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

Details

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Internal ID 5cb93e67-9024-47ab-89eb-97691f878e68
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name [(1S,3R,5S,6aS,7R,8R,10S,10aS)-1,3-diacetyloxy-10-hydroxy-7,8-dimethyl-7-[(2Z)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] 2-methylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H40O8/c1-9-16(4)10-11-27(8)17(5)12-23(31)28-21(13-20(14-22(27)28)35-24(32)15(2)3)25(33-18(6)29)36-26(28)34-19(7)30/h9-10,13,15,17,20,22-23,25-26,31H,1,11-12,14H2,2-8H3/b16-10-/t17-,20-,22+,23+,25+,26-,27-,28-/m1/s1
InChI Key PASSAFHUDJPXAL-RGJUMIETSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O8
Molecular Weight 504.60 g/mol
Exact Mass 504.27231823 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.22
H-Bond Acceptor 8
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,3R,5S,6aS,7R,8R,10S,10aS)-1,3-diacetyloxy-10-hydroxy-7,8-dimethyl-7-[(2Z)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] 2-methylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 - 0.6722 67.22%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6971 69.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8588 85.88%
OATP1B3 inhibitior - 0.2827 28.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8409 84.09%
P-glycoprotein inhibitior + 0.7525 75.25%
P-glycoprotein substrate - 0.5411 54.11%
CYP3A4 substrate + 0.6850 68.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8630 86.30%
CYP3A4 inhibition + 0.6958 69.58%
CYP2C9 inhibition - 0.7991 79.91%
CYP2C19 inhibition - 0.8122 81.22%
CYP2D6 inhibition - 0.9549 95.49%
CYP1A2 inhibition - 0.7703 77.03%
CYP2C8 inhibition + 0.5423 54.23%
CYP inhibitory promiscuity - 0.7912 79.12%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5392 53.92%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.8914 89.14%
Skin irritation + 0.5637 56.37%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3871 38.71%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7435 74.35%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.5178 51.78%
Acute Oral Toxicity (c) I 0.6057 60.57%
Estrogen receptor binding + 0.7885 78.85%
Androgen receptor binding + 0.6582 65.82%
Thyroid receptor binding + 0.5772 57.72%
Glucocorticoid receptor binding + 0.8023 80.23%
Aromatase binding + 0.6586 65.86%
PPAR gamma + 0.7138 71.38%
Honey bee toxicity - 0.6910 69.10%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6300 63.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.35% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.73% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.63% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.10% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.94% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.49% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 86.26% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.87% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.78% 97.25%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.40% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.28% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.88% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.86% 91.19%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.66% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.44% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.28% 95.56%
CHEMBL5028 O14672 ADAM10 80.97% 97.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.42% 99.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.39% 96.77%

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 sylvestris

Cross-Links

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PubChem 15538078
LOTUS LTS0173105
wikiData Q105204726