-2,14-dioxo-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0⁹,¹³]heptacosa-4,7,16,22-tetraen-18-yl]octadeca-9,12-dienimidic acid
(1s,2r,5r,7r,8r,9s,12r,13r)-8-hydroxy-2,2',2',9,13-pentamethyl-6,16-dimethylidene-10,14,17-trioxaspiro[pentacyclo[7.6.1.1⁷,¹².0¹,¹².0²,⁷]heptadecane-5,3'-pyran]-6',11,15-trione
(3r,4r)-3-methoxy-4-(4-methoxyphenyl)-6-[(1e)-2-[(1r,2r,5s)-2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl]ethenyl]-3h-quinoline-2,4,5-triol
(9z,12z)-n-[(3s,6s,9s,11r,15s,18s,20r,21r,24s,25s,26s)-6-[(1s,2s)-1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-5,8,11,17,20,21,23,25-octahydroxy-3,15-bis[(1r)-1-hydroxyethyl]-26-methyl-2,14-dioxo-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0⁹,¹³]heptacosa-4,7,16,22-tetraen-18-yl]octadeca-9,12-dienimidic acid
(3s,4s)-3-methoxy-6-(3-methylbut-2-en-1-yl)-4-phenyl-3h-quinoline-2,4,5-triol
C21H23NO4 (353.16269980000004)
methyl (4s,9r)-24-hydroxy-9-(2-hydroxypropan-2-yl)-21-methoxy-12,16-dimethyl-7,25-dioxo-8,19-dioxa-3-azatricyclo[18.3.1.1³,²³]pentacosa-1(24),12,16,20,22-pentaene-4-carboxylate
(2r)-2-[(2s,3r,4r)-3-(9-hydroxy-6,8,10-trimethyldodeca-1,3,5,7,10-pentaen-1-yl)-3,4-dimethyl-5-oxooxolan-2-yl]propanoic acid
3-methoxy-6-{2-[2-methyl-5-(prop-1-en-2-yl)oxolan-2-yl]ethenyl}-4-phenyl-3h-quinoline-2,4,5-triol
C26H29NO5 (435.20456240000004)
3-[3-hydroxy-5-(2-methylpropyl)-1,2-dihydropyrazin-2-yl]propanimidic acid
n-{6-[1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-5,8,11,17,20,21,23,25-octahydroxy-3,15-bis(1-hydroxyethyl)-26-methyl-2,14-dioxo-1,4,7,13,16,22-hexaazatricyclo[22.3.0.0⁹,¹³]heptacosa-4,7,16,22-tetraen-18-yl}octadeca-9,12-dienimidic acid
4-[(2e)-but-2-en-2-yl]-5,13,15-trichloro-6,14-dihydroxy-7,12-dimethyl-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaen-10-one
(5r,6s,7r,12s,13s,18r)-12,18-dihydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-diene-11,16-dione
3-[(2,4-dihydroxy-6-methylphenyl)methyl]-2,4-dihydroxy-6-methylbenzaldehyde
(6s)-6-[(3r,4z)-3-hydroxytridec-4-en-1-yl]oxan-2-one
1-(4,6-dimethylocta-2,4-dienoyl)-5,6-dihydroxy-5-methyl-6,7-dihydro-2-benzofuran-4-one
methyl 24-hydroxy-9-(2-hydroxypropan-2-yl)-21-methoxy-12,16-dimethyl-7,25-dioxo-8,19-dioxa-3-azatricyclo[18.3.1.1³,²³]pentacosa-1(24),12,16,20,22-pentaene-4-carboxylate
5-methyl 1-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl) 2-{4,6-dihydroxy-1-oxo-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindol-2-yl}pentanedioate
10,16,18-trihydroxy-3,5-dioxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹⁴,¹⁹]icosa-1(12),2(9),10,14,16,18-hexaene-13,20-dione
(1s,10s,13r,15s)-1-hydroxy-10-isopropyl-13-(4-oxoquinazolin-3-yl)-8,11-diazatetracyclo[6.6.1.0²,⁷.0¹¹,¹⁵]pentadeca-2,4,6-triene-9,12-dione
(1r,2s,5s,6s,8r,9s,10r,12s,15r,16s,25r,27s,28r)-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-2,5,9,28-tetrol
(1r,2s,5s,6s,8r,9s,10r,12s,15r,16s,25r,27s,28r)-21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-2,5,9,28-tetrol
C37H44ClNO7 (649.2806143999999)
6,8-dihydroxy-3-(2-hydroxy-4-oxopentyl)isochromen-1-one
