Witharistatin

Details

Top
Internal ID 057406ec-8737-4e39-ad30-a800f122d413
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (1S,2R,6S,7R,9R,11S,12S,16S)-6-hydroxy-15-[(1S)-1-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadeca-4,14-dien-3-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)C2=CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)CO
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@@H](C)C2=CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3C[C@@H]5[C@]6([C@@]4(C(=O)C=C[C@@H]6O)C)O5)C)CO
InChI InChI=1S/C28H36O6/c1-14-11-21(33-25(32)17(14)13-29)15(2)18-5-6-19-16-12-24-28(34-24)23(31)8-7-22(30)27(28,4)20(16)9-10-26(18,19)3/h5,7-8,15-16,19-21,23-24,29,31H,6,9-13H2,1-4H3/t15-,16-,19-,20-,21+,23-,24+,26+,27-,28+/m0/s1
InChI Key UFEAJHDMQVGVJI-NODKRQMBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C28H36O6
Molecular Weight 468.60 g/mol
Exact Mass 468.25118886 g/mol
Topological Polar Surface Area (TPSA) 96.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
CHEMBL2047411

2D Structure

Top
2D Structure of Witharistatin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8983 89.83%
Caco-2 - 0.6332 63.32%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7714 77.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8451 84.51%
OATP1B3 inhibitior + 0.9702 97.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5771 57.71%
BSEP inhibitior + 0.9682 96.82%
P-glycoprotein inhibitior + 0.6993 69.93%
P-glycoprotein substrate + 0.5771 57.71%
CYP3A4 substrate + 0.7020 70.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8921 89.21%
CYP3A4 inhibition - 0.8547 85.47%
CYP2C9 inhibition - 0.8867 88.67%
CYP2C19 inhibition - 0.9390 93.90%
CYP2D6 inhibition - 0.9517 95.17%
CYP1A2 inhibition - 0.7829 78.29%
CYP2C8 inhibition + 0.5335 53.35%
CYP inhibitory promiscuity - 0.9338 93.38%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5377 53.77%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9597 95.97%
Skin irritation + 0.5455 54.55%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6650 66.50%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6064 60.64%
skin sensitisation - 0.8846 88.46%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.6707 67.07%
Acute Oral Toxicity (c) I 0.5780 57.80%
Estrogen receptor binding + 0.8024 80.24%
Androgen receptor binding + 0.7723 77.23%
Thyroid receptor binding + 0.5780 57.80%
Glucocorticoid receptor binding + 0.8640 86.40%
Aromatase binding + 0.6765 67.65%
PPAR gamma + 0.6429 64.29%
Honey bee toxicity - 0.7298 72.98%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9671 96.71%

Targets

Top

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 96.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.56% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.57% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.79% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.61% 97.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.04% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.08% 93.56%
CHEMBL1937 Q92769 Histone deacetylase 2 86.88% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.73% 96.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.10% 90.08%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.52% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 84.29% 97.79%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.74% 88.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.31% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.98% 93.03%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.40% 96.61%
CHEMBL1871 P10275 Androgen Receptor 81.31% 96.43%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.30% 82.69%
CHEMBL3401 O75469 Pregnane X receptor 80.79% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.44% 95.89%

Plants that contains it

Top
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 aristata

Cross-Links

Top
PubChem 70690364
LOTUS LTS0119734
wikiData Q105271474