Cerevisterol

Details

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Internal ID a7a2139e-542e-468d-8534-b9e7487cf2c0
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,5R,6R,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-1,2,3,4,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol
SMILES (Canonical) CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC(C4(C3(CCC(C4)O)C)O)O)C
SMILES (Isomeric) C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=C[C@H]([C@@]4([C@@]3(CC[C@@H](C4)O)C)O)O)C
InChI InChI=1S/C28H46O3/c1-17(2)18(3)7-8-19(4)22-9-10-23-21-15-25(30)28(31)16-20(29)11-14-27(28,6)24(21)12-13-26(22,23)5/h7-8,15,17-20,22-25,29-31H,9-14,16H2,1-6H3/b8-7+/t18-,19+,20-,22+,23-,24-,25+,26+,27+,28-/m0/s1
InChI Key ARXHRTZAVQOQEU-BRVLHLJYSA-N
Popularity 47 references in papers

Physical and Chemical Properties

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Molecular Formula C28H46O3
Molecular Weight 430.70 g/mol
Exact Mass 430.34469533 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.50
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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516-37-0
Cerevisterin
6MHQ9J8E6J
CHEBI:68083
(3S,5R,6R,9S,10R,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-1,2,3,4,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol
Ergosta-7,22-diene-3,5,6-triol, (3beta,5alpha,6beta,22E)-
C28H46O3
5alpha-Ergosta-7,22-diene-3beta,5,6-triol
Ergosta-7,22-diene-3beta,5alpha,6beta-triol
UNII-6MHQ9J8E6J
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cerevisterol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 - 0.5564 55.64%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6139 61.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7342 73.42%
OATP1B3 inhibitior + 0.9437 94.37%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6689 66.89%
P-glycoprotein inhibitior - 0.6696 66.96%
P-glycoprotein substrate - 0.5972 59.72%
CYP3A4 substrate + 0.6519 65.19%
CYP2C9 substrate - 0.7713 77.13%
CYP2D6 substrate - 0.7725 77.25%
CYP3A4 inhibition - 0.9227 92.27%
CYP2C9 inhibition - 0.8201 82.01%
CYP2C19 inhibition - 0.7174 71.74%
CYP2D6 inhibition - 0.9415 94.15%
CYP1A2 inhibition - 0.8633 86.33%
CYP2C8 inhibition - 0.7387 73.87%
CYP inhibitory promiscuity - 0.8432 84.32%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5569 55.69%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9666 96.66%
Skin irritation + 0.5538 55.38%
Skin corrosion - 0.9311 93.11%
Ames mutagenesis - 0.6970 69.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4454 44.54%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5542 55.42%
skin sensitisation - 0.7004 70.04%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.8400 84.00%
Acute Oral Toxicity (c) I 0.5626 56.26%
Estrogen receptor binding + 0.8586 85.86%
Androgen receptor binding + 0.6522 65.22%
Thyroid receptor binding + 0.6967 69.67%
Glucocorticoid receptor binding + 0.7340 73.40%
Aromatase binding - 0.5111 51.11%
PPAR gamma - 0.5203 52.03%
Honey bee toxicity - 0.8109 81.09%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9836 98.36%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 98.36% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 96.09% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.65% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.29% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.45% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.99% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.55% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.51% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.99% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.02% 97.14%
CHEMBL226 P30542 Adenosine A1 receptor 85.03% 95.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.07% 93.56%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 83.70% 95.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.32% 94.75%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.65% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.48% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.21% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Acorus calamus
Azadirachta indica
Bupleurum falcatum
Cynodon dactylon
Macaranga conifera
Melia azedarach

Cross-Links

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PubChem 10181133
NPASS NPC204188
LOTUS LTS0263436
wikiData Q15410887