[6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate

Details

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Internal ID 34e20dbd-861c-4875-9982-ddef7e831e8a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name [6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate
SMILES (Canonical) CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)CO)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C
SMILES (Isomeric) CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)CO)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C
InChI InChI=1S/C38H44O12/c1-7-36(6)19-25(49-32(43)23-14-10-8-11-15-23)29-37(20-39)26(18-27(42)38(29,46)34(36)45)35(4,5)30(48-22(3)41)28(47-21(2)40)31(37)50-33(44)24-16-12-9-13-17-24/h7-17,25-31,39,42,46H,1,18-20H2,2-6H3
InChI Key XYELSYGEQPFQMP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C38H44O12
Molecular Weight 692.70 g/mol
Exact Mass 692.28327683 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9699 96.99%
Caco-2 - 0.8308 83.08%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8332 83.32%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8665 86.65%
OATP1B3 inhibitior + 0.8550 85.50%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9949 99.49%
P-glycoprotein inhibitior + 0.8368 83.68%
P-glycoprotein substrate - 0.5453 54.53%
CYP3A4 substrate + 0.6928 69.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8748 87.48%
CYP3A4 inhibition + 0.7201 72.01%
CYP2C9 inhibition - 0.8166 81.66%
CYP2C19 inhibition - 0.7917 79.17%
CYP2D6 inhibition - 0.9442 94.42%
CYP1A2 inhibition - 0.6724 67.24%
CYP2C8 inhibition + 0.5679 56.79%
CYP inhibitory promiscuity - 0.9479 94.79%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7101 71.01%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.9037 90.37%
Skin irritation - 0.7202 72.02%
Skin corrosion - 0.9588 95.88%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8289 82.89%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5473 54.73%
skin sensitisation - 0.8336 83.36%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4763 47.63%
Acute Oral Toxicity (c) III 0.6225 62.25%
Estrogen receptor binding + 0.7926 79.26%
Androgen receptor binding + 0.7158 71.58%
Thyroid receptor binding + 0.6482 64.82%
Glucocorticoid receptor binding + 0.7524 75.24%
Aromatase binding + 0.5982 59.82%
PPAR gamma + 0.7097 70.97%
Honey bee toxicity - 0.6957 69.57%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.20% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 96.43% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.07% 86.33%
CHEMBL2581 P07339 Cathepsin D 96.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.93% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 95.56% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.22% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.89% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.81% 94.62%
CHEMBL340 P08684 Cytochrome P450 3A4 89.09% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.04% 82.69%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.22% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.62% 95.50%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 84.39% 94.08%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.58% 97.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.52% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.19% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.34% 100.00%

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.
Orthosiphon aristatus var. aristatus

Cross-Links

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PubChem 74821602
LOTUS LTS0200840
wikiData Q105344450