3-(2,3-dihydroxy-5-methylphenoxy)-4,8-dihydroxy-1,10-dimethyl-7h-5-oxa-12-thia-7-azatetraphen-6-one
C24H19NO7S (465.0882184000001)
n-{7,31-dihydroxy-3,15-bis[(1-hydroxyethylidene)amino]-10,19,22,34-tetramethyl-2,8,14,20,26,32-hexaoxo-1,13,25-trioxa-7,19,31-triazacycloheptatriaconta-9,21,33-trien-27-yl}ethanimidic acid
2-[2,6-dihydroxy-3-(3-methylbut-2-en-1-yl)benzoyl]-3,6-dihydroxy-5-methylbenzaldehyde
(3r,6r)-3,6-dibenzyl-3,6-bis(methylsulfanyl)pyrazine-2,5-diol
(1r,4s,5s,12r,15s,16s)-2,13-dioxo-5-[(2-phenylacetyl)oxy]-8-oxa-22,23-dithia-3,14-diazahexacyclo[10.9.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tricosa-6,9,17,19-tetraen-16-yl 2-phenylacetate
(1s)-1-ethoxy-8-hydroxy-6-methoxy-3,4-dihydro-1h-2-benzopyran-7-carbaldehyde
21-chloro-15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-2,5,9,28-tetrol
C37H44ClNO7 (649.2806143999999)
1-[2,4-dihydroxy-5-(4-hydroxyphenyl)pyridin-3-yl]-2,4-dimethylhexan-1-one
C19H23NO4 (329.16269980000004)
3,4,8-trihydroxy-1,10-dimethyl-7h-5-oxa-12-thia-7-azatetraphen-6-one
(2s)-3-(6-hydroxy-1h-indol-3-yl)-2-[(1-hydroxyethylidene)amino]propanoic acid
methyl 3-[(4s,7r)-19,22-dihydroxy-7-(2-hydroxypropan-2-yl)-10,14-dimethyl-5,23-dioxo-6,17-dioxa-3-azatricyclo[16.3.1.1³,²¹]tricosa-1(22),10,14,18,20-pentaen-4-yl]propanoate
(1r,4s,5s,12r,15s,16s)-16-{[(2r)-2-hydroxy-2-phenylacetyl]oxy}-2,13-dioxo-8,19-dioxa-23,24,25,26-tetrathia-3,14-diazahexacyclo[10.10.4.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²¹]hexacosa-6,9,17,20-tetraen-5-yl (2r)-2-hydroxy-2-phenylacetate
4,6-dihydroxy-12-methyl-9-(3-methylbut-2-en-1-yl)-3-(prop-1-en-2-yl)-3,4-dihydro-2h-1,10-dioxatetraphen-5-one
(2r)-2-[(2s,3r,4r)-3-{6-[(1r,2r,3r,5s)-3-hydroxy-2,3,5-trimethyl-4-oxocyclopentyl]hepta-1,3,5-trien-1-yl}-3,4-dimethyl-5-oxooxolan-2-yl]propanoic acid
methyl 3-[22-hydroxy-7-(2-hydroxypropan-2-yl)-19-methoxy-10,14-dimethyl-5,23-dioxo-6,17-dioxa-3-azatricyclo[16.3.1.1³,²¹]tricosa-1(22),10,14,18,20-pentaen-4-yl]propanoate
(4s,8r)-10,16,18-trihydroxy-3,5-dioxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹⁴,¹⁹]icosa-1(12),2(9),10,14,16,18-hexaene-13,20-dione
12-hydroxy-7-(1-hydroxy-2,3-dimethylbutyl)-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,17,19-triene-11,16-dione
12,16,18-trihydroxy-7-(1-hydroxy-2,3-dimethylbutyl)-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-dien-11-one
(10r)-4,10,15-trihydroxy-13-methyl-5-(3-methylbut-2-en-1-yl)-12-[(3-methylbut-2-en-1-yl)oxy]-9-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaen-2-one
(4as,7s,10as)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2h-phenanthrene
1-methyl 5-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl) 2-{4,6-dihydroxy-1-oxo-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindol-2-yl}pentanedioate
1-ethoxy-8-hydroxy-6-methoxy-3,4-dihydro-1h-2-benzopyran-7-carbaldehyde
(3r,4r)-6-[(1e)-2-(5-hydroxy-2,6,6-trimethyloxan-2-yl)ethenyl]-3-methoxy-4-(4-methoxyphenyl)-3h-quinoline-2,4,5-triol
C27H33NO7 (483.22569080000005)
1-hydroxy-10-isopropyl-13-(4-oxoquinazolin-3-yl)-8,11-diazatetracyclo[6.6.1.0²,⁷.0¹¹,¹⁵]pentadeca-2,4,6-triene-9,12-dione
