[(1S,3R,5R,6aS,7S,8S,9R,10S,10aS)-1,3-diacetyloxy-9,10-dihydroxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] (4E)-deca-2,4-dienoate

Details

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Internal ID 1021a022-e74c-4a4c-a895-748f148ccd92
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name [(1S,3R,5R,6aS,7S,8S,9R,10S,10aS)-1,3-diacetyloxy-9,10-dihydroxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] (4E)-deca-2,4-dienoate
SMILES (Canonical) CCCCCC=CC=CC(=O)OC1CC2C(C(C(C(C23C(OC(C3=C1)OC(=O)C)OC(=O)C)O)O)C)(C)CC=C(C)C=C
SMILES (Isomeric) CCCCC/C=C/C=CC(=O)O[C@@H]1C[C@H]2[C@]([C@@H]([C@H]([C@H]([C@]23[C@@H](O[C@@H](C3=C1)OC(=O)C)OC(=O)C)O)O)C)(C)C/C=C(\C)/C=C
InChI InChI=1S/C34H48O9/c1-8-10-11-12-13-14-15-16-28(37)42-25-19-26-31(40-23(5)35)43-32(41-24(6)36)34(26)27(20-25)33(7,18-17-21(3)9-2)22(4)29(38)30(34)39/h9,13-17,19,22,25,27,29-32,38-39H,2,8,10-12,18,20H2,1,3-7H3/b14-13+,16-15?,21-17+/t22-,25+,27+,29-,30-,31+,32-,33-,34-/m1/s1
InChI Key SYVLIZAFBWNVCK-KPGGFAJMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H48O9
Molecular Weight 600.70 g/mol
Exact Mass 600.32983310 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.23
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,3R,5R,6aS,7S,8S,9R,10S,10aS)-1,3-diacetyloxy-9,10-dihydroxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] (4E)-deca-2,4-dienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9713 97.13%
Caco-2 - 0.8235 82.35%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6201 62.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7866 78.66%
OATP1B3 inhibitior + 0.8713 87.13%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9539 95.39%
P-glycoprotein inhibitior + 0.7841 78.41%
P-glycoprotein substrate + 0.6147 61.47%
CYP3A4 substrate + 0.7135 71.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8869 88.69%
CYP3A4 inhibition + 0.7556 75.56%
CYP2C9 inhibition - 0.6692 66.92%
CYP2C19 inhibition - 0.6516 65.16%
CYP2D6 inhibition - 0.9033 90.33%
CYP1A2 inhibition + 0.5293 52.93%
CYP2C8 inhibition + 0.7150 71.50%
CYP inhibitory promiscuity - 0.7173 71.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.4614 46.14%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9135 91.35%
Skin irritation + 0.6477 64.77%
Skin corrosion - 0.8981 89.81%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7972 79.72%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8487 84.87%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.5177 51.77%
Acute Oral Toxicity (c) III 0.5337 53.37%
Estrogen receptor binding + 0.7553 75.53%
Androgen receptor binding + 0.6920 69.20%
Thyroid receptor binding + 0.5464 54.64%
Glucocorticoid receptor binding + 0.7114 71.14%
Aromatase binding + 0.6016 60.16%
PPAR gamma + 0.6884 68.84%
Honey bee toxicity - 0.7800 78.00%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5753 57.53%
Fish aquatic toxicity + 0.9970 99.70%

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 98.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.75% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.35% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.02% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 93.17% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.04% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.99% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.48% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.56% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.50% 89.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.27% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.62% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.30% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.39% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.91% 92.94%

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.
Casearia arguta

Cross-Links

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PubChem 162983396
LOTUS LTS0154206
wikiData Q105263804