ChemicalBook >> CAS DataBase List >>MK-2206 2HCl

MK-2206 2HCl

CAS No.
1032350-13-2
Chemical Name:
MK-2206 2HCl
Synonyms
MK-2206;MK-2206 Dihydrochloride;CS-260;MK-2206 2HCl;MK-2206 HCl salt;MK-2206 2HCL;MK2206;MK-2206 2HCl ,S1078;Benodanil Impurity 9;MK-2206 2HCl USP/EP/BP;MK 2206 (hydrochloride)
CBNumber:
CB72489901
Molecular Formula:
C25H22ClN5O
Molecular Weight:
443.94
MDL Number:
MFCD14584463
MOL File:
1032350-13-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-20 20:20:01

MK-2206 2HCl Properties

Melting point >255°C (dec.)
storage temp. -20°C
solubility Soluble in DMSO (up to 10 mg/ml with warming)
form Yellow powder.
color Yellow
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKey LFYOZCBFOSSLNJ-UHFFFAOYSA-N
SMILES O=C1NN=C2C3=CC(C4C=CC=CC=4)=C(C4C=CC(C5(CCC5)N)=CC=4)N=C3C=CN12.Cl
FDA UNII Q34I3E28IO

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2933998090
NFPA 704
0
2 0

MK-2206 2HCl price More Price(82)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 11593 MK-2206 (hydrochloride) ≥98% 1032350-13-2 1mg $48 2026-04-30 Buy
Cayman Chemical 11593 MK-2206 (hydrochloride) ≥98% 1032350-13-2 5mg $94 2026-04-30 Buy
Cayman Chemical 11593 MK-2206 (hydrochloride) ≥98% 1032350-13-2 10mg $117 2026-04-30 Buy
Cayman Chemical 11593 MK-2206 (hydrochloride) ≥98% 1032350-13-2 25mg $151 2026-04-30 Buy
Biosynth FA26026 MK 2206 dihydrochloride 1032350-13-2 50mg $317 2026-06-04 Buy
Product number Packaging Price Buy
11593 1mg $48 Buy
11593 5mg $94 Buy
11593 10mg $117 Buy
11593 25mg $151 Buy
FA26026 50mg $317 Buy

MK-2206 2HCl Chemical Properties,Uses,Production

Description

MK-2206 (CAS 1032350-13-2) is a potent and selective allosteric inhibitor of Akt (IC50’s: Akt1 = 5 nM, Akt2 = 12 nM, Akt3 = 65 nM) that enhances thein vitroandin vivoantitumor efficacy of several standard chemotherapeutic agents.1It was able to decrease insulin-stimulated glucose uptake, glycogen synthesis and glycogen synthase activity in rat muscle.2MK-2206 induced G1-phase cycle arrest and sensitized HepG2 hepatocellular carcinoma cells to TRAIL-induced apoptosis.3

Uses

A highly selective inhibitor of Akt. Akt1, IC50=8 nM; Akt2, IC50=12 nM; Akt3, IC50=65 nM.

Uses

AZD 6244 and MK 2206 are targeted small-molecule drugs that inhibit MEK and AKT responses. The combination of AZD6244 and MK2206 has a significant synergistic effect on tumor growth in vitro and in vivo and leads to increased survival rates in mice bearing highly aggressive human lung tumors. Antitumor agents. Potent AKT inhibitor.

in vivo

Both MK-2206 dihydrochloride (MK-2206 (2HCl)) doses (oral gavage; 480 mg/kg once a week and 240 mg/kg three times a week; for 2 weeks) can inhibit the growth of human CNE-2 xenografts in nude mice. No other obvious toxicity is observed in mice[2].
MK-2206 dihydrochloride (orally; 120 mg/kg; alternate days; for 3 weeks) significantly inhibits tumor growth in 3-5 week old athymic nude mice with GEO colon carcinoma cells[3].

Animal Model:Four- to 6-week-old male BALB/c nude mice with CNE-2 xenografts[2]
Dosage:240 mg/kg and 480 mg/kg
Administration:Oral gavage; 240 mg/kg for three times a week; 480 mg/kg for once a week; for 2 weeks
Result:Both doses inhibited the growth of human CNE-2 xenografts in nude mice.

target

Akt1

IC 50

Akt1: 8 nM (IC50); Akt2: 12 nM (IC50); Akt3: 65 nM (IC50)

storage

-20°C

References

[1] HIROSHI HIRAI. MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo.[J]. Molecular Cancer Therapeutics, 2010, 9 7: 1956-1967. DOI:10.1158/1535-7163.mct-09-1012
[2] YU-CHIANG LAI. A novel PKB/Akt inhibitor, MK-2206, effectively inhibits insulin-stimulated glucose metabolism and protein synthesis in isolated rat skeletal muscle.[J]. Biochemical Journal, 2012, 447 1: 137-147. DOI:10.1042/bj20120772
[3] PENG JIAO. MK-2206 induces cell cycle arrest and apoptosis in HepG2 cells and sensitizes TRAIL-mediated cell death.[J]. Molecular and Cellular Biochemistry, 2013, 382 1-2: 217-224. DOI:10.1007/s11010-013-1737-0

