HC-030031

HC-030031
Identifiers
	IUPAC name 2-(1,3-dimethyl-2,6-dioxopurin-7-yl)-N-(4-propan-2-ylphenyl)acetamide;
CAS Number	349085-38-7 ;
PubChem CID	1150897;
ChemSpider	976407;
UNII	MU78VFH9C7;
ChEMBL	ChEMBL1086310;
Chemical and physical data
Formula	C18H21N5O3
Molar mass	355.398 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC(C)C1=CC=C(C=C1)NC(=O)CN2C=NC3=C2C(=O)N(C(=O)N3C)C;
	InChI InChI=1S/C18H21N5O3/c1-11(2)12-5-7-13(8-6-12)20-14(24)9-23-10-19-16-15(23)17(25)22(4)18(26)21(16)3/h5-8,10-11H,9H2,1-4H3,(H,20,24); Key:HEQDZPHDVAOBLN-UHFFFAOYSA-N;

Short description: Chemical compound

HC-030031 is a drug which acts as a potent and selective antagonist for the TRPA1 receptor, and has analgesic and antiinflammatory effects.^[1]^[2]^[3]^[4]

References

↑ "HC-030031, a TRPA1 selective antagonist, attenuates inflammatory- and neuropathy-induced mechanical hypersensitivity". Molecular Pain 4: 1744-8069-4-48. October 2008. doi:10.1186/1744-8069-4-48. PMID 18954467.
↑ "Blockade of TRPA1 with HC-030031 attenuates visceral nociception by a mechanism independent of inflammatory resident cells, nitric oxide and the opioid system". European Journal of Pain 17 (2): 223–33. February 2013. doi:10.1002/j.1532-2149.2012.00177.x. PMID 22689151. http://www.repositorio.ufc.br/handle/riufc/7249.
↑ "TRPA1: a transducer and amplifier of pain and inflammation". Basic & Clinical Pharmacology & Toxicology 114 (1): 50–5. January 2014. doi:10.1111/bcpt.12138. PMID 24102997.
↑ "TRPA1 and CGRP antagonists counteract vesicant-induced skin injury and inflammation". Toxicology Letters 293: 140–148. September 2018. doi:10.1016/j.toxlet.2018.03.007. PMID 29535050.

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/HC-030031. Read more

[1] "HC-030031, a TRPA1 selective antagonist, attenuates inflammatory- and neuropathy-induced mechanical hypersensitivity". Molecular Pain 4: 1744-8069-4-48. October 2008. doi:10.1186/1744-8069-4-48. PMID 18954467.

[2] "Blockade of TRPA1 with HC-030031 attenuates visceral nociception by a mechanism independent of inflammatory resident cells, nitric oxide and the opioid system". European Journal of Pain 17 (2): 223–33. February 2013. doi:10.1002/j.1532-2149.2012.00177.x. PMID 22689151. http://www.repositorio.ufc.br/handle/riufc/7249.

[3] "TRPA1: a transducer and amplifier of pain and inflammation". Basic & Clinical Pharmacology & Toxicology 114 (1): 50–5. January 2014. doi:10.1111/bcpt.12138. PMID 24102997.

[4] "TRPA1 and CGRP antagonists counteract vesicant-induced skin injury and inflammation". Toxicology Letters 293: 140–148. September 2018. doi:10.1016/j.toxlet.2018.03.007. PMID 29535050.

[1]

[2]

[3]

[4]

Identifiers

IUPAC name 2-(1,3-dimethyl-2,6-dioxopurin-7-yl)-N-(4-propan-2-ylphenyl)acetamide
CAS Number	349085-38-7^Y
PubChem CID	1150897
ChemSpider	976407
UNII	MU78VFH9C7
ChEMBL	ChEMBL1086310
Chemical and physical data
Formula	C₁₈H₂₁N₅O₃
Molar mass	355.398 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES CC(C)C1=CC=C(C=C1)NC(=O)CN2C=NC3=C2C(=O)N(C(=O)N3C)C
InChI InChI=1S/C18H21N5O3/c1-11(2)12-5-7-13(8-6-12)20-14(24)9-23-10-19-16-15(23)17(25)22(4)18(26)21(16)3/h5-8,10-11H,9H2,1-4H3,(H,20,24) Key:HEQDZPHDVAOBLN-UHFFFAOYSA-N

HC-030031

Topic: Chemistry

References