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KA2507 monohydrochloride

CAS No.
2972712-63-1
Chemical Name:
KA2507 monohydrochloride
Synonyms
KA2507 monohydrochloride;Benzamide, 4-[(di-2-pyrazinylamino)methyl]-N-hydroxy-, hydrochloride (1:1)
CBNumber:
CB613259372
Molecular Formula:
C16H14N6O2.ClH
Molecular Weight:
358.78
MDL Number:
MOL File:
2972712-63-1.mol
MSDS File:
SDS
Last updated:2026-07-16 07:06:08

KA2507 monohydrochloride Properties

form Solid
color Off-white to light yellow

KA2507 monohydrochloride price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
DC Chemicals DC66334 KA2507 monohydrochloride >98% 2972712-63-1 100mg $550 2026-05-24 Buy
DC Chemicals DC66334 KA2507 monohydrochloride >98% 2972712-63-1 250mg $850 2026-05-24 Buy
DC Chemicals DC66334 KA2507 monohydrochloride >98% 2972712-63-1 1g $1800 2026-05-24 Buy
Product number Packaging Price Buy
DC66334 100mg $550 Buy
DC66334 250mg $850 Buy
DC66334 1g $1800 Buy

KA2507 monohydrochloride Chemical Properties,Uses,Production

Uses

KA2507 hydrochloride is a potent and highly selective inhibitor of HDAC6 (IC50=2.5 nM) with no significant toxicities. KA2507 hydrochloride shows antitumor efficacy and immune modulatory effects[1].

in vivo

KA2507 hydrochloride (100-200 mg/kg; p.o.; daily; for 20 days) inhibits tumor growth in the syngeneic B16-F10 mouse melanoma model[1].
KA2507 hydrochloride also demonstrates antitumor efficacy in CT26 and MC38 colorectal cancer models[1].
Analysis of tumor samples also indicates modulation of biomarkers of antitumor immunity at efficacious dosing, with KA2507 hydrochloride administration resulting in reduced STAT3 activation (as measured by phospho-STAT3, an important suppressor of the antitumor immune response), reduced PD-L1 expression, and increased expression of MHC class I[1].
KA2507 hydrochloride exhibits poor oral bioavailability (mice 15%) and Cmax (mice 300 ng/mL) following oral administration (mice 200 mg/kg)[1].

Animal Model:Male C57BL/6 mice, B16-F10 melanoma model[1]
Dosage:100 mg/kg, 200 mg/kg,
Administration:P.o.; once a day for 20 days
Result:Inhibited tumor growth in the syngeneic B16-F10 mouse melanoma model.
Animal Model:Male C57BL/6 mice, B16-F10 melanoma model[1]
Dosage:200 mg/kg (Pharmacokinetic Analysis)
Administration:Oral administration
Result:Oral bioavailability (15%), Cmax (300 ng/mL).

References

[1] Tsimberidou AM, et al. Preclinical Development and First-in-Human Study of KA2507, a Selective and Potent Inhibitor of Histone Deacetylase 6, for Patients with Refractory Solid Tumors. Clin Cancer Res. 2021;27(13):3584-3594. DOI:10.1158/1078-0432.CCR-21-0238

KA2507 monohydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

KA2507 monohydrochloride Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 9920 65
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Shanghai SuperLan Chemcial Technique Centre 0-2022843681 15618226720 chaolaichem@foxmail.com China 10000 58
Jinan Jiuli Biotechnology Co. , Ltd. 15865264761 486064515@qq.com China 4960 58
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 psaitong@jm-bio.com China 27626 58
Zhejiang Huida Biotech Co., Ltd. 0571-89903022 18679456698 zilong@hizyme.com China 7853 58
TargetMol Chemicals Inc. 13564774135 marketing@targetmol.com United States 19950 58

View Lastest Price from KA2507 monohydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
KA2507 monohydrochloride pictures 2026-07-15 KA2507 monohydrochloride
10g TargetMol Chemicals Inc.
KA2507 monohydrochloride Benzamide, 4-[(di-2-pyrazinylamino)methyl]-N-hydroxy-, hydrochloride (1:1) 2972712-63-1