Anticancer agent 122

SKU:BHB21901961
Overview
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Anticancer agent 122 (CAS 2924532-50-1) is a human lactate dehydrogenase A inhibitor. Relevant to Metabolic Enzyme/Protease research. Molecular formula C18H15ClN2O2S, molecular weight 358.84 g/mol.
CAS Number 2924532-50-1
Molecular Weight 358.84 g/mol
Storage See Certificate of Analysis
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Catalog no. Size
HY-154866-50MG 50 mg
HY-154866-100MG 100 mg
HY-154866-250MG 250 mg
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Field Specification
CAS no. 2924532-50-1
Applications
  • Functional Assay (In Vitro)
Molecular weight 358.84
Molecular formula C18H15ClN2O2S
SMILES O=C(OC)C/N=C1SC=C(C2=CC=CC=C2)N/1C3=CC=C(Cl)C=C3
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-154866
Main SKU BHB21901961
Inhibitors

Compound Overview

Anticancer agent 122 is an inhibitor of human lactate dehydrogenase A (hLDHA) reported to have good anticancer activity, and it can be applied in anticancer research[1]. It has a molecular formula of C18H15ClN2O2S and a molecular weight of 358.84 g/mol.

Physical & Chemical Properties

CAS Number 2924532-50-1
Molecular Formula C18H15ClN2O2S
Molecular Weight 358.84 g/mol
SMILES O=C(OC)C/N=C1SC=C(C2=CC=CC=C2)N/1C3=CC=C(Cl)C=C3
Signaling Pathway Metabolic Enzyme/Protease
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Sharma D, et.al. Design and Synthesis of Thiazole Scaffold-Based Small Molecules as Anticancer Agents Targeting the Human Lactate Dehydrogenase A Enzyme. ACS Omega. 2023 May 10;8(20):17552-17562.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vitro

Anticancer agent 122 (0-100 μM; 72 hours) inhibits the liver cancer cell line HepG2 and the cervical cancer cell line SiHa, with IC50s of 5.15 μM and 1.65 μM, respectively, while showing no noticeable toxicity in the human embryonic kidney cell line HEK293[1].

Cell Cytotoxicity Assay[1]

Cell LineHEK293, HepG2 and SiHa
Concentration0-100 μM
Incubation Time72 hours
ResultInhibited liver cancer cell line HepG2 cells and cervical cancer cell line SiHa cells with IC50s of 5.15 μΜ and 1.65 μΜ,respectively. Had not noticeable toxicity in HEK293.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price listed?
A.Every size of this product is quoted on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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