Casbene

Details

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Internal ID ba58c842-ad80-445d-a767-1f69095d2312
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (2E,6E,10E)-3,7,11,15,15-pentamethylbicyclo[12.1.0]pentadeca-2,6,10-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32/c1-15-8-6-10-16(2)12-13-18-19(20(18,4)5)14-17(3)11-7-9-15/h9-10,14,18-19H,6-8,11-13H2,1-5H3/b15-9+,16-10+,17-14+
InChI Key ZJMVJDFTNPZVMB-QOCMWZQCSA-N
Popularity 4 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 5.40
Atomic LogP (AlogP) 6.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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24286-51-9
(2E,6E,10E)-3,7,11,15,15-pentamethylbicyclo[12.1.0]pentadeca-2,6,10-triene
C01414
CHEBI:17695
LMPR0104290001
Q27102539

2D Structure

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2D Structure of Casbene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.9210 92.10%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6555 65.55%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9667 96.67%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5697 56.97%
P-glycoprotein inhibitior - 0.5275 52.75%
P-glycoprotein substrate - 0.9468 94.68%
CYP3A4 substrate + 0.5121 51.21%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8991 89.91%
CYP2C9 inhibition - 0.6993 69.93%
CYP2C19 inhibition - 0.6402 64.02%
CYP2D6 inhibition - 0.9299 92.99%
CYP1A2 inhibition - 0.6910 69.10%
CYP2C8 inhibition - 0.7429 74.29%
CYP inhibitory promiscuity - 0.7842 78.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.4661 46.61%
Eye corrosion - 0.8501 85.01%
Eye irritation - 0.8705 87.05%
Skin irritation + 0.6803 68.03%
Skin corrosion - 0.9651 96.51%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7940 79.40%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8733 87.33%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4685 46.85%
Acute Oral Toxicity (c) III 0.7166 71.66%
Estrogen receptor binding + 0.6347 63.47%
Androgen receptor binding - 0.6529 65.29%
Thyroid receptor binding + 0.6013 60.13%
Glucocorticoid receptor binding + 0.6177 61.77%
Aromatase binding - 0.6258 62.58%
PPAR gamma + 0.5209 52.09%
Honey bee toxicity - 0.8746 87.46%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.23% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.09% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.21% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.51% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.65% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.17% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.13% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 82.87% 97.79%
CHEMBL1871 P10275 Androgen Receptor 82.03% 96.43%
CHEMBL221 P23219 Cyclooxygenase-1 81.90% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.91% 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.
Ricinus communis

Cross-Links

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PubChem 5280437
LOTUS LTS0123910
wikiData Q27102539