[(1S,2R,4S,6S,7S,8R,9S,10S,11R,12S,13R)-6,7-diacetyloxy-8-benzoyloxy-12-ethenyl-2-hydroxy-5,5,9,13-tetramethyl-14-oxo-15,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadecan-11-yl] benzoate

Details

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Internal ID 1db7d736-267b-40ee-ac65-dfe80685c1ed
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(1S,2R,4S,6S,7S,8R,9S,10S,11R,12S,13R)-6,7-diacetyloxy-8-benzoyloxy-12-ethenyl-2-hydroxy-5,5,9,13-tetramethyl-14-oxo-15,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadecan-11-yl] benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H42O12/c1-8-24-27(47-32(42)22-15-11-9-12-16-22)29-36(6)25(19-26(41)38(29)49-34(44)37(24,7)50-38)35(4,5)30(46-21(3)40)28(45-20(2)39)31(36)48-33(43)23-17-13-10-14-18-23/h8-18,24-31,41H,1,19H2,2-7H3/t24-,25-,26+,27+,28-,29+,30+,31-,36-,37+,38-/m0/s1
InChI Key RNTVZXREBCHYPP-CWUCWMPNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C38H42O12
Molecular Weight 690.70 g/mol
Exact Mass 690.26762677 g/mol
Topological Polar Surface Area (TPSA) 161.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 12
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,4S,6S,7S,8R,9S,10S,11R,12S,13R)-6,7-diacetyloxy-8-benzoyloxy-12-ethenyl-2-hydroxy-5,5,9,13-tetramethyl-14-oxo-15,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadecan-11-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 + 0.9791 97.91%
Caco-2 - 0.8122 81.22%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6172 61.72%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.8365 83.65%
OATP1B3 inhibitior - 0.2345 23.45%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9800 98.00%
P-glycoprotein inhibitior + 0.8711 87.11%
P-glycoprotein substrate - 0.6058 60.58%
CYP3A4 substrate + 0.6890 68.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8572 85.72%
CYP3A4 inhibition + 0.7024 70.24%
CYP2C9 inhibition - 0.9495 94.95%
CYP2C19 inhibition - 0.8889 88.89%
CYP2D6 inhibition - 0.9076 90.76%
CYP1A2 inhibition - 0.9200 92.00%
CYP2C8 inhibition + 0.7100 71.00%
CYP inhibitory promiscuity - 0.9346 93.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.4247 42.47%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8901 89.01%
Skin irritation - 0.7147 71.47%
Skin corrosion - 0.9003 90.03%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7048 70.48%
Micronuclear + 0.5359 53.59%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6970 69.70%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5462 54.62%
Acute Oral Toxicity (c) III 0.4801 48.01%
Estrogen receptor binding + 0.7595 75.95%
Androgen receptor binding + 0.6687 66.87%
Thyroid receptor binding + 0.6580 65.80%
Glucocorticoid receptor binding + 0.7431 74.31%
Aromatase binding + 0.5820 58.20%
PPAR gamma + 0.7333 73.33%
Honey bee toxicity - 0.6613 66.13%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9887 98.87%

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
CHEMBL240 Q12809 HERG 99.90% 89.76%
CHEMBL1951 P21397 Monoamine oxidase A 98.73% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 98.52% 90.17%
CHEMBL2581 P07339 Cathepsin D 96.83% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.95% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.49% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.06% 91.07%
CHEMBL340 P08684 Cytochrome P450 3A4 88.83% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.52% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.51% 99.23%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 88.46% 83.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.39% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.11% 95.50%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.61% 94.08%
CHEMBL5028 O14672 ADAM10 80.74% 97.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.50% 95.89%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.47% 94.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.33% 97.14%

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 162892710
LOTUS LTS0219695
wikiData Q105241836