(12Z)-Labda-8(20),12,14-triene

Details

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Internal ID 84fa9e55-bf92-48d9-b98e-b86ffa525b52
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,8S,8aS)-4,4,8a-trimethyl-7-methylidene-8-[(2Z)-3-methylpenta-2,4-dienyl]-2,3,4a,5,6,8-hexahydro-1H-naphthalene
SMILES (Canonical) CC(=CCC1C(=C)CCC2C1(CCCC2(C)C)C)C=C
SMILES (Isomeric) C/C(=C/C[C@H]1C(=C)CC[C@@H]2[C@@]1(CCCC2(C)C)C)/C=C
InChI InChI=1S/C20H32/c1-7-15(2)9-11-17-16(3)10-12-18-19(4,5)13-8-14-20(17,18)6/h7,9,17-18H,1,3,8,10-14H2,2,4-6H3/b15-9-/t17-,18-,20+/m0/s1
InChI Key VJVMMXUPZGOBSN-LZCWJKKXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.20
Atomic LogP (AlogP) 6.31
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (12Z)-Labda-8(20),12,14-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8370 83.70%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.6232 62.32%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.8594 85.94%
OATP1B3 inhibitior - 0.2392 23.92%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5333 53.33%
P-glycoprotein inhibitior - 0.8135 81.35%
P-glycoprotein substrate - 0.8552 85.52%
CYP3A4 substrate + 0.6113 61.13%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.7625 76.25%
CYP3A4 inhibition - 0.8148 81.48%
CYP2C9 inhibition - 0.7540 75.40%
CYP2C19 inhibition - 0.6328 63.28%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition - 0.7950 79.50%
CYP2C8 inhibition - 0.6071 60.71%
CYP inhibitory promiscuity + 0.5824 58.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5194 51.94%
Eye corrosion - 0.9512 95.12%
Eye irritation - 0.7638 76.38%
Skin irritation - 0.6835 68.35%
Skin corrosion - 0.9654 96.54%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8857 88.57%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6101 61.01%
skin sensitisation + 0.8377 83.77%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.4621 46.21%
Acute Oral Toxicity (c) III 0.7955 79.55%
Estrogen receptor binding - 0.4880 48.80%
Androgen receptor binding - 0.4857 48.57%
Thyroid receptor binding - 0.5071 50.71%
Glucocorticoid receptor binding + 0.5378 53.78%
Aromatase binding - 0.4883 48.83%
PPAR gamma + 0.6733 67.33%
Honey bee toxicity - 0.8772 87.72%
Biodegradation - 0.6250 62.50%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.44% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.26% 97.25%
CHEMBL1977 P11473 Vitamin D receptor 91.30% 99.43%
CHEMBL1937 Q92769 Histone deacetylase 2 87.73% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.07% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.35% 98.95%
CHEMBL233 P35372 Mu opioid receptor 84.15% 97.93%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.10% 82.69%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.33% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.77% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.82% 94.45%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 81.04% 100.00%

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.
Ichthyothere terminalis

Cross-Links

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PubChem 12300137
LOTUS LTS0107805
wikiData Q105287542