JNJ-7777120

Suppliers

Names

[ CAS No. ]:
459168-41-3

[ Name ]:
JNJ-7777120

[Synonym ]:
Methanone, (5-chloro-1H-indol-2-yl)(4-methyl-1-piperazinyl)-
(5-Chloro-1H-indol-2-yl)(4-methyl-1-piperazinyl)methanone
JNJ-7777120
(5-chloro-1H-indol-2-yl)(4-methylpiperazin-1-yl)methanone
(5-chloro-1H-indol-2-yl)-(4-methylpiperazin-1-yl)methanone
1-((5-chloro-1H-indol-2-yl)carbonyl)-4-methylpiperazine

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
477.0±45.0 °C at 760 mmHg

[ Molecular Formula ]:
C14H16ClN3O

[ Molecular Weight ]:
277.749

[ Flash Point ]:
242.3±28.7 °C

[ Exact Mass ]:
277.098175

[ PSA ]:
39.34000

[ LogP ]:
0.69

[ Appearance of Characters ]:
solid | white

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.656

[ Storage condition ]:
Store at +4°C

[ Water Solubility ]:
H2O: insoluble

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Precursor & DownStream

Precursor

  • methylpiperazine
  • 5-Chloroindole-2-carboxylic acid

DownStream

Articles

Involvement of the H1 Histamine Receptor, p38 MAP Kinase, Myosin Light Chains Kinase, and Rho/ROCK in Histamine-Induced Endothelial Barrier Dysfunction.

Microcirculation 22 , 237-48, (2015)

The mechanisms by which histamine increases microvascular permeability remain poorly understood. We tested the hypothesis that H1 receptor activation disrupts the endothelial barrier and investigated ...

Histamine H4 receptor as a new therapeutic target for choroidal neovascularization in age-related macular degeneration.

Br. J. Pharmacol. 171(15) , 3754-63, (2014)

The present treatment for choroidal neovascularization (CNV) associated with age-related macular degeneration (AMD) is not sufficient. Hence, we examined the therapeutic efficacy of reducing histamine...

Analysis of the histamine H2-receptor in human monocytes.

Biochem. Pharmacol. 92(2) , 369-79, (2014)

Histamine receptors are G-protein-coupled receptors (GPCRs). Canonically, the histamine H2-receptor (H2R) couples to Gs-proteins and activates adenylyl cyclases (ACs) with subsequent adenosine-3',5'-c...


More Articles


Related Compounds

  • JNJ 41876666
  • JNJ 10397049
  • JNJ-38893777 sulfate
  • JNJ-61803534
  • JNJ-7706621
  • JNJ-42253432
  • (4-((1H-imidazol-1-yl)methyl)phenyl)(3-(4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl)azetidin-1-yl)methanone
  • 5-(3-iodo-1H-pyrazol-1-yl)-3-methoxypyridazine
  • 2-Ethynyl-5-thiazolepropanoic acid methyl ester
  • 3-((1H-pyrazol-1-yl)methyl)-5,6,7,8-tetrahydro-4H-[1,2,3]triazolo[1,5-a][1,4]diazepine
  • 2-(4-fluorobenzoyl)-N-{[2-(furan-2-yl)pyridin-3-yl]methyl}benzamide
  • N-Methyl-N-((6,7,8,9-Tetrahydro-5H-[1,2,4]Triazolo[4,3-A][1,4]Diazepin-3-Yl)Methyl)Propan-2-Amine
  • 3-(piperidin-1-ylmethyl)-6,7,8,9-tetrahydro-5H-[1,2,4]triazolo[4,3-a][1,4]diazepine
  • N-((4,5,6,7-Tetrahydroisoxazolo[4,5-c]pyridin-3-yl)methyl)pyrimidin-2-amine
  • N-(2-Cyanophenyl)-N-ethylmethanesulfonamide
  • N-Butyl-N-(2-cyanophenyl)methanesulfonamide
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