MK-2206 2HCl Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 268)Suppliers
Supplier Tel Email Country ProdList Advantage
Xianning Shen Lan Biomedical Research and Development Co., Ltd. 18171815831 1341138380@qq.com China 4572 58
TargetMol Chemicals Inc. 021-021-33632979 15002134094 marketing@targetmol.com China 7993 58
Wuhan Augda Biotechnology Co., Ltd 15071299552 262933239@qq.com China 7200 58
Shanghai jerryxing Biomedical Technology Co., Ltd 17521512546 17721492509 460170712@qq.com China 4965 58
Shanghai Boyle Chemical Co., Ltd. sales@boylechem.com China 2915 55
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61
Shangchem Co., Ltd. +86-21-68182121 China 881 52
WUHAN SUN-SHINE BIO-TECHNOLOGY Co., Ltd. 17702719238 sales@sun-shinechem.com China 1197 64
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50

View Lastest Price from MK-2206 2HCl manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
MK-2206 dihydrochloride pictures 2026-08-20 MK-2206 dihydrochloride
1032350-13-2
$30.00-64.00 99.73% 10g TargetMol Chemicals Inc.
MK-2206 2HCl pictures 2023-09-07 MK-2206 2HCl
1032350-13-2
$30.00 1kg 99% 1000t/year Anhui Ruihan Technology Co., Ltd
MK-2206 2HCl pictures 2019-07-06 MK-2206 2HCl
1032350-13-2
$2.00 1kg 99% 100kg Career Henan Chemical Co
  • MK-2206 2HCl pictures
  • MK-2206 2HCl
    1032350-13-2
  • $30.00
  • 99%
  • Anhui Ruihan Technology Co., Ltd

MK-2206 2HCl Spectrum

8-[4-(1-Aminocyclobutyl)phenyl]-9-phenyl-1,2,4-triazolo[3,4-f][1,6]naphthyridin-3(2H)-one dihydrochloride MK 2206 2HCL;MK2206 2HCL CS-260 MK2206; MK-2206; MK 2206; MK2206 DIHYDROCHLORIDE; MK2206 HCL. 8-[4-(1-AMinocyclobutyl)phenyl]-9-phenyl-1,2,4-triazolo[3,4-f][1,6]naphthyridin-3(2H)-one Hydrochloride 8-(4-(1-aminocyclobutyl)phenyl)-9-phenyl-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2H)-one 8-[4-(1-Aminocyclobutyl)phenyl]-9-phenyl-1,2,4-triazolo[3,4-f][1,6]naphthyridin-3(2H)-one dihydrochloride MK-2206 MK-2206 8-[4-(1-Aminocyclobutyl)phenyl]-9-phenyl-1,2,4-triazolo[3,4-f][1,6]naphthyridin-3(2H)-one dihydrochloride MK 2206 (hydrochloride) MK-2206 2HCl MK-2206 dihydrochloride, >=98% MK-2206 2HCL;MK2206 8-[4-(1-Aminocyclobutyl)phenyl]-9-phenyl-1,2,4-triazolo[3,4-f][1,6]naphthyridin-3(2H)-one dihydrochlorideMK-2206 Dihydrochloride MK-2206 HCl salt 1,2,4-Triazolo[3,4-f][1,6]naphthyridin-3(2H)-one, 8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-, hydrochloride (1:2) (8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3-one) dihydrochloride MK 2206 dihydrochloride, 98%, an allosteric Akt inhibitor 8-[4-(1-AMINOCYCLOBUTYL)PHENYL]-9-PHENYL-1,2,4-TRIAZOLO[3,4-F][1,6]NAPHTHYRIDIN-3(2H)-ONE 2HCL MK 2206 2HCL;MK2206 2HCL;MK-2206 DIHYDROCHLORIDE;MK2206 DIHYDROCHLORIDE MK-2206 2HCl USP/EP/BP MK-2206 2HCl/MK-2206 dihydrochloride MK-2206 dihydrochloride MK2206 MK-2206 DIHYDROCHLORIDE SALT (2XHCL SALT) Benodanil Impurity 9 MK-2206 dihydrochloride, 10 mM in DMSO MK-2206 2HCl ,S1078 MK-2206 MK-2206 Dihydrochloride 1032350-13-2 C25H21N5O2HCl C25H23Cl2N5O C25H21N5O2ClH Inhibitor PI3K/Akt/mTOR Inhibitors Akt mTOR PI3K Amines Heterocycles Intermediates & Fine Chemicals Pharmaceuticals