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1333377-65-3

CHR-6494

CAS: 1333377-65-3

Molecular Formula: C16H16N6

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1333377-65-3 - Names and Identifiers

Name CHR-6494
Synonyms CHR-6494
CHR 6494 trifluoroacetate salt
CHR-6494 trifluoroacetate salt
Haspin Kinase Inhibitor, CHR-6494
3-(1H-indazol-5-yl)-N-propyliMidazo[1,2-b]pyridazin-6-aMine
3-(1H-Indazol-5-yl)-N-propylimidazo[1,2-b]pyridazin-6-amine trifluoroacetate salt
3-(1H-Indazol-5-yl)-N-propyl-imidazo[1,2-b]pyridazin-6-amine trifluoroacetate salt
CHR-6494 3-(1H-indazol-5-yl)-N-propyliMidazo[1,2-b]pyridazin-6-aMine
CAS 1333377-65-3

1333377-65-3 - Physico-chemical Properties

Molecular FormulaC16H16N6
Molar Mass292.34
Density1.39±0.1 g/cm3(Predicted)
Solubility DMSO: soluble5mg/mL, clear (warmed)
Appearancepowder
Colorwhite to beige
pKa13.24±0.40(Predicted)
Storage Condition2-8°C
In vitro study CHR-6494 is a potent inhibitor of haspin, inhibiting histone H3T3 phosphorylation, with an IC 50 of 2 nM. CHR-6494 does not modify H3S10 and H328 phosphorylation levels, and shows no significantly inhibitory effects on other protein kinases such as Aurora B kinase. CHR-6494 dose-dependently inhibits the growth of cancer cells, such as HCT-116, HeLa, MDA-MB-231, and Wi-38 cell, with IC 50 s of 500 nM, 473 nM, 752 nM and 1059 nM, respectively. CHR-6494 (500 nM) produces a mitotic catastrophe with abnormal morphology of the mitotic spindle and centrosome amplification, and upregulates the spindle assembly checkpoint protein BUB1 and the marker of mitotic arrest cyclin B1. CHR-6494 exhibits inhibitory activities against melanoma cell lines, including BRAFV600E mutants, NRAS mutants, and wild type cells, with IC 50 s ranging from 396 nM to 1229 nM. CHR-6494 (300 nM and 600 nM) induces apoptosis, increases caspase 3/7 activity by 3- and 6-fold, respectively in COLO-792 cells, and to 8.5- and 16-fold in RPMI-7951 cells. CHR-6494 in combination with MEK inhibitors synergistically inhibits viability of melanoma cells, enhances apoptosis in melanoma cells, modulates cell cycle progression independently by arresting melanoma cells at different phases, and suppresses migration of melanoma cells.
In vivo study CHR-6494 (50 mg/kg, i.p.) inhibits the growth of tumor and cuases no obvious body weight change in nude mice bearing HCT-116 human colorectal cancer cells.

1333377-65-3 - Risk and Safety

WGK Germany3

1333377-65-3 - Preparation solution concentration reference

 1mg5mg10mg
1 mM3.421 ml17.103 ml34.207 ml
5 mM0.684 ml3.421 ml6.841 ml
10 mM0.342 ml1.71 ml3.421 ml
5 mM0.068 ml0.342 ml0.684 ml
Last Update:2024-01-02 23:10:35

1333377-65-3 - Reference Information

biological activity CHR-6494 is an effective haspin inhibitor, which can inhibit the phosphorylation of histone H3T3 with an IC50 value of 2 nM.
target IC50: 2 nM (haspin)
in vitro study CHR-6494 is a potent inhibitor of haspin, inhibiting histone H3T3 phosphorylation, with an IC 50 of 2 nM. CHR-6494 does not modify H3S10 and H328 phosphorylation levels, and shows no significantly inhibitory effects on other protein kinases such as Aurora B kinase. CHR-6494 dose-dependently inhibits the growth of cancer cells, such as HCT-116, heLa, MDA-MB-231, and Wi-38 cell, with IC 50 s of 500   nM, 473   nM, 752   nM and 1059 nM, respectively. CHR-6494 (500 nM) produces a mitotic catastrophe with abnormal morphology of the mitotic spindle and centrosome amplification, and upregulates the spindle assembly checkpoint protein BUB1 and the marker of mitotic arrest cyclin B1. CHR-6494 exhibits inhibitory activities against melanoma cell lines, including BRAFV600E mutants, NRAS mutants, and wild type cells, with IC 50 s ranging from 396 nM to 1229 nM. CHR-6494 (300 nM and 600 nM) induces apoptosis, increases caspase 3/7 activity by 3- and 6-fold, respectively in COLO-792 cells, and to 8.5- and 16-fold in RPMI-7951 cells. CHR-6494 in combination with MEK inhibitors synergistically inhibits viability of melanoma cells, enhances apoptosis in melanoma cells, modulates cell cycle progression independently by arresting melanoma cells at different phases, and suppresses migration of melanoma cells.
in vivo study CHR-6494 (50   mg/kg, I. p.) inhibits the growth of tumor and cuases no obvious body weight change in nude mice bearing HCT-116 human colorectal cancer cells.
Last Update:2024-04-09 02:00:01
1333377-65-3
Supplier List
Shanghai Amole Biotechnology Co., Ltd.
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Product Name: 3-(1H-Indazol-5-yl)-N-propylimidazo[1,2-b]pyridazin-6-amine Request for quotation
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Shanghai Yuanye Bio-Technology Co., Ltd.
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Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: 3-(1H-Indazol-5-yl)-N-propylimidazo[1,2-b]pyridazin-6-amine Request for quotation
CAS: 1333377-65-3
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
Shanghai Macklin Biochemical Co., Ltd
Spot supply
Product Name: CHR-6494  Visit Supplier Webpage Request for quotation
CAS: 1333377-65-3
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: CHR-6494 Visit Supplier Webpage Request for quotation
CAS: 1333377-65-3
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
WhatsApp: +86-18621343501
MedChemExpress (MCE)
Spot supply
Product Name: CHR-6494 Visit Supplier Webpage Request for quotation
CAS: 1333377-65-3
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
Shanghai Yuanye Bio-Technology Co., Ltd.
Spot supply
Product Name: CHR-6494 Visit Supplier Webpage Request for quotation
CAS: 1333377-65-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
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