Ergosta-24(28)-ene-3beta,5alpha,6beta-triol

Details

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Internal ID 0ca45997-0ae9-49e6-8a4b-3a3a927e0d45
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,5R,6R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol
SMILES (Canonical) CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C
SMILES (Isomeric) C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C[C@H]([C@@]4([C@@]3(CC[C@@H](C4)O)C)O)O)C
InChI InChI=1S/C28H48O3/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/h17,19-25,29-31H,3,7-16H2,1-2,4-6H3/t19-,20+,21+,22-,23+,24+,25-,26-,27-,28+/m1/s1
InChI Key ZGVRWNYCQXZLTR-VJENCBHGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H48O3
Molecular Weight 432.70 g/mol
Exact Mass 432.36034539 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 7.00
Atomic LogP (AlogP) 5.72
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 Ergosta-24(28)-ene-3beta,5alpha,6beta-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 - 0.6842 68.42%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4689 46.89%
OATP2B1 inhibitior - 0.5774 57.74%
OATP1B1 inhibitior + 0.8329 83.29%
OATP1B3 inhibitior + 0.8948 89.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7578 75.78%
P-glycoprotein inhibitior - 0.6101 61.01%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.7345 73.45%
CYP2C9 substrate - 0.5858 58.58%
CYP2D6 substrate - 0.7545 75.45%
CYP3A4 inhibition - 0.8663 86.63%
CYP2C9 inhibition - 0.8072 80.72%
CYP2C19 inhibition - 0.6786 67.86%
CYP2D6 inhibition - 0.9444 94.44%
CYP1A2 inhibition - 0.8945 89.45%
CYP2C8 inhibition - 0.5683 56.83%
CYP inhibitory promiscuity - 0.7974 79.74%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6620 66.20%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9263 92.63%
Skin irritation + 0.5276 52.76%
Skin corrosion - 0.9298 92.98%
Ames mutagenesis - 0.5537 55.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6537 65.37%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5498 54.98%
skin sensitisation - 0.6848 68.48%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.8290 82.90%
Acute Oral Toxicity (c) I 0.7568 75.68%
Estrogen receptor binding + 0.7109 71.09%
Androgen receptor binding + 0.8012 80.12%
Thyroid receptor binding + 0.6239 62.39%
Glucocorticoid receptor binding + 0.7483 74.83%
Aromatase binding + 0.6307 63.07%
PPAR gamma + 0.5492 54.92%
Honey bee toxicity - 0.6404 64.04%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9915 99.15%

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 99.03% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.93% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.99% 96.61%
CHEMBL221 P23219 Cyclooxygenase-1 93.85% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.61% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.86% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.53% 82.69%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 91.86% 89.05%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.46% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.31% 100.00%
CHEMBL1871 P10275 Androgen Receptor 90.50% 96.43%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.67% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 89.18% 95.93%
CHEMBL2094135 Q96BI3 Gamma-secretase 87.94% 98.05%
CHEMBL3837 P07711 Cathepsin L 87.47% 96.61%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 86.55% 95.58%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.21% 85.31%
CHEMBL237 P41145 Kappa opioid receptor 84.60% 98.10%
CHEMBL240 Q12809 HERG 84.49% 89.76%
CHEMBL299 P17252 Protein kinase C alpha 84.47% 98.03%
CHEMBL332 P03956 Matrix metalloproteinase-1 84.36% 94.50%
CHEMBL238 Q01959 Dopamine transporter 84.23% 95.88%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 83.55% 99.00%
CHEMBL2996 Q05655 Protein kinase C delta 83.52% 97.79%
CHEMBL2581 P07339 Cathepsin D 82.97% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.93% 92.62%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.32% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.24% 96.47%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.07% 95.50%
CHEMBL4302 P08183 P-glycoprotein 1 81.88% 92.98%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.74% 94.78%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.17% 98.33%
CHEMBL206 P03372 Estrogen receptor alpha 80.36% 97.64%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.32% 97.14%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 80.27% 95.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.16% 90.71%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.03% 93.04%

Cross-Links

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PubChem 14679361
NPASS NPC31618
LOTUS LTS0111396
wikiData Q105375460