methyl (1aS,4S,4aS,7R,8R,8aR)-7-[(1R,6R)-6-(acetyloxymethyl)-1,5,5-trimethyl-4-oxocyclohex-2-en-1-yl]-4-(furan-3-yl)-4a,8-dimethyl-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromene-8-carboxylate

Details

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Internal ID b5141f5e-9824-4dc3-8823-9575793e6ef2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name methyl (1aS,4S,4aS,7R,8R,8aR)-7-[(1R,6R)-6-(acetyloxymethyl)-1,5,5-trimethyl-4-oxocyclohex-2-en-1-yl]-4-(furan-3-yl)-4a,8-dimethyl-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromene-8-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H36O9/c1-16(30)36-15-19-25(2,3)20(31)9-11-26(19,4)18-8-12-27(5)21(17-10-13-35-14-17)37-23(32)22-29(27,38-22)28(18,6)24(33)34-7/h9-11,13-14,18-19,21-22H,8,12,15H2,1-7H3/t18-,19+,21+,22-,26-,27+,28+,29-/m1/s1
InChI Key PTLZHOLOQAFTMS-SCXLJDOTSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C29H36O9
Molecular Weight 528.60 g/mol
Exact Mass 528.23593272 g/mol
Topological Polar Surface Area (TPSA) 122.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.96
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1aS,4S,4aS,7R,8R,8aR)-7-[(1R,6R)-6-(acetyloxymethyl)-1,5,5-trimethyl-4-oxocyclohex-2-en-1-yl]-4-(furan-3-yl)-4a,8-dimethyl-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromene-8-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 - 0.7043 70.43%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7722 77.22%
OATP2B1 inhibitior - 0.7198 71.98%
OATP1B1 inhibitior - 0.4378 43.78%
OATP1B3 inhibitior + 0.8801 88.01%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9673 96.73%
P-glycoprotein inhibitior + 0.8696 86.96%
P-glycoprotein substrate + 0.5274 52.74%
CYP3A4 substrate + 0.7108 71.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8776 87.76%
CYP3A4 inhibition + 0.6681 66.81%
CYP2C9 inhibition - 0.6538 65.38%
CYP2C19 inhibition - 0.6903 69.03%
CYP2D6 inhibition - 0.8977 89.77%
CYP1A2 inhibition - 0.8040 80.40%
CYP2C8 inhibition + 0.7281 72.81%
CYP inhibitory promiscuity - 0.6478 64.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5730 57.30%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.8438 84.38%
Skin irritation - 0.7586 75.86%
Skin corrosion - 0.9289 92.89%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7796 77.96%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.5789 57.89%
skin sensitisation - 0.8084 80.84%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6344 63.44%
Acute Oral Toxicity (c) I 0.4386 43.86%
Estrogen receptor binding + 0.8572 85.72%
Androgen receptor binding + 0.7755 77.55%
Thyroid receptor binding + 0.7204 72.04%
Glucocorticoid receptor binding + 0.8724 87.24%
Aromatase binding + 0.7409 74.09%
PPAR gamma + 0.7442 74.42%
Honey bee toxicity - 0.8358 83.58%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.74% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.71% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.24% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.90% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.13% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.00% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.40% 94.00%
CHEMBL2581 P07339 Cathepsin D 85.04% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 84.49% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.10% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.14% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.92% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.84% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.91% 82.69%
CHEMBL255 P29275 Adenosine A2b receptor 80.61% 98.59%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.13% 93.04%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.01% 97.28%

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.
Swietenia macrophylla
Swietenia mahagoni

Cross-Links

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PubChem 21636292
LOTUS LTS0119978
wikiData Q104396484