(10-acetyloxy-5-benzoyloxy-2-ethenyl-6,7,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate

Details

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Internal ID b74d5f18-f875-48a7-9980-b75720ef6518
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (10-acetyloxy-5-benzoyloxy-2-ethenyl-6,7,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate
SMILES (Canonical) CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C
SMILES (Isomeric) CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C
InChI InChI=1S/C36H42O10/c1-7-34(5)19-23(45-30(40)21-14-10-8-11-15-21)27-35(6)24(18-25(44-20(2)37)36(27,43)32(34)42)33(3,4)28(39)26(38)29(35)46-31(41)22-16-12-9-13-17-22/h7-17,23-29,38-39,43H,1,18-19H2,2-6H3
InChI Key XZOHHNDEJRVJSL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H42O10
Molecular Weight 634.70 g/mol
Exact Mass 634.27779753 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (10-acetyloxy-5-benzoyloxy-2-ethenyl-6,7,10a-trihydroxy-2,4b,8,8-tetramethyl-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 + 0.9710 97.10%
Caco-2 - 0.8101 81.01%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7294 72.94%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8882 88.82%
OATP1B3 inhibitior + 0.8402 84.02%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9499 94.99%
P-glycoprotein inhibitior + 0.8051 80.51%
P-glycoprotein substrate - 0.6056 60.56%
CYP3A4 substrate + 0.6718 67.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8702 87.02%
CYP3A4 inhibition + 0.5401 54.01%
CYP2C9 inhibition - 0.8464 84.64%
CYP2C19 inhibition - 0.8405 84.05%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.6552 65.52%
CYP2C8 inhibition + 0.6972 69.72%
CYP inhibitory promiscuity - 0.9385 93.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.5733 57.33%
Eye corrosion - 0.9932 99.32%
Eye irritation - 0.9059 90.59%
Skin irritation - 0.7103 71.03%
Skin corrosion - 0.9267 92.67%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7576 75.76%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6966 69.66%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6449 64.49%
Acute Oral Toxicity (c) III 0.6312 63.12%
Estrogen receptor binding + 0.7250 72.50%
Androgen receptor binding + 0.6624 66.24%
Thyroid receptor binding + 0.6163 61.63%
Glucocorticoid receptor binding + 0.7445 74.45%
Aromatase binding + 0.6023 60.23%
PPAR gamma + 0.6829 68.29%
Honey bee toxicity - 0.6859 68.59%
Biodegradation - 0.8500 85.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.79% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 95.73% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.08% 86.33%
CHEMBL2581 P07339 Cathepsin D 94.84% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.76% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 91.29% 91.19%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.12% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 89.94% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.67% 99.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.51% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 87.90% 94.08%
CHEMBL2535 P11166 Glucose transporter 86.13% 98.75%
CHEMBL240 Q12809 HERG 85.36% 89.76%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.30% 95.50%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 83.54% 83.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.14% 97.14%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.77% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.53% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.45% 82.69%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.32% 85.14%
CHEMBL5028 O14672 ADAM10 82.30% 97.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.41% 91.07%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 80.67% 97.53%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.62% 96.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.33% 95.89%

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.
Catoferia spicata
Orthosiphon aristatus
Orthosiphon aristatus var. aristatus

Cross-Links

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PubChem 85105215
LOTUS LTS0126035
wikiData Q105345074