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Home CSCS00025766756

Structure Info

Chemspace ID
CSCS00025766756 (Synthesis)
MFCD
MFCD00864800
IUPAC Name
ethyl {[2-chloro-5-cyano-3-(2-ethoxy-2-oxoacetamido)phenyl]carbamoyl}formate
Mol formula
C15H14ClN3O6
Mol weight
368 Da
Catalog Number(s)
53882-13-6, AA00E3QE, ACM53882136, AD248594, AG00E3T6, AG57922, APB53882136, AR00E4I6, CSC025766756, HY-167706, JH331073, T68094, Y3305437, ZXC320646

Properties

LogP
2.3
Heavy atoms count
25
Rotatable bond count
8
Number of rings
1
Carbon bond saturation, Fsp3
0.266
Polar surface area (Å)
135
Hydrogen bond acceptors count
5
Hydrogen bond donors count
2

SDS

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C15H14ClN3O6
Zoom the structure
CSCS00025766756
 

Items Overall 26 items from 9 suppliers

SupplierLead timeShips fromPurityPackPrice, €Qty
Angene US10 daysUnited States
To:
951 mg91
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Description: Lodoxamide ethyl; CAS: 53882-13-6
MedChemExpress30 daysUnited States
To:
901 mg162
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MedChemExpress30 daysUnited States
To:
905 mg385
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MedChemExpress30 daysUnited States
To:
9010 mg575
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MedChemExpress30 daysUnited States
To:
9025 mg976
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MedChemExpress30 daysUnited States
To:
9050 mg1,408
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Description: Names: Diethyl-Lodoxamide; Product Description: Diethyl-Lodoxamide is a highly potent GPR35 agonist with potential to inhibit inflammatory bowel disease. Diethyl-Lodoxamide activates GPR35 in humans, mice and rats, showing similar EC 50 values. Diethyl-Lodoxamide can alleviate the clinical symptoms of DSS-induced inflammatory bowel disease in mouse models, and the effect is better than the traditional drug 5-ASA. The pharmaceutical properties of Diethyl-Lodoxamide have been optimized to better meet the requirements of drug design .; Target: GPR35; CAS: 53882-13-6
MedChemExpress EU30 daysSweden
To:
901 mg170
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MedChemExpress EU30 daysSweden
To:
905 mg406
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MedChemExpress EU30 daysSweden
To:
9010 mg605
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MedChemExpress EU30 daysSweden
To:
9025 mg1,029
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MedChemExpress EU30 daysSweden
To:
9050 mg1,483
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Description: Names: Diethyl-Lodoxamide; Product Description: Diethyl-Lodoxamide is a highly potent GPR35 agonist with potential to inhibit inflammatory bowel disease. Diethyl-Lodoxamide activates GPR35 in humans, mice and rats, showing similar EC50 values. Diethyl-Lodoxamide can alleviate the clinical symptoms of DSS-induced inflammatory bowel disease in mouse models, and the effect is better than the traditional drug 5-ASA. The pharmaceutical properties of Diethyl-Lodoxamide have been optimized to better meet the requirements of drug design; Target: GPR35; CAS: 53882-13-6
Advanced ChemBlock Inc30 daysUnited States
To:
985 mg264
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Advanced ChemBlock Inc30 daysUnited States
To:
9810 mg391
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Advanced ChemBlock Inc30 daysUnited States
To:
9825 mg737
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Advanced ChemBlock Inc30 daysUnited States
To:
98100 mg1,375
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Advanced ChemBlock Inc30 daysUnited States
To:
98250 mg2,750
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Description: Lodoxamide ethyl; CAS: 53882-13-6
AA BLOCKS35 daysUnited States
To:
951 mg132
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AA BLOCKS35 daysUnited States
To:
955 mg255
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AA BLOCKS35 daysUnited States
To:
9510 mg352
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AA BLOCKS35 daysUnited States
To:
9525 mg623
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AA BLOCKS35 daysUnited States
To:
9550 mg812
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AA BLOCKS35 daysUnited States
To:
95100 mg1,115
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Description: lodoxamide ethyl; CAS: 53882-13-6
Alfa ChemistryTBDUnited States
To:
951 gPOA
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Description: CAS: 53882-13-6
Alfa Chemistry Analytical ProductsTBDUnited States
To:
951 gPOA
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BOC SciencesTBDUnited States
To:
951 gPOA
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Description: CAS: 53882-13-6
Zerenex Molecular LtdTBDUnited Kingdom
To:
951 gPOA
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Description: CAS: 53882-13-6
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