(5r,6s,7r,9r,12r,13s)-12-hydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,17,19-triene-11,16-dione
2,5-dibenzyl-3-hydroxy-6-methoxypyrazin-1-ium-1-olate
2-methyl-4-{3-[2-(methylamino)ethyl]-1h-indol-4-yl}but-3-en-2-ol
2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23,24-trithia-3,14-diazahexacyclo[10.9.3.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tetracosa-6,9,17,19-tetraen-5-yl 2-hydroxy-2-phenylacetate
(1'r,2's,3r,8's,9's,12'r,13'r)-8',12'-dihydroxy-2,2,2',6',9',13'-hexamethyl-16'-methylidene-10',14'-dioxaspiro[pyran-3,5'-tetracyclo[7.6.1.0¹,¹².0²,⁷]hexadecan]-6'-ene-6,11',15'-trione
methyl 2-(2,6-dihydroxy-4-methylbenzoyl)-6-hydroxybenzoate
(5r,6s,7r,9r,12s,13s,18r)-12,18-dihydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-diene-11,16-dione
(2s)-2-{[(2s)-2-{[(2s,3s)-2-{[(2r,3r)-2-{[(2r)-2-amino-1-hydroxypropylidene]amino}-1,3-dihydroxybutylidene]amino}-1-hydroxy-3-methylpentylidene]amino}-1-hydroxyoctylidene]amino}-n-[(2s)-1-hydroxydodecan-2-yl]butanediimidic acid
(2s,4s)-1-[5-(3,4-dihydroxyphenyl)-2,4-dihydroxypyridin-3-yl]-2,4-dimethylhexan-1-one
C19H23NO5 (345.15761480000003)
16-hydroxy-14-(4-isopropyl-5-oxo-1-phenylimidazolidin-2-yl)-12,14-dimethyl-13-oxa-2,10,17-triazatetracyclo[10.3.2.0²,¹¹.0⁴,⁹]heptadeca-4,6,8,10,16-pentaen-3-one
C27H29N5O4 (487.22194340000004)
(6s)-6-[(3r,4z,7z)-3-hydroxytrideca-4,7-dien-1-yl]oxan-2-one
(1s,2r)-1-hydroxy-2,4-dimethyl-1-[(1r,2r,4s,7r,8s,9r)-2,5,7,9-tetramethyl-8-[(1e)-1-[(1s,2s,4r,5r)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]prop-1-en-2-yl]-3-oxatricyclo[5.2.0.0²,⁴]non-5-en-9-yl]pentan-3-one
(5r,6s,7r,12r,13s)-12-hydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-diene-11,16-dione
3-(2,6-dihydroxy-4-methylphenoxy)-4,8-dihydroxy-1,10-dimethyl-7h-5-oxa-12-thia-7-azatetraphen-6-one
C24H19NO7S (465.0882184000001)
12,18-dihydroxy-7-(1-hydroxy-2,3-dimethylbutyl)-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-diene-11,16-dione
16-[(2-hydroxy-2-phenylacetyl)oxy]-2,13-dioxo-8,19-dioxa-23,24,25,26-tetrathia-3,14-diazahexacyclo[10.10.4.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²¹]hexacosa-6,9,17,20-tetraen-5-yl 2-hydroxy-2-phenylacetate
(3r,7s)-15-hydroxy-11-methoxy-6,8,20-trioxapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,4,9,11,14,16,18-heptaen-13-one
3-(6-hydroxy-1h-indol-3-yl)-2-[(1-hydroxyethylidene)amino]propanoic acid
5-methyl 1-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl) (2s)-2-{4,6-dihydroxy-1-oxo-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindol-2-yl}pentanedioate
1-[(2s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxyoxolan-2-yl]-1-hydroxypropan-2-one
C12H15N5O4 (293.11239900000004)
(1r)-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-7-methyl-1h-isochromene-1,6,8-triol
(3r)-6-hydroxy-3,4-dimethoxy-5-methyl-3h-2-benzofuran-1-one
(1s,2s,5s,8s,9s,10s,11s,12r,13s,14s,16r,17s)-16-(2-hydroxypropan-2-yl)-5,9,10,13-tetramethylhexacyclo[9.7.0.0²,⁶.0²,⁹.0¹²,¹⁷.0¹³,¹⁷]octadecane-5,8,14-triol
