GSK962
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    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H561561

CAS#: 2049872-86-6

Description: GSK962 is a negative control for GSK963, a highly potent and selective RIP1 inhibitor.


Chemical Structure

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GSK962
CAS# 2049872-86-6

Theoretical Analysis

Hodoodo Cat#: H561561
Name: GSK962
CAS#: 2049872-86-6
Chemical Formula: C14H18N2O
Exact Mass: 230.14
Molecular Weight: 230.311
Elemental Analysis: C, 73.01; H, 7.88; N, 12.16; O, 6.95

Price and Availability

Size Price Availability Quantity
5mg USD 285 2 Weeks
25mg USD 450 2 Weeks
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Synonym: GSK'962; GSK 962; GSK962; GSK-962

IUPAC/Chemical Name: 2,2-Dimethyl-1-(5(R)-phenyl-4,5-dihydro-pyrazol-1-yl)-propan-1-one

InChi Key: NJQVSLWJBLPTMD-GFCCVEGCSA-N

InChi Code: InChI=1S/C14H18N2O/c1-14(2,3)13(17)16-12(9-10-15-16)11-7-5-4-6-8-11/h4-8,10,12H,9H2,1-3H3/t12-/m1/s1

SMILES Code: CC(C)(C)C(N1N=CC[C@@H]1C2=CC=CC=C2)=O

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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 230.31 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Berger SB, Harris P, Nagilla R, Kasparcova V, Hoffman S, Swift B, Dare L, Schaeffer M, Capriotti C, Ouellette M, King BW, Wisnoski D, Cox J, Reilly M, Marquis RW, Bertin J, Gough PJ. Characterization of GSK'963: a structurally distinct, potent and selective inhibitor of RIP1 kinase. Cell Death Discov. 2015 Jul 27;1:15009. doi: 10.1038/cddiscovery.2015.9. eCollection 2015. PubMed PMID: 27551444; PubMed Central PMCID: PMC4979471.