[(1S,2S,4aR,4bS,8S,8aS,9S,10aR)-2,9-diacetyloxy-7-ethenyl-8-hydroxy-1,4a,8-trimethyl-3,4,4b,5,8a,9,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate

Details

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Internal ID 733530fc-bc86-49b0-9ce0-f953eaf0f9bc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Isocopalane and spongiane diterpenoids
IUPAC Name [(1S,2S,4aR,4bS,8S,8aS,9S,10aR)-2,9-diacetyloxy-7-ethenyl-8-hydroxy-1,4a,8-trimethyl-3,4,4b,5,8a,9,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate
SMILES (Canonical) CC(=O)OCC1(C(CCC2(C1CC(C3C2CC=C(C3(C)O)C=C)OC(=O)C)C)OC(=O)C)C
SMILES (Isomeric) CC(=O)OC[C@]1([C@H](CC[C@]2([C@H]1C[C@@H]([C@@H]3[C@@H]2CC=C([C@@]3(C)O)C=C)OC(=O)C)C)OC(=O)C)C
InChI InChI=1S/C26H38O7/c1-8-18-9-10-19-23(26(18,7)30)20(32-16(3)28)13-21-24(19,5)12-11-22(33-17(4)29)25(21,6)14-31-15(2)27/h8-9,19-23,30H,1,10-14H2,2-7H3/t19-,20-,21+,22-,23-,24+,25+,26+/m0/s1
InChI Key SGFRXWGRPVRKAX-WUZRRLPESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H38O7
Molecular Weight 462.60 g/mol
Exact Mass 462.26175355 g/mol
Topological Polar Surface Area (TPSA) 99.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,4aR,4bS,8S,8aS,9S,10aR)-2,9-diacetyloxy-7-ethenyl-8-hydroxy-1,4a,8-trimethyl-3,4,4b,5,8a,9,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 - 0.6425 64.25%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8438 84.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8512 85.12%
OATP1B3 inhibitior + 0.8794 87.94%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6271 62.71%
BSEP inhibitior + 0.9627 96.27%
P-glycoprotein inhibitior + 0.6313 63.13%
P-glycoprotein substrate - 0.6988 69.88%
CYP3A4 substrate + 0.6947 69.47%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8907 89.07%
CYP3A4 inhibition - 0.7025 70.25%
CYP2C9 inhibition - 0.8503 85.03%
CYP2C19 inhibition - 0.8542 85.42%
CYP2D6 inhibition - 0.9467 94.67%
CYP1A2 inhibition - 0.6136 61.36%
CYP2C8 inhibition + 0.5894 58.94%
CYP inhibitory promiscuity - 0.8875 88.75%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6336 63.36%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9009 90.09%
Skin irritation + 0.5998 59.98%
Skin corrosion - 0.9707 97.07%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3892 38.92%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5952 59.52%
skin sensitisation - 0.8430 84.30%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5854 58.54%
Acute Oral Toxicity (c) III 0.8163 81.63%
Estrogen receptor binding + 0.8399 83.99%
Androgen receptor binding + 0.5905 59.05%
Thyroid receptor binding + 0.5735 57.35%
Glucocorticoid receptor binding + 0.8043 80.43%
Aromatase binding + 0.7061 70.61%
PPAR gamma + 0.7045 70.45%
Honey bee toxicity - 0.7144 71.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5200 52.00%
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 97.43% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.56% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.45% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.07% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.49% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.74% 82.69%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.64% 94.62%
CHEMBL340 P08684 Cytochrome P450 3A4 89.43% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.30% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.10% 97.09%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 88.99% 91.65%
CHEMBL5028 O14672 ADAM10 86.88% 97.50%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.26% 94.08%
CHEMBL2581 P07339 Cathepsin D 85.68% 98.95%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 85.67% 94.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.58% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.14% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.85% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.81% 91.07%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.77% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.22% 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.
Dendrolirium tomentosum
Eucalyptus froggattii
Pistacia mexicana

Cross-Links

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PubChem 10813923
NPASS NPC201742