MedKoo Cat#: 525221 | Name: TCS2312
Featured

Description:

WARNING: This product is for research use only, not for human or veterinary use.

TCS2312 is a novel potent and selective CHK1 kinase inhibitor. Inhibition of Chk1 with TCS2312 or knockdown of Chk1 profoundly attenuates CPX-induced Cdc25A degradation in the cells.

Chemical Structure

TCS2312
TCS2312
CAS#838823-31-7

Theoretical Analysis

MedKoo Cat#: 525221

Name: TCS2312

CAS#: 838823-31-7

Chemical Formula: C25H24N4O2

Exact Mass: 412.1899

Molecular Weight: 412.49

Elemental Analysis: C, 72.80; H, 5.86; N, 13.58; O, 7.76

Price and Availability

Size Price Availability Quantity
1mg USD 550.00 2 Weeks
Bulk Inquiry
Buy Now
Add to Cart
Related CAS #
No Data
Synonym
TCS2312, TCS 2312, TCS-2312;
IUPAC/Chemical Name
4'-[5-[[3-[(Cyclopropylamino)methyl]phenyl]amino]-1H-pyrazol-3-yl]-[1,1'-biphenyl]-2,4-diol
InChi Key
JMEXWOPTERDPHI-UHFFFAOYSA-N
InChi Code
InChI=1S/C25H24N4O2/c30-21-10-11-22(24(31)13-21)17-4-6-18(7-5-17)23-14-25(29-28-23)27-20-3-1-2-16(12-20)15-26-19-8-9-19/h1-7,10-14,19,26,30-31H,8-9,15H2,(H2,27,28,29)
SMILES Code
OC1=CC(O)=CC=C1C2=CC=C(C3=NNC(NC4=CC=CC(CNC5CC5)=C4)=C3)C=C2
Appearance
Solid powder
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
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
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
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 412.49 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.

Recalculate based on batch purity %
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: Sproul CD, Rao S, Ibrahim JG, Kaufmann WK, Cordeiro-Stone M. Is activation of the intra-S checkpoint in human fibroblasts an important factor in protection against UV-induced mutagenesis? Cell Cycle. 2013 Nov 15;12(22):3555-63. doi: 10.4161/cc.26590. Epub 2013 Sep 25. PubMed PMID: 24091629; PubMed Central PMCID: PMC3906341. 2: Cole KA, Huggins J, Laquaglia M, Hulderman CE, Russell MR, Bosse K, Diskin SJ, Attiyeh EF, Sennett R, Norris G, Laudenslager M, Wood AC, Mayes PA, Jagannathan J, Winter C, Mosse YP, Maris JM. RNAi screen of the protein kinome identifies checkpoint kinase 1 (CHK1) as a therapeutic target in neuroblastoma. Proc Natl Acad Sci U S A. 2011 Feb 22;108(8):3336-41. doi: 10.1073/pnas.1012351108. Epub 2011 Feb 2. PubMed PMID: 21289283; PubMed Central PMCID: PMC3044382. 3: Shen T, Zhou H, Shang C, Luo Y, Wu Y, Huang S. Ciclopirox activates ATR-Chk1 signaling pathway leading to Cdc25A protein degradation. Genes Cancer. 2018 Jan;9(1-2):39-52. doi: 10.18632/genesandcancer.166. PMID: 29725502; PMCID: PMC5931253.