2-(1,3-Benzodioxol-5-ylmethyl)-1,3-dioxoisoindoline-5-carboxylic acid - CAS 214758-41-5
Category:
Main Product
Product Name:
2-(1,3-Benzodioxol-5-ylmethyl)-1,3-dioxoisoindoline-5-carboxylic acid
Catalog Number:
214758-41-5
Synonyms:
2-(1,3-Benzodioxol-5-ylmethyl)-1,3-dioxoisoindoline-5-carboxylic acid; 2-(1,3-Benzodioxol-5-yloxy)nicotinic acid
CAS Number:
214758-41-5
Molecular Weight:
259.21
Molecular Formula:
C13H9NO5
COA:
Inquire
MSDS:
Inquire
Canonical SMILES:
C1OC2=C(O1)C=C(C=C2)OC3=C(C=CC=N3)C(=O)O
InChI:
InChI=1S/C13H9NO5/c15-13(16)9-2-1-5-14-12(9)19-8-3-4-10-11(6-8)18-7-17-10/h1-6H,7H2,(H,15,16)
InChIKey:
HXXHQOGRXQVZCN-UHFFFAOYSA-N
Chemical Structure
CAS 214758-41-5 2-(1,3-Benzodioxol-5-ylmethyl)-1,3-dioxoisoindoline-5-carboxylic acid

Reference Reading


1.Physiological and biochemical effects of botanical extract from Piper nigrum Linn (Piperaceae) against the dengue vector Aedes aegypti Liston (Diptera: Culicidae).
Lija-Escaline J1, Senthil-Nathan S2, Thanigaivel A1, Pradeepa V1, Vasantha-Srinivasan P1, Ponsankar A1, Edwin ES1, Selin-Rani S1, Abdel-Megeed A3,4. Parasitol Res. 2015 Nov;114(11):4239-49. doi: 10.1007/s00436-015-4662-1. Epub 2015 Aug 16.
The leaves of Piper nigrum L. (Piperaceae) were evaluated for chemical constituents and mosquito larvicidal activity against the larvae of Aedes aegypti. GC and GC-MS analyses revealed that the crude extracts contain 16 compounds. Thymol (20.77%) and ç-elemene (10.42%) were identified as the major constituents followed by cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1 methylethyl)-, (3R-trans) (7.58%), 4,6-octadienoic acid, 2-acetyl-2-methyl-, ethyl ester (6.98), 2(3H)-furanone, 3,4-bis(1,3-benzodioxol-5-ylmethyl) dihydro-, (3R-trans) (6.95%), 1-naphthalenol, 1,2,3,4,4a,7,8,8a-octahydro-1,6-dimethyl-4-(1-methylethyl)-, [1R-(1à,4á,4aá,8aá)]-(Cedreanol) (5.30%), trans-2-undecen-1-ol (4.48%), phytol (4.22%), 1,6-cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-,[s-(E,E)] (3.78%) and 2,6-dimethyl-3,5,7-octatriene-2-ol, Z,Z (2.39%). Larval mortality was observed after 3 h of exposure period. The crude extract showed remarkable larvicidal activity against Ae.
2.The effect of phytocannabinoids on airway hyper-responsiveness, airway inflammation, and cough.
Makwana R1, Venkatasamy R2, Spina D2, Page C2. J Pharmacol Exp Ther. 2015 Apr;353(1):169-80. doi: 10.1124/jpet.114.221283. Epub 2015 Feb 5.
Cannabis has been demonstrated to have bronchodilator, anti-inflammatory, and antitussive activity in the airways, but information on the active cannabinoids, their receptors, and the mechanisms for these effects is limited. We compared the effects of Δ(9)-tetrahydrocannabinol, cannabidiol, cannabigerol, cannabichromene, cannabidiolic acid, and tetrahydrocannabivarin on contractions of the guinea pig-isolated trachea and bronchoconstriction induced by nerve stimulation or methacholine in anesthetized guinea pigs following exposure to saline or the proinflammatory cytokine, tumor necrosis factor α (TNF-α). CP55940 (2-[(1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl) cyclohexyl]-5-(2-methyloctan-2-yl)phenol), a synthetic cannabinoid agonist, was also investigated in vitro. The cannabinoids were also evaluated on TNF-α- and lipopolysaccharide-induced leukocyte infiltration into the lungs and citric acid-induced cough responses in guinea pigs. TNF-α, but not saline, augmented tracheal contractility and bronchoconstriction induced by nerve stimulation, but not methacholine.