1,2,5,6,8-pentahydroxy-3-{[(3,4,5,7,8-pentahydroxy-9,10-dioxoanthracen-2-yl)methoxy]methyl}anthracene-9,10-dione
(2s,3r)-2-[(2r,3s)-3-methyloxiran-2-yl]-6-oxo-2,3-dihydropyran-3-yl acetate
6-[(3e,5e,7s)-5,7-dimethyl-2-oxonona-3,5-dien-1-yl]-2,4-dihydroxy-3-methylbenzaldehyde
(3r,4r)-6-[(1e)-2-[(2s,5r)-5-hydroxy-2,6,6-trimethyloxan-2-yl]ethenyl]-3-methoxy-4-(4-methoxyphenyl)-3h-quinoline-2,4,5-triol
C27H33NO7 (483.22569080000005)
(4s,5s)-2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23,24-trithia-3,14-diazahexacyclo[10.9.3.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tetracosa-6,9,17,19-tetraen-5-yl (2r)-2-hydroxy-2-phenylacetate
1,5-dimethyl 2-[4,6-dihydroxy-1-oxo-7-(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)-5-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)oxy]-3h-isoindol-2-yl]pentanedioate
15,16,33,33-tetramethyl-24-methylidene-10-(prop-1-en-2-yl)-7,11,32-trioxa-18-azadecacyclo[25.4.2.0²,¹⁶.0⁵,¹⁵.0⁶,⁸.0⁶,¹².0¹⁷,³¹.0¹⁹,³⁰.0²²,²⁹.0²⁵,²⁸]tritriaconta-17(31),19,21,29-tetraene-2,5,9,28-tetrol
13-[(2r,3s)-4-hydroxy-3,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-3,5,7-trimethyltetradeca-2,4,6,8,10,12-hexaenoic acid
(2s,4r)-2,4-dimethyl-4-[(1e)-2-[(3s,4s)-2,4,5-trihydroxy-3-methoxy-4-phenyl-3h-quinolin-6-yl]ethenyl]cyclohexan-1-one
C26H29NO5 (435.20456240000004)
8',12'-dihydroxy-2,2,2',6',9',13'-hexamethyl-16'-methylidene-10',14'-dioxaspiro[pyran-3,5'-tetracyclo[7.6.1.0¹,¹².0²,⁷]hexadecan]-6'-ene-6,11',15'-trione
methyl 3-[19,22-dihydroxy-7-(2-hydroxypropan-2-yl)-10,14-dimethyl-5,23-dioxo-6,17-dioxa-3-azatricyclo[16.3.1.1³,²¹]tricosa-1(22),10,14,18,20-pentaen-4-yl]propanoate
[(2s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxyoxolan-2-yl]methyl acetate
C12H15N5O4 (293.11239900000004)
(5r,6s,7r,9s,12s,13s,18r)-12,18-dihydroxy-7-[(1s,2r)-1-hydroxy-2,3-dimethylbutyl]-6,13-dimethylpentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-1,19-diene-11,16-dione
3-methoxy-4-(4-methoxyphenyl)-6-(2-{2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl}ethenyl)-3h-quinoline-2,4,5-triol
(3s,4s)-3-methoxy-6-[(1e)-2-[(2r,5r)-2-methyl-5-(prop-1-en-2-yl)oxolan-2-yl]ethenyl]-4-phenyl-3h-quinoline-2,4,5-triol
C26H29NO5 (435.20456240000004)
(2z,3z)-bis[(4-methoxyphenyl)methylidene]butanedinitrile
C20H16N2O2 (316.12117159999997)
(1r,4s,5s,12r,15s,16s)-2,13-dioxo-16-[(2-phenylacetyl)oxy]-8-oxa-22,23-dithia-3,14-diazahexacyclo[10.9.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0¹⁵,²⁰]tricosa-6,9,17,19-tetraen-5-yl (2r)-2-hydroxy-2-phenylacetate
(2r,5s)-2-{1-[(1s,4r)-1,3-dihydroxy-1-methyl-6-oxo-4h-pyrazino[2,1-b]quinazolin-4-yl]-2-hydroxypropan-2-yl}-5-isopropyl-3-phenylimidazolidin-4-one
6,8-dihydroxy-3-[(2r)-2-hydroxy-4-oxopentyl]isochromen-1-one
2-{[2-({2-[(2-{[1,3-dihydroxy-2-(6-hydroxy-4-methoxy-5-methyl-1-oxo-3h-isoindol-2-yl)propylidene]amino}-1,3-dihydroxybutylidene)amino]-1-hydroxy-3-methylpentylidene}amino)-1-hydroxyoctylidene]amino}-n-(1-hydroxydodecan-2-yl)butanediimidic acid
(6z)-3-benzyl-3-(methylsulfanyl)-6-(phenylmethylidene)pyrazine-2,5-diol
C19H18N2O2S (338.10889280000004)
