[(1R,2S,3S,4R,5R,7S,8S,9S,10S,11R,12R,14S,15S)-2,12-diacetyloxy-8-benzoyloxy-7-hydroxy-5,9,12-trimethyl-16-oxo-4-propanoyloxy-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-15-yl] benzoate

Details

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Internal ID 1c00ef1f-7a51-471e-96e7-5f2459e2ab24
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(1R,2S,3S,4R,5R,7S,8S,9S,10S,11R,12R,14S,15S)-2,12-diacetyloxy-8-benzoyloxy-7-hydroxy-5,9,12-trimethyl-16-oxo-4-propanoyloxy-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-15-yl] benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H46O13/c1-7-27(44)51-30-21(2)18-41(48)29(30)34(50-22(3)42)40-20-49-39(6,37(41)53-36(47)25-16-12-9-13-17-25)32(40)28-26(19-38(28,5)54-23(4)43)31(33(40)45)52-35(46)24-14-10-8-11-15-24/h8-17,21,26,28-32,34,37,48H,7,18-20H2,1-6H3/t21-,26+,28-,29+,30-,31+,32-,34+,37-,38-,39+,40-,41+/m1/s1
InChI Key JTZAUNVKXSNBLA-GEFIIKTASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C41H46O13
Molecular Weight 746.80 g/mol
Exact Mass 746.29384152 g/mol
Topological Polar Surface Area (TPSA) 178.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 13
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2S,3S,4R,5R,7S,8S,9S,10S,11R,12R,14S,15S)-2,12-diacetyloxy-8-benzoyloxy-7-hydroxy-5,9,12-trimethyl-16-oxo-4-propanoyloxy-18-oxapentacyclo[7.7.2.01,10.03,7.011,14]octadecan-15-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 + 0.9899 98.99%
Caco-2 - 0.8319 83.19%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5083 50.83%
OATP2B1 inhibitior - 0.7173 71.73%
OATP1B1 inhibitior + 0.8399 83.99%
OATP1B3 inhibitior + 0.8702 87.02%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9962 99.62%
P-glycoprotein inhibitior + 0.8800 88.00%
P-glycoprotein substrate + 0.7137 71.37%
CYP3A4 substrate + 0.6940 69.40%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.8549 85.49%
CYP3A4 inhibition - 0.6879 68.79%
CYP2C9 inhibition - 0.7180 71.80%
CYP2C19 inhibition - 0.7622 76.22%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition - 0.7508 75.08%
CYP2C8 inhibition + 0.7864 78.64%
CYP inhibitory promiscuity - 0.8454 84.54%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5139 51.39%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9094 90.94%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7462 74.62%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8225 82.25%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7490 74.90%
Acute Oral Toxicity (c) III 0.5553 55.53%
Estrogen receptor binding + 0.7970 79.70%
Androgen receptor binding + 0.7374 73.74%
Thyroid receptor binding + 0.6026 60.26%
Glucocorticoid receptor binding + 0.7432 74.32%
Aromatase binding + 0.6456 64.56%
PPAR gamma + 0.7632 76.32%
Honey bee toxicity - 0.6619 66.19%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9864 98.64%

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
CHEMBL2581 P07339 Cathepsin D 96.89% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.60% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.93% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.62% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.34% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 93.66% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.80% 99.23%
CHEMBL4040 P28482 MAP kinase ERK2 86.53% 83.82%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.80% 89.34%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.96% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.28% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.30% 97.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.91% 81.11%
CHEMBL5028 O14672 ADAM10 82.80% 97.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.07% 97.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.42% 91.07%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.21% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.66% 93.00%

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.
Euphorbia prolifera

Cross-Links

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PubChem 162884347
LOTUS LTS0060097
wikiData Q105135091