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CRT0273750 - 98%, high purity , CAS No.1979939-16-6

  • ≥98%
Item Number
C647993
Grouped product items
SKUSizeAvailabilityPrice Qty
C647993-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$71.90
C647993-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$150.90
C647993-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$240.90
C647993-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$540.90
C647993-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$920.90
C647993-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,600.90
View related series
GPCR/G Protein LPL Receptor

Basic Description

Specifications & Purity98%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

CRT0273750 is an autotaxin (ATX) inhibitor and modulates LPA levels in plasm (IC 50 = 0.014 μM). CRT0273750 can be used in ATX/LPA-dependent models of cancer

In Vitro

CRT0273750 shows high potency in both the biochemical (IC 50 = 0.01 μM) and plasma choline release assay(IC 50 = 0.014 μM). CRT0273750 is also shown to inhibit the migration of 4T1 cells with an EC50 of 0.025μM. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

CRT0273750 (1 mg/kg; i.v.)has a moderate blood clearance, with value of 41 mL/min/kg . CRT0273750 (10 mg/kg; oral administration) treatment shows the C max , AUC and t 1/2 values of 3.8 µM, 3.2 µM.h and 1.4 h, respectively . CRT0273750 (10, 30 and 100 mg/kg; oral administration) shows a proportional increase . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: CD-1 mice Dosage: 1 mg/kg Administration: I.v. Result: Had a moderate blood clearance. Animal Model: Balb-c nu/nu mice Dosage: 10, 30 and 100 mg/kg Administration: Oral administration (Pharmacokinetic Analysis) Result: The C max s were 3.8, 10.9 and 18.1 µM, respectively. The AUCs were 3.2, 15.2 and 59.3 µM.h, respectively. The t 1/2 s were 1.4, 0.9 and 1.3 h, respectively.

Form:Solid

IC50& Target:IC50: 0.014 μM (plasma CRA)

Associated Targets

ENPP2 Tchem Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 4 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name N-[(1S)-1-(4-chlorophenyl)ethyl]-3-[3-[[4-(trifluoromethoxy)phenyl]methyl]imidazo[4,5-b]pyridin-2-yl]propanamide
INCHI InChI=1S/C25H22ClF3N4O2/c1-16(18-6-8-19(26)9-7-18)31-23(34)13-12-22-32-21-3-2-14-30-24(21)33(22)15-17-4-10-20(11-5-17)35-25(27,28)29/h2-11,14,16H,12-13,15H2,1H3,(H,31,34)/t16-/m0/s1
InChi Key HXYXHSDYBDFOFO-INIZCTEOSA-N
Canonical SMILES CC(C1=CC=C(C=C1)Cl)NC(=O)CCC2=NC3=C(N2CC4=CC=C(C=C4)OC(F)(F)F)N=CC=C3
Isomeric SMILES C[C@@H](C1=CC=C(C=C1)Cl)NC(=O)CCC2=NC3=C(N2CC4=CC=C(C=C4)OC(F)(F)F)N=CC=C3
PubChem CID 122199235
Molecular Weight 502.92

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilityDMSO : 250 mg/mL (497.10 mM; Need ultrasonic)

Related Documents

Solution Calculators