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NidufexorNidufexor (LMB763) is an orally available farnesoid X receptor (FXR) agonist for the research of nonalcoholic steatohepatitis (NASH). Product information CAS Number: 1773489 72 7 Molecular Weight: 487. 93 Formula: C27H22ClN3O4 Chemical Name: 4 [(N benzyl 1 {8 chloro 1 methyl 1H,4H chromeno[4,3 c]pyrazol 3 yl}formamido)methyl]benzoic acid Smiles: CN1N=C(C(=O)N(CC2C=CC(=CC=2)C(O)=O)CC2C=CC=CC=2)C2COC3=CC=C(Cl)C=C3C1=2 InChiKey: JYTIXGYXBIBOMN UHFFFAOYSA
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Nidufexor (LMB763) is an orally-available farnesoid X receptor (FXR) agonist for the research of nonalcoholic steatohepatitis (NASH).

Product information

CAS Number: 1773489-72-7

Molecular Weight: 487.93

Formula: C27H22ClN3O4

Chemical Name: 4-[(N-benzyl-1-{8-chloro-1-methyl-1H,4H-chromeno[4,3-c]pyrazol-3-yl}formamido)methyl]benzoic acid

Smiles: CN1N=C(C(=O)N(CC2C=CC(=CC=2)C(O)=O)CC2C=CC=CC=2)C2COC3=CC=C(Cl)C=C3C1=2

InChiKey: JYTIXGYXBIBOMN-UHFFFAOYSA-N

InChi: InChI=1S/C27H22ClN3O4/c1-30-25-21-13-20(28)11-12-23(21)35-16-22(25)24(29-30)26(32)31(14-17-5-3-2-4-6-17)15-18-7-9-19(10-8-18)27(33)34/h2-13H,14-16H2,1H3,(H,33,34)

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: DMSO : 83.33 mg/mL (170.78 mM; Need ultrasonic).

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vivo:

Nidufexor (LMB763) is a potent and specific FXR-gene modulator in vivo, reducing steatosis, inflammation and fibrosis in nonalcoholic steatohepatitis (NASH) murine models. Nidufexor exhibits moderate Cmax (4.5, 12.4, 28.1, 80.9, and 140.8 μM) and terminal elimination half-lives (t1/2; 3.9 5.7 6.3 5.6 6.3 h) following oral administration (3 ,10 ,30, 100, and 300mg/kg) in adult male Wistar Han rats (age approximately 10 weeks) Nidufexor exhibits terminal elimination half-lives (mouse 4.5, rat 4.4 and, dog 6.8 h) following intravenous administration (mouse 3.0, rat 5.0 and, dog 0.5 mg/kg). Nidufexor exhibits terminal elimination half-lives (mouse 3.5, rat 2.7 and, dog 10.1 h) following oral administration (mouse 10, rat 10 and, dog 2 mg/kg).

Products are for research use only. Not for human use.

Nidufexor

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