IMPPAT Phytochemical information: 
beta-Caryophyllene

beta-Caryophyllene
Summary

SMILES: C/C/1=C\CCC(=C)[C@@H]2[C@@H](CC1)C(C2)(C)C
InChI: InChI=1S/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6+/t13-,14-/m1/s1
InChIKey: NPNUFJAVOOONJE-GFUGXAQUSA-N
DeepSMILES: C/C=C\CCC=C)[C@@H][C@@H]CC\9))CC4)C)C
Scaffold Graph/Node/Bond level: C=C1CCC=CCCC2CCC12
Scaffold Graph/Node level: CC1CCCCCCC2CCC12
Scaffold Graph level: CC1CCCCCCC2CCC12
Functional groups: C/C=C(\C)C; C=C(C)C
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Prenol lipids
ClassyFire Subclass: Sesquiterpenoids
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Sesquiterpenoids
NP Classifier Class: Caryophyllane sesquiterpenoids
Synonymous chemical names:
β caryophyllene, beta-caryophyllene*, (e)-caryophyllene, bcaryophyllene, β-caryop hyl lene, caryophylene, caryophyllene, beta, beta-caryophyllene, caryophyllene, β-caryophyl- lene, β-caryophyllene (+β-cedrene?), β- caryophyllene, β -caryophyllene, caryoph yllene, (−) (e)-caryophyllene, β--caryophyllene, (-)-β-caryophyllene, β-caryop hyllene, caryophyllene, beta-, β-caryophyllene, (e)-caryophyllene(β-caryophyllene), *β-caryophyllene, caryophyllene*, (e)-caryophyllene-2, trans-caryophyllene, β- caryophyllene 0.3 5.3, (-)-Caryophyllene, β- -caryophyllene, β-caryophyllenea, Caryophyllene, trans-caryophylene, (b)-caryophyllene, β- caryoph yllene, β-caryophyllene1, (e)-caryophellene
External chemical identifiers:
CID:CID_5281515; ChEMBL:CHEMBL445740; ChEBI:CHEBI:10357; ZINC:ZINC000008234282; FDASRS:BHW853AU9H; SureChEMBL:SCHEMBL113830; MolPort-001-793-250
Chemical structure download


beta-Caryophyllene
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 204.36
Log P RDKit 4.73
Topological polar surface area (Å2) RDKit 0
Number of hydrogen bond acceptors RDKit 0
Number of hydrogen bond donors RDKit 0
Number of carbon atoms RDKit 15
Number of heavy atoms RDKit 15
Number of heteroatoms RDKit 0
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 2
Stereochemical complexity RDKit 0.13
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 4
Number of sp3 hybridized carbon atoms RDKit 11
Shape complexity RDKit 0.73
Number of rotatable bonds RDKit 0
Number of aliphatic carbocycles RDKit 2
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 2
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 2
Number of saturated carbocycles RDKit 1
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 1
Number of Smallest Set of Smallest Rings (SSSR) RDKit 2


beta-Caryophyllene
Drug-likeness
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 0
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 0
Ghose filter RDKit Passed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.500562


beta-Caryophyllene
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -4.44
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 1
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME Yes
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME No


beta-Caryophyllene
Phytochemical - Human target proteins supported by experimental evidence associations
Human target proteins supported by experimental evidence
IMPPAT target identifierGene identifierHGNC symbolEntrez Gene identifierSource
TAR_EXP_000004ENSG00000094631HDAC610013ChEMBL
TAR_EXP_000061ENSG00000134538SLCO1B110599ChEMBL, NPASS
TAR_EXP_000188ENSG00000188822CNR21269BindingDB, ChEMBL, NPASS
TAR_EXP_000880ENSG00000118058KMT2A4297NPASS
TAR_EXP_001166ENSG00000186951PPARA5465ChEMBL
TAR_EXP_000616ENSG00000111700SLCO1B328234ChEMBL, NPASS