(-)-Ventricos-7(13)-ene

Details

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Internal ID a97736fb-3ac1-4605-b406-bb5c55f5c854
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Angular triquinanes
IUPAC Name (1S,2S,5S,8S)-2,10,10-trimethyl-7-methylidenetricyclo[6.3.0.01,5]undecane
SMILES (Canonical) CC1CCC2C13CC(CC3C(=C)C2)(C)C
SMILES (Isomeric) C[C@H]1CC[C@@H]2[C@]13CC(C[C@H]3C(=C)C2)(C)C
InChI InChI=1S/C15H24/c1-10-7-12-6-5-11(2)15(12)9-14(3,4)8-13(10)15/h11-13H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m0/s1
InChI Key CPNKKZQGNNFQGD-ABHRYQDASA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.42
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CPNKKZQGNNFQGD-ABHRYQDASA-N

2D Structure

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2D Structure of (-)-Ventricos-7(13)-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.7194 71.94%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7009 70.09%
OATP2B1 inhibitior - 0.8406 84.06%
OATP1B1 inhibitior + 0.9230 92.30%
OATP1B3 inhibitior + 0.9313 93.13%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9453 94.53%
P-glycoprotein inhibitior - 0.9302 93.02%
P-glycoprotein substrate - 0.7606 76.06%
CYP3A4 substrate + 0.5203 52.03%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7431 74.31%
CYP3A4 inhibition - 0.9048 90.48%
CYP2C9 inhibition - 0.7194 71.94%
CYP2C19 inhibition - 0.6708 67.08%
CYP2D6 inhibition - 0.9357 93.57%
CYP1A2 inhibition - 0.7339 73.39%
CYP2C8 inhibition - 0.9385 93.85%
CYP inhibitory promiscuity - 0.7940 79.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion - 0.8547 85.47%
Eye irritation + 0.9684 96.84%
Skin irritation + 0.5845 58.45%
Skin corrosion - 0.9814 98.14%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4162 41.62%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.8626 86.26%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6193 61.93%
Acute Oral Toxicity (c) III 0.8226 82.26%
Estrogen receptor binding - 0.8180 81.80%
Androgen receptor binding + 0.5253 52.53%
Thyroid receptor binding - 0.7587 75.87%
Glucocorticoid receptor binding - 0.7730 77.30%
Aromatase binding - 0.7057 70.57%
PPAR gamma - 0.7270 72.70%
Honey bee toxicity - 0.8165 81.65%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6200 62.00%
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 92.83% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.58% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.83% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.28% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.65% 86.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.05% 95.89%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.05% 85.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.81% 100.00%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 81.06% 88.81%

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.
Lophozia ventricosa

Cross-Links

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PubChem 21586136
LOTUS LTS0213522
wikiData Q104967659