Glyoxalase I inhibitor | CAS#174568-92-4 | GLO1 inhibitor

MedKoo Cat#: 462450 | Name: Glyoxalase I inhibitor

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Description:

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

Glyoxalase I inhibitor (free base) is a potent Glyoxalase I (GLO1) inhibitor and a candidate for anticancer agents.

Chemical Structure

Glyoxalase I inhibitor

CAS#174568-92-4

Theoretical Analysis

MedKoo Cat#: 462450

Name: Glyoxalase I inhibitor

CAS#: 174568-92-4

Chemical Formula: C21H29BrN4O8S

Exact Mass: 576.0889

Molecular Weight: 577.45

Elemental Analysis: C, 43.68; H, 5.06; Br, 13.84; N, 9.70; O, 22.17; S, 5.55

Price and Availability

Size	Price	Availability	Quantity
5mg	USD 750.00	2 Weeks
10mg	USD 1,250.00	2 Weeks

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Related CAS #

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Synonym

Glyoxalase I inhibitor

IUPAC/Chemical Name

ethyl N5-((R)-3-(((4-bromophenyl)(hydroxy)carbamoyl)thio)-1-((2-ethoxy-2-oxoethyl)amino)-1-oxopropan-2-yl)-L-glutaminate

InChi Key

PYPKSBBTQSNXLR-HOTGVXAUSA-N

InChi Code

InChI=1S/C21H29BrN4O8S/c1-3-33-18(28)11-24-19(29)16(25-17(27)10-9-15(23)20(30)34-4-2)12-35-21(31)26(32)14-7-5-13(22)6-8-14/h5-8,15-16,32H,3-4,9-12,23H2,1-2H3,(H,24,29)(H,25,27)/t15-,16-/m0/s1

SMILES Code

N[C@H](C(OCC)=O)CCC(N[C@@H](CSC(N(O)C1=CC=C(Br)C=C1)=O)C(NCC(OCC)=O)=O)=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

>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

Product Data

Product Data

Instruction

View handling instruction

Biological target:

Glyoxalase I inhibitor (free base) is a potent Glyoxalase I (GLO1) inhibitor, candidate for anticancer agents.

In vitro activity:

TBD

In vivo activity:

TBD

	Solvent	mg/mL	mM
Solubility
	DMSO	110.0	190.49

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 577.45 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

Formulation protocol:

TBD

In vitro protocol:

TBD

In vivo protocol:

TBD

1: Bollong MJ, Lee G, Coukos JS, et al. A metabolite-derived protein modification integrates glycolysis with KEAP1-NRF2 signalling. Nature. 2018;562(7728):600-604. doi:10.1038/s41586-018-0622-0