Inhibitory effect of cannabichromene, a major non-psychotropic cannabinoid extracted from Cannabis sativa, on inflammation-induced hypermotility in micePharmacological evaluation of the natural constituent of Cannabis sativa, cannabichromene and its modulation by Δ(9)-tetrahydrocannabinol.Biological activity of cannabichromene, its homologs and isomers.The effect of cannabichromene on adult neural stem/progenitor cells.Disposition of cannabichromene, cannabidiol, and Δ⁹-tetrahydrocannabinol and its metabolites in mouse brain following marijuana inhalation determined by high-performance liquid chromatography-tandem mass spectrometry.The cannabinoid TRPA1 agonist cannabichromene inhibits nitric oxide production in macrophages and ameliorates murine colitisStereospecific cyclizations and isomerizations of cannabichromene and related cannabinoids.Hashish components. Photochemical production of cannabicyclol from cannabichromene.In vitro metabolism of cannabichromene in seven common laboratory animals.Neurobehavioral actions of cannabichromene and interactions with delta 9-tetrahydrocannabinol.Cannabichromene and tetrahydrocannabinol determination in mouse blood and brain by gas chromatography-mass spectrometry.Intraocular pressure, ocular toxicity and neurotoxicity after administration of delta 9-tetrahydrocannabinol or cannabichromene.The effect of cannabichromene on mean blood pressure, heart rate, and respiration rate responses to tetrahydrocannabinol in the anesthetized rat.Constituents of Cannabis sativa L. 3. Clear and discrete separation of cannabidiol and cannabichromene.Constituents of Cannabis sativa L. XI: Cannabidiol and cannabichromene in samples of known geographical origin.Anti-inflammatory properties of cannabichromene.Biological Activity of Cannabichromene, its Homologs and IsomersDistinction of Synthetic Cannabidiol, Cannabichromene, and Cannabivarin by GLC Using On-Column Methylation
P921
Q28258759-a1eb8c11-04af-4e69-b969-175cc9ebee47Q34125281-fc11aa81-dbaa-437d-ac1e-2d3f9778a894Q34284008-9cf1f242-4fd6-4446-b0aa-2d464baa7e9bQ34363772-702744d5-b56c-4a97-ae30-6ef3f56d8057Q34505221-aaf9c26b-69a5-4c23-9e9c-1dc2dcfc8db4Q36784020-1a75d574-bc4f-4d8c-a740-5c5a83903b15Q43520447-ebeedbc0-4000-4be7-857f-23562a970996Q44051379-fbc0d22d-1385-4b5e-9a35-072b72ff1ca2Q46488487-85d74440-7b80-4bf0-89b0-05ad3ca961eeQ48847006-b9c380cc-ade0-4680-98a0-0fe01b432680Q48931740-ec1efcfa-42f0-46f7-bc04-b29314bfa655Q49095307-f28819e7-30c6-4e55-a229-4c5325427662Q52702256-9f477206-b554-4e34-9718-3d1edf757b3cQ53716881-0be63ca7-586d-414f-87b8-52c11ecdda68Q53998226-220c1c52-4d84-4e53-a7b8-67b10fbebed7Q55063149-a3537fb1-4f30-417b-a661-a1e9e352e220Q56429162-0a95e6db-84f9-44c8-8130-41a82feb7a14Q56482923-ba89f682-9730-4330-b7ee-9dbde91b49f0
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Cannabichromen
@de
Cannabichromene
@nl
Kanabichromen
@cs
Kanabihromen
@sh
Kanabihromen
@sr
Kannabichromen
@pl
canabicromeno
@pt
cannabichromene
@en
cannabicromene
@it
کانابیچرومن
@azb
type
label
Cannabichromen
@de
Cannabichromene
@nl
Kanabichromen
@cs
Kanabihromen
@sh
Kanabihromen
@sr
Kannabichromen
@pl
canabicromeno
@pt
cannabichromene
@en
cannabicromene
@it
کانابیچرومن
@azb
altLabel
Cannabichromene
@pt
prefLabel
Cannabichromen
@de
Cannabichromene
@nl
Kanabichromen
@cs
Kanabihromen
@sh
Kanabihromen
@sr
Kannabichromen
@pl
canabicromeno
@pt
cannabichromene
@en
cannabicromene
@it
کانابیچرومن
@azb
P592
P6366
P646
P661
P662
P665
P683
P2064
P2067
P231
20675-51-8
P232
P233
CCCCCC1=CC2=C(C=CC(O2)(C)CCC=C(C)C)C(=C1)O
P234
1S/C21H30O2/c1-5-6-7-10-17-14- ...... 11,13-15,22H,5-8,10,12H2,1-4H3
P235
UVOLYTDXHDXWJU-UHFFFAOYSA-N
P2566
100.236.929
P274
P3117
DTXSID80942873
P592
CHEMBL422704
P6366
2778825661
P646
/m/04jc76c
P652
K4497H250W