Synonym
COH-SR4; COHSR4; COH SR4
IUPAC/Chemical Name
1,3-bis(3,5-dichlorophenyl)urea
InChi Key
VKVJIWVUYNTBEZ-UHFFFAOYSA-N
InChi Code
InChI=1S/C13H8Cl4N2O/c14-7-1-8(15)4-11(3-7)18-13(20)19-12-5-9(16)2-10(17)6-12/h1-6H,(H2,18,19,20)
SMILES Code
O=C(NC1=CC(Cl)=CC(Cl)=C1)NC2=CC(Cl)=CC(Cl)=C2
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
Preparing Stock Solutions
The following data is based on the
product
molecular weight
350.02
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1: Figarola JL, Rahbar S. Small‑molecule COH-SR4 inhibits adipocyte
differentiation via AMPK activation. Int J Mol Med. 2013 May;31(5):1166-76. doi:
10.3892/ijmm.2013.1313. Epub 2013 Mar 21. PMID: 23525347.
2: Figarola JL, Singhal P, Rahbar S, Gugiu BG, Awasthi S, Singhal SS. COH-SR4
reduces body weight, improves glycemic control and prevents hepatic steatosis in
high fat diet-induced obese mice. PLoS One. 2013 Dec 20;8(12):e83801. doi:
10.1371/journal.pone.0083801. PMID: 24376752; PMCID: PMC3869817.
3: Singhal SS, Figarola J, Singhal J, Leake K, Nagaprashantha L, Lincoln C,
Gabriel Gugiu B, Horne D, Jove R, Awasthi S, Rahbar S.
1,3-Bis(3,5-dichlorophenyl) urea compound 'COH-SR4' inhibits proliferation and
activates apoptosis in melanoma. Biochem Pharmacol. 2012 Dec 1;84(11):1419-27.
doi: 10.1016/j.bcp.2012.08.020. Epub 2012 Aug 28. PMID: 22959823; PMCID:
PMC3747778.
4: Singhal SS, Figarola J, Singhal J, Nagaprashantha L, Berz D, Rahbar S,
Awasthi S. Novel compound 1,3-bis (3,5-dichlorophenyl) urea inhibits lung cancer
progression. Biochem Pharmacol. 2013 Dec 15;86(12):1664-72. doi:
10.1016/j.bcp.2013.09.022. Epub 2013 Oct 4. PMID: 24099794; PMCID: PMC4186798.
5: Limbach KE, Wen W, Xing Q, Yan J, Yim JH. Baicalein activates 5' adenosine
monophosphate-activated protein kinase, inhibits the mammalian target of
rapamycin, and exhibits antiproliferative effects in pancreatic neuroendocrine
tumors in vitro and in vivo. Surgery. 2023 Jan;173(1):12-18. doi:
10.1016/j.surg.2022.07.030. Epub 2022 Oct 4. PMID: 36207198.