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Home CSSS00015190582

Structure Info

Chemspace ID
CSSS00015190582 (In-Stock Screening Compounds)
MFCD
MFCD04343337
IUPAC Name
5-chloro-2-(4-methylpiperazine-1-carbonyl)-1H-indole
Mol formula
C14H16ClN3O
Mol weight
278 Da
Catalog Number(s)
20502, 111877, 142508, 10011925, 2490AH, 459168-41-3, A568763, AA0037Q5, AB49881, ACS-593, ADB4027276001, AG-10151, AG0037SX, AJ49881, AOS0037SX, AP459168413, AR0038HX, B1574, BBV-161722565, BD417964, BN0781, C75235, C75235-0.25G, CD31001857, CSC015190582, CSCR00035366718, D372544, ES-0048, HY-13508, IBS-E0824654, J211353, JH304137, JTA16841, LAN-B03428, LN00333730, LQT-B03448, M18565, OSSK_571319, PBMR221826, PV-002099427843, R699489, S2905, S86592, SAB-052436, STK175446, STOCK5S-76281, T2232, Z300149056, Z601-7640, a1_914_13525, s_527_153919_467458, s_527____153919____467458, scs-593

Properties

LogP
1.74
Heavy atoms count
19
Rotatable bond count
1
Number of rings
3
Carbon bond saturation, Fsp3
0.357
Polar surface area (Å)
39
Hydrogen bond acceptors count
2
Hydrogen bond donors count
1

SDS

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C14H16ClN3O
Zoom the structure
CSSS00015190582
 

Items Overall 33 items from 6 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
Key Organics Limited (BIONET)10 daysUnited Kingdom
To:
971 mg53
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Key Organics Limited (BIONET)10 daysUnited Kingdom
To:
975 mg62
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Key Organics Limited (BIONET)10 daysUnited Kingdom
To:
9710 mg75
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MedChemExpress10 daysUnited States
To:
995 mg80
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MedChemExpress10 daysUnited States
To:
9910 mg120
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MedChemExpress10 daysUnited States
To:
9950 mg350
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MedChemExpress10 daysUnited States
To:
99100 mg560
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MedChemExpress10 daysUnited States
To:
9910mM/1mL95
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Description: Names: JNJ-7777120; Product Description: JNJ-7777120 is a potent and selective histamine H 4 receptor antagonist ( K i =4.5 nM). JNJ-7777120 effectively blocks histamine-induced migration of mouse tracheal mast cells from connective tissue to epithelial cells. JNJ-7777120 also significantly blocks neutrophil infiltration in a mouse Zymosan-induced peritonitis model. JNJ-7777120 has a good potential to study antipruritic and anti-inflammatory .; Target: Histamine Receptor; CAS: 459168-41-3
MedChemExpress EU10 daysSweden
To:
995 mg85
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MedChemExpress EU10 daysSweden
To:
9910 mg126
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MedChemExpress EU10 daysSweden
To:
9950 mg369
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MedChemExpress EU10 daysSweden
To:
99100 mg590
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MedChemExpress EU10 daysSweden
To:
9910mM/1mL100
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Description: Names: JNJ-7777120; Product Description: JNJ-7777120 is a potent and selective histamine H4 receptor antagonist (Ki=4.5 nM). JNJ-7777120 effectively blocks histamine-induced migration of mouse tracheal mast cells from connective tissue to epithelial cells. JNJ-7777120 also significantly blocks neutrophil infiltration in a mouse Zymosan-induced peritonitis model. JNJ-7777120 has a good potential to study antipruritic and anti-inflammatory; Target: Histamine Receptor; CAS: 459168-41-3
Princeton Biomolecular Research10 daysUnited States
To:
901 mg88
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Princeton Biomolecular Research10 daysUnited States
To:
902 mg94
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Princeton Biomolecular Research10 daysUnited States
To:
905 mg99
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Princeton Biomolecular Research10 daysUnited States
To:
9010 mg116
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Princeton Biomolecular Research10 daysUnited States
To:
9015 mg132
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Princeton Biomolecular Research10 daysUnited States
To:
9020 mg143
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Princeton Biomolecular Research10 daysUnited States
To:
9050 mg231
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Princeton Biomolecular Research10 daysUnited States
To:
90100 mg297
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Princeton Biomolecular Research10 daysUnited States
To:
903 umol94
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Princeton Biomolecular Research10 daysUnited States
To:
905 umol99
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Apexbio Technology LLC10 daysUnited States
To:
985 mg101
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Apexbio Technology LLC10 daysUnited States
To:
9810 mg170
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Apexbio Technology LLC10 daysUnited States
To:
9850 mg466
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Apexbio Technology LLC10 daysUnited States
To:
98100 mg777
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Description: Name: JNJ-7777120; Histamine H4 receptor antagonist; Format: a crystalline solid; CAS: 459168-41-3
Targetmol Chemicals Inc30 daysUnited States
To:
995 mg64
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Targetmol Chemicals Inc30 daysUnited States
To:
9910 mg97
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Targetmol Chemicals Inc30 daysUnited States
To:
9925 mg173
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Targetmol Chemicals Inc30 daysUnited States
To:
9950 mg288
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Targetmol Chemicals Inc30 daysUnited States
To:
99100 mg463
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Targetmol Chemicals Inc30 daysUnited States
To:
99500 mg987
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Description: JNJ-7777120 is the first potent and selective non-imidazole histamine H4 receptor antagonist with Ki of 4.5 nM, exhibits >1000-fold selectivity over the other histamin receptors.; CAS: 459168-41-3
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