(1R,2R,7R,10R,11S,14R,15S,16R)-7-hydroxy-16-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one

Details

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Internal ID d323fa87-754f-441a-afc1-b73eb24ba425
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (1R,2R,7R,10R,11S,14R,15S,16R)-7-hydroxy-16-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C2(C3CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)C)CO
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@]2([C@H]3CC[C@@]4([C@@]3(CC[C@H]5[C@H]4CC=C6[C@@]5(C(=O)C[C@@H](C6)O)C)C)O2)C)CO
InChI InChI=1S/C28H38O6/c1-15-11-23(33-24(32)18(15)14-29)27(4)21-8-10-28(34-27)20-6-5-16-12-17(30)13-22(31)26(16,3)19(20)7-9-25(21,28)2/h5,17,19-21,23,29-30H,6-14H2,1-4H3/t17-,19+,20-,21+,23-,25-,26+,27-,28-/m1/s1
InChI Key SYAAPYCBHNSHLM-NYNCXJGOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H38O6
Molecular Weight 470.60 g/mol
Exact Mass 470.26683893 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,7R,10R,11S,14R,15S,16R)-7-hydroxy-16-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9668 96.68%
Caco-2 - 0.6561 65.61%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8645 86.45%
OATP2B1 inhibitior - 0.7165 71.65%
OATP1B1 inhibitior + 0.8403 84.03%
OATP1B3 inhibitior + 0.9735 97.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.8652 86.52%
P-glycoprotein inhibitior + 0.5984 59.84%
P-glycoprotein substrate - 0.5709 57.09%
CYP3A4 substrate + 0.6963 69.63%
CYP2C9 substrate - 0.8256 82.56%
CYP2D6 substrate - 0.8948 89.48%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.9417 94.17%
CYP2C19 inhibition - 0.9652 96.52%
CYP2D6 inhibition - 0.9585 95.85%
CYP1A2 inhibition - 0.9082 90.82%
CYP2C8 inhibition + 0.5750 57.50%
CYP inhibitory promiscuity - 0.9269 92.69%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.6662 66.62%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9477 94.77%
Skin irritation + 0.7322 73.22%
Skin corrosion - 0.9300 93.00%
Ames mutagenesis - 0.5970 59.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4528 45.28%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5964 59.64%
skin sensitisation - 0.9300 93.00%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.6446 64.46%
Acute Oral Toxicity (c) I 0.5631 56.31%
Estrogen receptor binding + 0.8354 83.54%
Androgen receptor binding + 0.7802 78.02%
Thyroid receptor binding - 0.5230 52.30%
Glucocorticoid receptor binding + 0.8231 82.31%
Aromatase binding + 0.7594 75.94%
PPAR gamma + 0.6314 63.14%
Honey bee toxicity - 0.8052 80.52%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9673 96.73%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.61% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.21% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 90.76% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.89% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.14% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.93% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.79% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 88.05% 93.03%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.32% 93.04%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.22% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.86% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.96% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.80% 94.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.95% 90.08%
CHEMBL5028 O14672 ADAM10 80.34% 97.50%

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.
Ajuga parviflora
Withania coagulans

Cross-Links

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PubChem 15968792
LOTUS LTS0190596
wikiData Q105263434