Ki16425 CAS: 355025-24-0
MF: C23H23ClN2O5S
MW: 475.0
A competitive inhibitor of EDG-2, EDG-4, and EDG-7.

Ki16425 (CAS 355025-24-0)

Ki16425 | CAS 355025-24-0 is rated 5.0 out of 5 by 1.
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Alternate Names: 3-[[[4-[4-[[[1-(2-Chlorophenyl)ethoxy]carbonyl]amino]-3-methyl-5-isoxazolyl]phenyl]methyl]thio]propanoic acid
Application: Ki16425 is a competitive inhibitor of EDG-2, EDG-4, and EDG-7
CAS Number: 355025-24-0
Purity: ≥95%
Molecular Weight: 475.0
Molecular Formula: C23H23ClN2O5S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data (including water content).

Ki16425 is a competitive, potent, and reversible inhibitor of EDG-2 (Ki = 0.34 μM), EDG-4 (Ki = 6.5 μM), and EDG-7 (Ki = 0.93 μM).


References

1. Ohta, H., et al. 2003. Mol. Pharmacol. 64: 994-1005. PMID: 14500756
2. Yamada, T., et al. 2004. J. Biol. Chem. 279: 6595-6605. PMID: 14660630
3. Choi, J.W., et al. 2008. Biochim. Biophys. Acta. 1781: 531-539. PMID: 18407842

Appearance :
Powder
Physical State :
Solid
Solubility :
Soluble in ethanol (95 mg/ml at 25° C), DMSO (95 mg/ml at 25° C), DMF (~10 mg/ml), 1: 4 solution of DMSO: PBS (pH 7.2) (~0.2 mg/ml), and water (<1 mg/ml at 25° C).
Storage :
Store at -20° C
Melting Point :
59.5-60.5° C
Boiling Point :
623.7° C at 760 mmHg (Predicted)
Density :
1.35 g/cm3 (Predicted)
Refractive Index :
n20D 1.63 (Predicted)
IC50 :
EDG-2: IC50 = 46 nM (human); EDG-7: IC50 = 301 nM (human)
Ki Data :
EDG-7: Ki= 148 nM (human); EDG-2: Ki= 0.17 µM (THP-1 fibroblasts); EDG-2: Ki= 0.34 µM (human); EDG-4: Ki= 0.54 µM (3T3 fibroblasts); EDG-4: Ki= 6.5 µM (human)
pK Values :
pKa: 4.32 (Predicted)
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
WGK Germany :
3
PubChem CID :
MDL Number :
MFCD06798341
SMILES :
CC1=NOC(=C1NC(=O)OC(C)C2=CC=CC=C2Cl)C3=CC=C(C=C3)CSCCC(=O)O

Download SDS (MSDS)

Certificate of Analysis

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Ki16425 (CAS 355025-24-0)  Product Citations

See how others have used Ki16425 (CAS 355025-24-0). Click on the entry to view the PubMed entry .

Citations 1 to 10 of 15 total

PMID: # 30840161  Olianas, MC.|Dedoni, S.|Onali, P.| et al. 2019. Apoptosis.

PMID: # 31017922  Konno, T.|Kotani, T.|Setiawan, J.|Nishigaito, Y.|Sawada, N.|Imada, S.|Saito, Y.|Murata, Y.|Matozaki, T.| et al. 2019. PLoS ONE. 14: e0215255.

PMID: # 29856906  Zhang, R.|Wang, J.| et al. 2018. Cancer Sci. 109: 2446-2457.

PMID: # 30181697  Nam, JS.|Sharma, AR.|Nguyen, LT.|Jagga, S.|Lee, YH.|Sharma, G.|Lee, SS.| et al. 2018. Korean J. Physiol. Pharmacol. 22: 503-511.

PMID: # 27605627  Olianas, MC. et al. 2016. J. Pharmacol. Exp. Ther. 359: 340-353.

PMID: # 26740622  Kedziora, KM. et al. 2016. J. Biol. Chem. 291: 4323-33.

PMID: # 25959255  Ohashi, T. et al. 2015. Exp. Dermatol. 24: 698-702.

PMID: # 25888927  Olianas, M.C. et al. 2015. Biochemical pharmacology. 95: 311-23.

PMID: # 24928086  Brusevold, IJ. et al. 2014. BMC Cancer. 14: 432.

PMID: # 27500235  Transplant Direct. e35.

Citations 1 to 10 of 15 total

What is the appearance of the compound?

Asked by: two2igm05
Thank you for your question. The appearance of Ki16425, sc-221788, is an off-white powder.
Answered by: TechService7
Date published: 2017-01-03
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Rated 5 out of 5 by from Zhao Zhao, J. et al. (PubMed 25701366) found that the lysophosphatidic acid receptor 1 antagonist Ki16425 blunts abdominal and systemic inflammation in a mouse model of peritoneal sepsis. -SCBT Publication Review
Date published: 2015-05-01
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