5beta,6beta-Epoxyergosta-24(28)-ene-3beta,7beta-diol

Details

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Internal ID e8ef2510-4cd2-4d1a-8501-ae6a7f8093d0
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids
IUPAC Name (1S,2R,5S,7S,9R,10R,11S,12S,15R,16R)-2,16-dimethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecane-5,10-diol
SMILES (Canonical) CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C4C5(C3(CCC(C5)O)C)O4)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]2[C@H]([C@@H]4[C@]5([C@@]3(CC[C@@H](C5)O)C)O4)O)C
InChI InChI=1S/C28H46O3/c1-16(2)17(3)7-8-18(4)20-9-10-21-23-22(12-13-26(20,21)5)27(6)14-11-19(29)15-28(27)25(31-28)24(23)30/h16,18-25,29-30H,3,7-15H2,1-2,4-6H3/t18-,19+,20-,21+,22+,23+,24-,25-,26-,27-,28-/m1/s1
InChI Key XHDGWDKXAGPPLU-BVHIWFKGSA-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) 53.00 Ų
XlogP 7.10
Atomic LogP (AlogP) 5.74
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5beta,6beta-Epoxyergosta-24(28)-ene-3beta,7beta-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 - 0.6015 60.15%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4548 45.48%
OATP2B1 inhibitior - 0.5763 57.63%
OATP1B1 inhibitior + 0.8572 85.72%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6920 69.20%
P-glycoprotein inhibitior - 0.5982 59.82%
P-glycoprotein substrate - 0.6030 60.30%
CYP3A4 substrate + 0.7381 73.81%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.7134 71.34%
CYP3A4 inhibition - 0.7477 74.77%
CYP2C9 inhibition - 0.6229 62.29%
CYP2C19 inhibition - 0.5892 58.92%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.7144 71.44%
CYP2C8 inhibition + 0.4843 48.43%
CYP inhibitory promiscuity - 0.7485 74.85%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6267 62.67%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9491 94.91%
Skin irritation - 0.5567 55.67%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis + 0.6117 61.17%
Human Ether-a-go-go-Related Gene inhibition + 0.7244 72.44%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.6263 62.63%
skin sensitisation - 0.6994 69.94%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6440 64.40%
Acute Oral Toxicity (c) I 0.4150 41.50%
Estrogen receptor binding + 0.6709 67.09%
Androgen receptor binding + 0.7528 75.28%
Thyroid receptor binding + 0.6695 66.95%
Glucocorticoid receptor binding + 0.7340 73.40%
Aromatase binding + 0.6368 63.68%
PPAR gamma + 0.5946 59.46%
Honey bee toxicity - 0.6484 64.84%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9860 98.60%

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 98.97% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.13% 91.11%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 94.63% 89.05%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.13% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.00% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.46% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.33% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 92.07% 95.89%
CHEMBL2179 P04062 Beta-glucocerebrosidase 90.27% 85.31%
CHEMBL3837 P07711 Cathepsin L 89.74% 96.61%
CHEMBL2094135 Q96BI3 Gamma-secretase 88.60% 98.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.60% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.33% 96.77%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.25% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 87.54% 90.17%
CHEMBL2581 P07339 Cathepsin D 87.21% 98.95%
CHEMBL237 P41145 Kappa opioid receptor 85.81% 98.10%
CHEMBL226 P30542 Adenosine A1 receptor 85.22% 95.93%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.12% 97.14%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.82% 96.21%
CHEMBL1871 P10275 Androgen Receptor 83.61% 96.43%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.91% 95.50%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.82% 91.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.47% 93.56%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.91% 94.78%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.55% 93.04%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.48% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.28% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.08% 90.71%
CHEMBL344 Q99705 Melanin-concentrating hormone receptor 1 80.08% 92.50%

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.
Ageratina sternbergiana
Astragalus sevangensis
Citrus × aurantium
Cleome dodecandra
Elsholtzia blanda
Prunus tomentosa

Cross-Links

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PubChem 11732746
NPASS NPC65225
LOTUS LTS0244980
wikiData Q105328027