3beta,14beta-Dihydroxyergosta-5,8,22-trien-7-one

Details

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Internal ID 439c91bd-8d08-4f9a-94ee-434f101d1baa
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Ergostane steroids > Ergosterols and derivatives
IUPAC Name (3S,10S,13R,14R,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-3,14-dihydroxy-10,13-dimethyl-2,3,4,11,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H42O3/c1-17(2)18(3)7-8-19(4)22-11-14-28(31)25-23(10-13-27(22,28)6)26(5)12-9-21(29)15-20(26)16-24(25)30/h7-8,16-19,21-22,29,31H,9-15H2,1-6H3/b8-7+/t18-,19+,21-,22+,26-,27+,28-/m0/s1
InChI Key NWWFNBWEOSOPAK-LRARISCQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H42O3
Molecular Weight 426.60 g/mol
Exact Mass 426.31339520 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.77
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3beta,14beta-Dihydroxyergosta-5,8,22-trien-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 + 0.6620 66.20%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7928 79.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7872 78.72%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior + 0.9340 93.40%
P-glycoprotein inhibitior - 0.4391 43.91%
P-glycoprotein substrate - 0.5457 54.57%
CYP3A4 substrate + 0.6811 68.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8962 89.62%
CYP3A4 inhibition - 0.8943 89.43%
CYP2C9 inhibition - 0.8581 85.81%
CYP2C19 inhibition - 0.8436 84.36%
CYP2D6 inhibition - 0.9579 95.79%
CYP1A2 inhibition - 0.8736 87.36%
CYP2C8 inhibition - 0.6338 63.38%
CYP inhibitory promiscuity - 0.8307 83.07%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Warning 0.4607 46.07%
Eye corrosion - 0.9943 99.43%
Eye irritation - 0.9563 95.63%
Skin irritation + 0.6569 65.69%
Skin corrosion - 0.9550 95.50%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5788 57.88%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5428 54.28%
skin sensitisation - 0.6091 60.91%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity - 0.7633 76.33%
Acute Oral Toxicity (c) I 0.6956 69.56%
Estrogen receptor binding + 0.8234 82.34%
Androgen receptor binding + 0.7550 75.50%
Thyroid receptor binding + 0.7223 72.23%
Glucocorticoid receptor binding + 0.7389 73.89%
Aromatase binding + 0.6469 64.69%
PPAR gamma + 0.6229 62.29%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9920 99.20%

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
CHEMBL2581 P07339 Cathepsin D 98.37% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.72% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.03% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.19% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 92.68% 95.93%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.98% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.85% 85.14%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.83% 93.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.67% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.38% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.99% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.71% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.38% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.14% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.48% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.30% 99.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.89% 93.56%
CHEMBL1951 P21397 Monoamine oxidase A 81.94% 91.49%

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 139591408
LOTUS LTS0205496
wikiData Q105186835