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CCT 137690

CAS No.
1095382-05-0
Chemical Name:
CCT 137690
Synonyms
CS-56;CCT 137690;CCT137690, >=98%;CCT 137690 USP/EP/BP;CCT-137690; CCT137690;3-((4-(6-Bromo-2-(4-(4-methylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-;6-Bromo-7-[4-[(5-methyl-3-isoxazolyl)methyl]-1-piperazinyl]-2-[4-(4-methyl-1-piperazinyl)phenyl]-3H-imidazo[4,5-b]pyridine;6-bromo-7-(4-((5-methylisoxazol-3-yl)methyl)piperazin-1-yl)-2-(4-(4-methylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridine;3H-Imidazo[4,5-b]pyridine, 6-bromo-7-[4-[(5-methyl-3-isoxazolyl)methyl]-1-piperazinyl]-2-[4-(4-methyl-1-piperazinyl)phenyl]-;3-[[4-[6-Bromo-2-[4-(4-methylpiperazin-1-yl)phenyl]-3H-imidazo[4,5-b]pyridin-7-yl]piperazin-1-yl]methyl]-5-methylisoxazole CCT-137690
CBNumber:
CB72561069
Molecular Formula:
C26H31BrN8O
Molecular Weight:
551.48
MDL Number:
MFCD18206879
MOL File:
1095382-05-0.mol
MSDS File:
SDS
Last updated:2023-09-04 15:50:00

CCT 137690 Properties

Density 1.424
storage temp. Store at -20°C
solubility insoluble in H2O; insoluble in EtOH; ≥6.89 mg/mL in DMSO
form solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317-H319
Precautionary statements  P280-P305+P351+P338

CCT 137690 price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 15552 CCT137690 ≥98% 1095382-05-0 5mg $110 2024-03-01 Buy
Cayman Chemical 15552 CCT137690 ≥98% 1095382-05-0 10mg $142 2024-03-01 Buy
Cayman Chemical 15552 CCT137690 ≥98% 1095382-05-0 50mg $648 2024-03-01 Buy
Tocris 4291 CCT137690 ≥98%(HPLC) 1095382-05-0 50 $979 2021-12-16 Buy
Tocris 4291 CCT137690 ≥98%(HPLC) 1095382-05-0 10 $271 2021-12-16 Buy
Product number Packaging Price Buy
15552 5mg $110 Buy
15552 10mg $142 Buy
15552 50mg $648 Buy
4291 50 $979 Buy
4291 10 $271 Buy

CCT 137690 Chemical Properties,Uses,Production

Uses

CCT 137690 is used in the treatment of acute myeloid leukemia.

Biological Activity

cct137690 is an orally bioavailable inhibitor of aurora kinases with ic50 values in a range from 15 to 25 nm [1].aurora kinase is a family of serine/threonine kinases including aurora-a, b and c. they play important roles in the regulation of mitosis and take participate in the causation and progression of various tumors including ovarian, breast, glioma and colon. therefore aurora kinases have been regarded as anti-cancer targets in cancer chemotherapeutics.cct137690 is a selective small-molecular inhibitor of aurora kinases and showed anti-tumor activities both in vitro and in vivo. besides that, cct137690 exerted good stability in mouse liver microsomes [1].when tested toward a panel of 94 kinases, cct137690inhibited 80% activities of veg-fr, aurora-a, and fgf-r1 at concentration of 1 μm. it suppressed the phosphorylation of histone h3 caused by aurora-b. the ic50 values of cct137690 against aurora-b and c were 25 and 19 nm, respectively. cct137690 showed potent anti-proliferation effects on various kinds of tumors such as a2780 ovarian tumor cell (ic50 value of 140 nm), sw620 (ic50 value of 300 nm) and sw48 colon carcinoma (ic50 value of 157 nm). it caused cell cycle perturbations. in addition, cct137690 was found to have synergistic effects with radiotherapy. it increased the sensitivity of sw620 cells to radiation. the combination treatment resulted in much more cell death through apoptosis [1 and 2].in mice model bearing sw620 xenografts, administration of cct137690slowed the growth of tumors without observed toxicity. the ratio of treat/control group based on tumor weight was 37% at the dose of 75 mg/kg. besides that, cct137690 was found to significantly reduced neuroblastoma tumor mass in mycn transgenic mice, which meant cct137690 could benefit patients with mycn-amplified neuroblastoma [1 and 3].

References

[1] bavetsias v, large j m, sun c, et al. imidazo [4, 5-b] pyridine derivatives as inhibitors of aurora kinases: lead optimization studies toward the identification of an orally bioavailable preclinical development candidate. journal of medicinal chemistry, 2010, 53(14): 5213-5228.
[2] wu x, liu w, cao q, et al. inhibition of aurora b by cct137690 sensitizes colorectal cells to radiotherapy. j expclin cancer res, 2014, 33(1): 13.
[3] faisal a, vaughan l, bavetsias v, et al. the aurora kinase inhibitor cct137690 downregulates mycn and sensitizes mycn-amplified neuroblastoma in vivo. molecular cancer therapeutics, 2011, 10(11): 2115-2123.

942949-26-0
27913-99-1
1095382-05-0
Synthesis of CCT 137690 from Ethanamine, N-[(3,5-dichlorophenyl)methylene]-2,2-diethoxy- and 4-(4-Methylpiperazino)benzaldehyde

CCT 137690 Preparation Products And Raw materials

Raw materials

Preparation Products

CCT 137690 Suppliers

Global( 93)Suppliers
Supplier Tel Email Country ProdList Advantage
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
TargetMol Chemicals Inc.
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HANGZHOU CLAP TECHNOLOGY CO.,LTD
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Dideu Industries Group Limited
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Zhejiang J&C Biological Technology Co.,Limited
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InvivoChem
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Nantong HI-FUTURE Biology Co., Ltd.
+undefined18051384581 sales@chemhifuture.com China 3136 58
Hebei Miaoyin Technology Co.,Ltd
+86-17367732028 +86-17367732028 kathy@hbyinsheng.com China 3582 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58

CCT 137690 Spectrum

CCT 137690 6-bromo-7-(4-((5-methylisoxazol-3-yl)methyl)piperazin-1-yl)-2-(4-(4-methylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridine 3-[[4-[6-Bromo-2-[4-(4-methylpiperazin-1-yl)phenyl]-3H-imidazo[4,5-b]pyridin-7-yl]piperazin-1-yl]methyl]-5-methylisoxazole CCT-137690 CCT137690, >=98% 3-((4-(6-Bromo-2-(4-(4-methylpiperazin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1- 6-Bromo-7-[4-[(5-methyl-3-isoxazolyl)methyl]-1-piperazinyl]-2-[4-(4-methyl-1-piperazinyl)phenyl]-3H-imidazo[4,5-b]pyridine CS-56 CCT-137690; CCT137690 3H-Imidazo[4,5-b]pyridine, 6-bromo-7-[4-[(5-methyl-3-isoxazolyl)methyl]-1-piperazinyl]-2-[4-(4-methyl-1-piperazinyl)phenyl]- CCT 137690 USP/EP/BP 1095382-05-0 C26H31BrN8O Inhibitors Inhibitor