ChemicalBook > CAS DataBase List > SCH900776

SCH900776

Product Name
SCH900776
CAS No.
891494-63-6
Chemical Name
SCH900776
Synonyms
SCH900776(R);SCH 900776, >=98%;SCH900776 USP/EP/BP;SCH 900776 (MK-8776);MK-8776 (SCH 900776);MK-8776 (SCH900776)(S);SCH-900776; SCH 900776; MK-8776.;SCH900776 MK-8776 SCH-900776 MK8776;Inhibitor,MK8776,Checkpoint Kinase (Chk),SCH900776,SCH-900776,inhibit,SCH 900776;6-Bromo-3-(1-methyl-1H-pyrazol-4-yl)-5-(3R)-3-piperidinylpyrazolo[1,5-a]pyrimidin-7-amine
CBNumber
CB72596614
Molecular Formula
C15H18BrN7
Formula Weight
376.25
MOL File
891494-63-6.mol
More
Less

SCH900776 Property

Density 
1.80
storage temp. 
Store at -20°C
solubility 
insoluble in H2O; insoluble in EtOH; ≥18.8 mg/mL in DMSO
form 
A crystalline solid
pka
8.88±0.10(Predicted)
color 
White to off-white
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML3587
Product name
SCH 900776
Purity
≥98% (HPLC)
Packaging
5MG
Price
$99
Updated
2024/03/01
Sigma-Aldrich
Product number
SML3587
Product name
SCH 900776
Purity
≥98% (HPLC)
Packaging
25MG
Price
$399
Updated
2024/03/01
Cayman Chemical
Product number
18131
Product name
SCH 900776
Purity
≥95%
Packaging
500μg
Price
$45
Updated
2024/03/01
Cayman Chemical
Product number
18131
Product name
SCH 900776
Purity
≥95%
Packaging
1mg
Price
$72
Updated
2024/03/01
Cayman Chemical
Product number
18131
Product name
SCH 900776
Purity
≥95%
Packaging
5mg
Price
$241
Updated
2024/03/01
More
Less

SCH900776 Chemical Properties,Usage,Production

Uses

This compound acts as a novel Chk1 inhibitor acting as an anticancer agent.

Biological Activity

sch 900776 is a potent and selective inhibitor of cell cycle checkpoint kinase 1 (chk1), chk2 and cdk3 with ic50 value of 3 nm, 1.5μm and 0.16 μm, respectively.chk is s serine/threonine kinase that senses signal of dna damage and stalls dna replication, and also plays an essential role in the maintenance of replication fork viability during exposure to dna antimetabolites.in balb/c mice, administration of sch 900776 at a dosage of 8mg/kg after gemcitabine treatment can sufficiently induce enhanced tumor pharmacodynamic and regression responses as compared to gemcitabine or sch 900776 alone 1.

in vitro

sch 900776 blocked accumulation of the chk1 ps296 autophosphorylation in a dose-dependent manner. treatment of proliferating ws1 cells with sch 900776 was found to be associated with rapid, dose-dependent accumulation of chk1 ps345, indicating that cycling populations of normal cells induce chk1 ps345 in response to the inhibition of sch 900776 as part of a futile cycle 1.

References

1. guzi tj, paruch k, dwyer mp, et al. targeting the replication checkpoint using sch 900776, a potent and functionally selective chk1 inhibitor identified via high content screening. molecular cancer therapeutics. 2011;10(4):591-602.

SCH900776 Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

SCH900776 Suppliers

MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2782
Advantage
58
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
Creative Enzymes
Tel
--
Fax
--
Email
info@creative-enzymes.com
Country
United States
ProdList
6057
Advantage
58
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Tinib-Tools
Tel
--
Fax
--
Country
United States
ProdList
164
Advantage
0
NE Scientific
Tel
--
Fax
--
Country
United States
ProdList
5030
Advantage
55
ChemieTek
Tel
--
Fax
--
Email
info@chemietek.com
Country
United States
ProdList
219
Advantage
50
Santa Cruz Biotechnology, Inc.
Tel
--
Fax
--
Email
scbt@scbt.com
Country
United States
ProdList
3597
Advantage
60

891494-63-6, SCH900776Related Search:


  • 6-Bromo-3-(1-methyl-1H-pyrazol-4-yl)-5-(3R)-3-piperidinylpyrazolo[1,5-a]pyrimidin-7-amine
  • SCH-900776; SCH 900776; MK-8776.
  • MK-8776 (SCH 900776)
  • SCH 900776 (MK-8776)
  • SCH900776(R)
  • 6-bromo-3-(1-methyl-1H-pyrazol-4-yl)-5-((R)-piperidin-3-yl)pyrazolo[1,5-a]pyrimidin-7-amine
  • SCH 900776, >=98%
  • (R)-6-Bromo-3-(1-methyl-1H-pyrazol-4-yl)-5-(piperidin-3-yl)pyrazolo[1,5-a]pyrimidin-7-amine
  • MK-8776 (SCH900776)(S)
  • Pyrazolo[1,5-a]pyrimidin-7-amine, 6-bromo-3-(1-methyl-1H-pyrazol-4-yl)-5-(3R)-3-piperidinyl-
  • SCH900776 USP/EP/BP
  • SCH900776 MK-8776 SCH-900776 MK8776
  • Inhibitor,MK8776,Checkpoint Kinase (Chk),SCH900776,SCH-900776,inhibit,SCH 900776
  • 6-Bromo-3-(1-methyl-1H-pyrazol-4-yl)-5-(3R)-3-piperidinylpyrazolo[1,5-a]pyrimidin-7-amine , SCH900776
  • 891494-63-6
  • C15H18BrN7
  • Inhibitors