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ChemicalBook--->CAS DataBase List--->844639-57-2

844639-57-2

844639-57-2 Structure

844639-57-2 Structure
IdentificationBack Directory
[Name]

(+)-3-[[(4-FLUOROPHENYL)SULFONYL]METHYLAMINO]-1,2,3,4-TETRAHYDRO-9H-CARBAZOLE-9-ACETIC ACID
[CAS]

844639-57-2
[Synonyms]

TM30089
CS-1157
TM30089 Racemate
TM 30089;TM-30089
CAY10471 Racemate
TM30089 (CAY10471)
9H-Carbazole-9-acetic acid, 3-[[(4-fluorophenyl)sulfonyl]MethylaMino]-1,2,3,4-tetrahydro-
(+)-3-[[(4-FLUOROPHENYL)SULFONYL]METHYLAMINO]-1,2,3,4-TETRAHYDRO-9H-CARBAZOLE-9-ACETIC ACID
[Molecular Formula]

C21H21FN2O4S
[MDL Number]

MFCD08062186
[MOL File]

844639-57-2.mol
[Molecular Weight]

416.47
Chemical PropertiesBack Directory
[Melting point ]

165-173℃ (dichloromethane )
[Boiling point ]

639.1±65.0 °C(Predicted)
[density ]

1.41±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 150 mg/mL (360.17 mM)
[form ]

Solid
[pka]

4.33±0.10(Predicted)
[color ]

Off-white to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H315-H317-H319-H410
[Precautionary statements ]

P273-P280-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

CAY10471 Racemate (TM30089 Racemate) is a potent and highly selective prostaglandin D2 receptor CRTH2 antagonist, with a Ki of 0.6 nM for hCRTH2, selective over human thromboxane A2 receptor TP (Ki, >10000 nM) or PGD2 receptor DP (Ki, 1200 nM). CAY10471 Racemate also has effect on mouse and rat orthologs of CRTH2[1].
[Biological Activity]

TM30089 is a ramatroban analog and an orally activehigh-affinitypotent and selective prostaglandin D2 receptor 2 (DP2; CRTH2) antagonist (Ki = 0.6 nM/hDP2 against 1.2 nM PGD2; Ki = 1.2 μM/hDP1 against 0.5 nM PGD2>10 μM/hTP against 5 nM SQ29548) th at blocks PGD2-induced responses in hDP2 transfectants (IP1/βarr IC50 = 1.2/3.0 nM) and exhibits in vivo efficacy in a murine model of renal tubulointerstitial fibrosis (20 mg/kg b.i.d. p.o.starting 4 days before or 3 days after unilateral ureteral obstruction/UUO).
[IC 50]

CRTH2: 0.6 nM (Ki)
[storage]

Store at -20°C
[References]

[1] Ulven T, et al. Minor structural modifications convert the dual TP/CRTH2 antagonist ramatroban into a highly selective and potent CRTH2 antagonist. J Med Chem. 2005 Feb 24;48(4):897-900. DOI:10.1021/jm049036i
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