(20S)-Ergosta-5,24(28)-diene-3beta,4beta,20-triol

Details

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Internal ID d4cd0894-be53-4854-a2e4-67a8c99a8c99
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,4R,8S,9S,10R,13S,14S,17S)-17-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,4-diol
SMILES (Canonical) CC(C)C(=C)CCC(C)(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4O)O)C)C)O
SMILES (Isomeric) CC(C)C(=C)CC[C@@](C)([C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H]([C@@H]4O)O)C)C)O
InChI InChI=1S/C28H46O3/c1-17(2)18(3)11-16-28(6,31)24-10-9-20-19-7-8-22-25(30)23(29)13-15-26(22,4)21(19)12-14-27(20,24)5/h8,17,19-21,23-25,29-31H,3,7,9-16H2,1-2,4-6H3/t19-,20-,21-,23-,24-,25+,26+,27-,28-/m0/s1
InChI Key BHAJTNJZYVSPOE-AHYPRABSSA-N
Popularity 0 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 5.90
Atomic LogP (AlogP) 5.64
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (20S)-Ergosta-5,24(28)-diene-3beta,4beta,20-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 - 0.6260 62.60%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6632 66.32%
OATP2B1 inhibitior - 0.7186 71.86%
OATP1B1 inhibitior + 0.9045 90.45%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6385 63.85%
P-glycoprotein inhibitior - 0.6379 63.79%
P-glycoprotein substrate - 0.6072 60.72%
CYP3A4 substrate + 0.6856 68.56%
CYP2C9 substrate - 0.5858 58.58%
CYP2D6 substrate - 0.7545 75.45%
CYP3A4 inhibition - 0.8327 83.27%
CYP2C9 inhibition - 0.8725 87.25%
CYP2C19 inhibition - 0.7286 72.86%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition - 0.9265 92.65%
CYP2C8 inhibition + 0.4858 48.58%
CYP inhibitory promiscuity - 0.7758 77.58%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6802 68.02%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9463 94.63%
Skin irritation + 0.5383 53.83%
Skin corrosion - 0.9378 93.78%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6993 69.93%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5196 51.96%
skin sensitisation - 0.6444 64.44%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.9390 93.90%
Acute Oral Toxicity (c) III 0.4754 47.54%
Estrogen receptor binding + 0.8281 82.81%
Androgen receptor binding + 0.7013 70.13%
Thyroid receptor binding + 0.6531 65.31%
Glucocorticoid receptor binding + 0.8247 82.47%
Aromatase binding + 0.5856 58.56%
PPAR gamma + 0.5997 59.97%
Honey bee toxicity - 0.7588 75.88%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9947 99.47%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.59% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.67% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.58% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.56% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.53% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.52% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.39% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.26% 96.77%
CHEMBL1871 P10275 Androgen Receptor 89.87% 96.43%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.70% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.66% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 86.45% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.06% 95.89%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.78% 89.62%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.46% 89.05%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.16% 93.56%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.98% 96.61%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 81.72% 95.00%
CHEMBL3820 P35557 Hexokinase type IV 81.27% 91.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.92% 92.62%
CHEMBL226 P30542 Adenosine A1 receptor 80.79% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.67% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.58% 82.69%

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.
Baccharis minutiflora
Cistus halimifolius
Dysoxylum malabaricum
Heliotropium olgae
Sideritis ibanyezii
Tragopogon orientalis

Cross-Links

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PubChem 102446683
NPASS NPC177919
LOTUS LTS0115752
wikiData Q104935839