20beta-Hydroxy-1-oxo-(22R)-witha-2,5,24-trienolide

Details

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Internal ID 39d0d810-2779-4b4b-997d-bb3c95797e6d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (2R)-2-[(1R)-1-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-1-oxo-4,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-1-hydroxyethyl]-4,5-dimethyl-2,3-dihydropyran-6-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC=C5C4(C(=O)C=CC5)C)C)O)C
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@@](C)([C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(C(=O)C=CC5)C)C)O)C
InChI InChI=1S/C28H38O4/c1-16-15-24(32-25(30)17(16)2)28(5,31)22-12-11-20-19-10-9-18-7-6-8-23(29)27(18,4)21(19)13-14-26(20,22)3/h6,8-9,19-22,24,31H,7,10-15H2,1-5H3/t19-,20-,21-,22-,24+,26-,27-,28+/m0/s1
InChI Key VOFPJACKXWOYES-ZJOYFJNASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H38O4
Molecular Weight 438.60 g/mol
Exact Mass 438.27700969 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 4.90
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEMBL2425272
(22R)-20-hydroxy-22,26-epoxyergosta-2,5,24-triene-1,26-dione
6-[1-(10,13-Dimethyl-1-oxo-4,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-1-hydroxy-ethyl]-3,4-dimethyl-5,6-dihydro-pyran-2-one
InChI=1/C28H38O4/c1-16-15-24(32-25(30)17(16)2)28(5,31)22-12-11-20-19-10-9-18-7-6-8-23(29)27(18,4)21(19)13-14-26(20,22)3/h6,8-9,19-22,24,31H,7,10-15H2,1-5H3/t19-,20-,21-,22-,24+,26-,27-,28+/m0/s

2D Structure

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2D Structure of 20beta-Hydroxy-1-oxo-(22R)-witha-2,5,24-trienolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8240 82.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8984 89.84%
OATP1B3 inhibitior + 0.8735 87.35%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5376 53.76%
BSEP inhibitior + 0.9402 94.02%
P-glycoprotein inhibitior + 0.7817 78.17%
P-glycoprotein substrate - 0.5425 54.25%
CYP3A4 substrate + 0.7510 75.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9160 91.60%
CYP3A4 inhibition - 0.8285 82.85%
CYP2C9 inhibition - 0.9354 93.54%
CYP2C19 inhibition - 0.9210 92.10%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition - 0.6375 63.75%
CYP2C8 inhibition + 0.5255 52.55%
CYP inhibitory promiscuity - 0.9606 96.06%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6348 63.48%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.9715 97.15%
Skin irritation + 0.6727 67.27%
Skin corrosion - 0.9073 90.73%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8481 84.81%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8094 80.94%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5116 51.16%
Acute Oral Toxicity (c) IV 0.5217 52.17%
Estrogen receptor binding + 0.8482 84.82%
Androgen receptor binding + 0.7686 76.86%
Thyroid receptor binding + 0.6570 65.70%
Glucocorticoid receptor binding + 0.8665 86.65%
Aromatase binding + 0.7242 72.42%
PPAR gamma + 0.7022 70.22%
Honey bee toxicity - 0.8518 85.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9886 98.86%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.07% 97.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.74% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.05% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.91% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.69% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.70% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 86.70% 94.73%
CHEMBL1871 P10275 Androgen Receptor 86.06% 96.43%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.96% 94.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.64% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.34% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.23% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.07% 85.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.15% 93.04%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.11% 93.40%

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.
Withania coagulans

Cross-Links

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PubChem 637266
LOTUS LTS0176444
wikiData Q104888507