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(R)-GNE-140 LDHA Inhibitor

Cat.No.S6675

(R)-GNE-140 is an inhibitory agent for LDHA, LDHB, and LDHC, with IC50 values ​​of 3 nM and 5 nM for LDHA and LDHB, respectively. (R)-GNE-140 is 18 times more potent than its S isomer.
(R)-GNE-140 Dehydrogenase inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 499.04

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Quality Control

Batch: Purity: 99.65%
99.65

Solubility

In vitro
Batch:

DMSO : 30 mg/mL (60.11 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
Batch:

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Chemical Information, Storage & Stability

Molecular Weight 499.04 Formula

C25H23ClN2O3S2

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 2003234-63-5 -- Storage of Stock Solutions

Synonyms N/A Smiles C1COCCN1C2=CC=C(C=C2)C3(CC(=C(C(=O)N3)SC4=CC=CC=C4Cl)O)C5=CSC=C5

Mechanism of Action

Targets/IC50/Ki
LDHA
(Cell-free assay)
3 nM
LDHB
(Cell-free assay)
5 nM
In vitro

(R)-GNE-140 inhibits proliferation in 37 of 347 cancer cell lines tested at a potency cut off of 5 μM. This compound exhibits inhibition with two chondrosarcoma (bone) cancer cell lines that harbored IDH1 mutations (IC50 = 0.8μM). This chemical has submicromolar MiaPaca2 potency and inhibits proliferation in 11% of cancer cell lines in a broad panel.

In vivo

(R)-GNE-140 presents a low Clp, and also had high bioavailability when dosed orally at 5 mg/kg to mice. At higher oral doses, ranging from 50 to 200 mg/kg, this compound displays greater in vivo exposure.

References

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