3beta-Hydroxyergosta-8,24(28)-dien-7-one

Details

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Internal ID e2d055dd-1e9a-4702-973c-8c525ba6916c
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,5R,10S,13R,14R,17R)-3-hydroxy-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,5,6,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one
SMILES (Canonical) CC(C)C(=C)CCC(C)C1CCC2C1(CCC3=C2C(=O)CC4C3(CCC(C4)O)C)C
SMILES (Isomeric) C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CCC3=C2C(=O)C[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C
InChI InChI=1S/C28H44O2/c1-17(2)18(3)7-8-19(4)22-9-10-23-26-24(12-14-28(22,23)6)27(5)13-11-21(29)15-20(27)16-25(26)30/h17,19-23,29H,3,7-16H2,1-2,4-6H3/t19-,20-,21+,22-,23+,27+,28-/m1/s1
InChI Key XNNFSCUGVQFHNA-KLARHEOWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H44O2
Molecular Weight 412.60 g/mol
Exact Mass 412.334130642 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 7.10
Atomic LogP (AlogP) 6.88
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEBI:70334
CHEMBL1631981
DTXSID101290990
1175710-04-9
3-Hydroxyergosta-8,24(28)-dien-7-one
Q27138675
(3beta,5alpha)-3-hydroxyergosta-8,24(28)-dien-7-one
(3S,5R,10S,13R,14R,17R)-17-[(1R)-1,5-dimethyl-4-methylene-hexyl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one

2D Structure

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2D Structure of 3beta-Hydroxyergosta-8,24(28)-dien-7-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6190 61.90%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7140 71.40%
OATP2B1 inhibitior - 0.7231 72.31%
OATP1B1 inhibitior + 0.8094 80.94%
OATP1B3 inhibitior + 0.8829 88.29%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.8290 82.90%
P-glycoprotein inhibitior - 0.4401 44.01%
P-glycoprotein substrate - 0.5691 56.91%
CYP3A4 substrate + 0.6549 65.49%
CYP2C9 substrate - 0.7411 74.11%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.8549 85.49%
CYP2C9 inhibition - 0.8814 88.14%
CYP2C19 inhibition - 0.6937 69.37%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.9233 92.33%
CYP2C8 inhibition - 0.7450 74.50%
CYP inhibitory promiscuity - 0.7382 73.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5937 59.37%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.9149 91.49%
Skin irritation + 0.6105 61.05%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.7374 73.74%
Human Ether-a-go-go-Related Gene inhibition - 0.6660 66.60%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5181 51.81%
skin sensitisation + 0.4801 48.01%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.4585 45.85%
Acute Oral Toxicity (c) III 0.8344 83.44%
Estrogen receptor binding + 0.7699 76.99%
Androgen receptor binding + 0.7310 73.10%
Thyroid receptor binding + 0.7137 71.37%
Glucocorticoid receptor binding + 0.8828 88.28%
Aromatase binding + 0.6294 62.94%
PPAR gamma + 0.6084 60.84%
Honey bee toxicity - 0.7395 73.95%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9951 99.51%

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 97.85% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.89% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.53% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.48% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.71% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.93% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.00% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 90.41% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.74% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.92% 100.00%
CHEMBL1871 P10275 Androgen Receptor 87.45% 96.43%
CHEMBL1902 P62942 FK506-binding protein 1A 86.58% 97.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.05% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.97% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.66% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.84% 92.62%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.65% 91.24%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.37% 92.88%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.78% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.70% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.40% 93.03%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.40% 93.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 50899856
LOTUS LTS0090687
wikiData Q27138675