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

Details

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Internal ID 707f3df1-5728-46fa-96d5-2ee072802259
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name [(5R,6aS,7R,8R,10S,10aS)-1,3-diacetyloxy-7,8-dimethyl-5-(2-methylbutanoyloxy)-7-[(2E)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-10-yl] benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H46O9/c1-9-21(3)16-17-35(8)23(5)18-30(44-32(40)26-14-12-11-13-15-26)36-28(33(41-24(6)37)45-34(36)42-25(7)38)19-27(20-29(35)36)43-31(39)22(4)10-2/h9,11-16,19,22-23,27,29-30,33-34H,1,10,17-18,20H2,2-8H3/b21-16+/t22?,23-,27+,29+,30+,33?,34?,35-,36-/m1/s1
InChI Key FLLKSIKUPUMYAK-LCXPLBHPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C36H46O9
Molecular Weight 622.70 g/mol
Exact Mass 622.31418304 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP 7.30
Atomic LogP (AlogP) 6.48
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(5R,6aS,7R,8R,10S,10aS)-1,3-diacetyloxy-7,8-dimethyl-5-(2-methylbutanoyloxy)-7-[(2E)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-10-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 + 1.0000 100.00%
Caco-2 - 0.7610 76.10%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5037 50.37%
OATP2B1 inhibitior - 0.7182 71.82%
OATP1B1 inhibitior + 0.8196 81.96%
OATP1B3 inhibitior + 0.7892 78.92%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9797 97.97%
P-glycoprotein inhibitior + 0.8988 89.88%
P-glycoprotein substrate + 0.6089 60.89%
CYP3A4 substrate + 0.6926 69.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition + 0.7994 79.94%
CYP2C9 inhibition - 0.7212 72.12%
CYP2C19 inhibition - 0.5362 53.62%
CYP2D6 inhibition - 0.9522 95.22%
CYP1A2 inhibition - 0.5953 59.53%
CYP2C8 inhibition + 0.7468 74.68%
CYP inhibitory promiscuity + 0.5886 58.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5378 53.78%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9101 91.01%
Skin irritation - 0.5829 58.29%
Skin corrosion - 0.9425 94.25%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7185 71.85%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5589 55.89%
skin sensitisation - 0.7360 73.60%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.4621 46.21%
Acute Oral Toxicity (c) III 0.5685 56.85%
Estrogen receptor binding + 0.7463 74.63%
Androgen receptor binding + 0.6922 69.22%
Thyroid receptor binding + 0.5876 58.76%
Glucocorticoid receptor binding + 0.7730 77.30%
Aromatase binding + 0.6000 60.00%
PPAR gamma + 0.7231 72.31%
Honey bee toxicity - 0.7509 75.09%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
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
CHEMBL2581 P07339 Cathepsin D 97.47% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.84% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.15% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.94% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.60% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.99% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 88.81% 97.79%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.31% 95.50%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.15% 90.24%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.83% 97.14%
CHEMBL5028 O14672 ADAM10 84.36% 97.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.24% 99.23%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.65% 94.08%
CHEMBL3401 O75469 Pregnane X receptor 82.58% 94.73%
CHEMBL4208 P20618 Proteasome component C5 82.53% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.45% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 82.30% 91.19%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 82.17% 83.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.96% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.60% 92.62%
CHEMBL3891 P07384 Calpain 1 80.30% 93.04%

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 bicolor

Cross-Links

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PubChem 44404750
LOTUS LTS0036392
wikiData Q104997211