MedKoo Cat#: 555407 | Name: GSK2643943A
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Description:

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

GSK2643943A is a potent USP20 inhibitor with IC50 = 160 nM.

Chemical Structure

GSK2643943A
GSK2643943A
CAS#2449301-27-1 (free base)

Theoretical Analysis

MedKoo Cat#: 555407

Name: GSK2643943A

CAS#: 2449301-27-1 (free base)

Chemical Formula: C17H12FN3

Exact Mass: 277.1015

Molecular Weight: 277.30

Elemental Analysis: C, 73.63; H, 4.36; F, 6.85; N, 15.15

Price and Availability

Size Price Availability Quantity
5mg USD 90.00 Ready to ship
10mg USD 165.00 Ready to ship
25mg USD 350.00 Ready to ship
50mg USD 550.00 Ready to ship
100mg USD 950.00 Ready to ship
200mg USD 1,650.00 Ready to ship
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Synonym
GSK2643943A; GSK 2643943A; GSK-2643943A; GSK2643943; GSK 2643943; GSK-2643943;
IUPAC/Chemical Name
(E)-2-amino-6-(3-fluorostyryl)-1H-indole-3-carbonitrile
InChi Key
CGXBPMZRTMXEIA-SNAWJCMRSA-N
InChi Code
InChI=1S/C17H12FN3/c18-13-3-1-2-11(8-13)4-5-12-6-7-14-15(10-19)17(20)21-16(14)9-12/h1-9,21H,20H2/b5-4+
SMILES Code
N#CC1=C(N)NC2=C1C=CC(/C=C/C3=CC=CC(F)=C3)=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
>3 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:
GSK2643943A is a deubiquitylating enzyme (DUB) inhibitor, with an IC50 of 160 nM for USP20/Ub-Rho.
In vitro activity:
TBD
In vivo activity:
TBD
Solvent mg/mL mM
Solubility
DMSO 90.0 324.56
Ethanol 8.0 28.85
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 277.30 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:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
Kemp M. Chapter three-recent advances in the discovery of deubiquitinating enzyme inhibitors. Progress in Medicinal Chemistry. 2016;55:149-192