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

Details

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Internal ID 80e3c945-45ec-4f1e-bdd3-66b4949fc5f2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name [(3R,5R,6aS,7R,8R,10S,10aS)-1,3-dibutoxy-5-hydroxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-10-yl] acetate
SMILES (Canonical) CCCCOC1C2=CC(CC3C2(C(CC(C3(C)CC=C(C)C=C)C)OC(=O)C)C(O1)OCCCC)O
SMILES (Isomeric) CCCCO[C@H]1C2=C[C@@H](C[C@@H]3[C@]2([C@H](C[C@H]([C@@]3(C)C/C=C(\C)/C=C)C)OC(=O)C)C(O1)OCCCC)O
InChI InChI=1S/C30H48O6/c1-8-11-15-33-27-24-18-23(32)19-25-29(7,14-13-20(4)10-3)21(5)17-26(35-22(6)31)30(24,25)28(36-27)34-16-12-9-2/h10,13,18,21,23,25-28,32H,3,8-9,11-12,14-17,19H2,1-2,4-7H3/b20-13+/t21-,23+,25+,26+,27-,28?,29-,30-/m1/s1
InChI Key VKVRYQDUFKMGCG-FORMUVFOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O6
Molecular Weight 504.70 g/mol
Exact Mass 504.34508925 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 6.10
Atomic LogP (AlogP) 6.10
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 - 0.6314 63.14%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5987 59.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8266 82.66%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9098 90.98%
P-glycoprotein inhibitior + 0.7286 72.86%
P-glycoprotein substrate + 0.5494 54.94%
CYP3A4 substrate + 0.7044 70.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8780 87.80%
CYP3A4 inhibition - 0.5254 52.54%
CYP2C9 inhibition - 0.8023 80.23%
CYP2C19 inhibition - 0.7814 78.14%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.8104 81.04%
CYP2C8 inhibition + 0.6533 65.33%
CYP inhibitory promiscuity - 0.8454 84.54%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5522 55.22%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9363 93.63%
Skin irritation + 0.5805 58.05%
Skin corrosion - 0.9400 94.00%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7665 76.65%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5410 54.10%
skin sensitisation - 0.8644 86.44%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5110 51.10%
Acute Oral Toxicity (c) III 0.6512 65.12%
Estrogen receptor binding + 0.7886 78.86%
Androgen receptor binding + 0.5969 59.69%
Thyroid receptor binding - 0.5914 59.14%
Glucocorticoid receptor binding + 0.7754 77.54%
Aromatase binding + 0.7728 77.28%
PPAR gamma + 0.6933 69.33%
Honey bee toxicity - 0.8100 81.00%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9951 99.51%

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 98.37% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.82% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.83% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.37% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.93% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.23% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.44% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 89.04% 97.79%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.53% 96.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.14% 92.94%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.48% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.35% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 86.34% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 83.96% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.44% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.25% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.07% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.66% 100.00%
CHEMBL4530 P00488 Coagulation factor XIII 81.08% 96.00%
CHEMBL3891 P07384 Calpain 1 80.50% 93.04%
CHEMBL299 P17252 Protein kinase C alpha 80.48% 98.03%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.40% 95.89%

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 101602072
LOTUS LTS0072763
wikiData Q105288126