2-Bromobenzo[d]thiazole-6-carboxylic+acid
Supplier:
BeanTown Chemical
Description:
CAS: 125572-95-4; EC No: 236-308-9; MDL No: MFCD00149243
Crystalline/Powder; Molecular Formula: C14H22N2O8·H2O ; MW: 364.35
Melting Point: 213-216°
Supplier:
Matrix Scientific
Description:
5-(4-Fluorophenyl)-2, 2-Dimethyl-2, 3-Dihydro-4H-Imidazol-4-One, MF=C11H11FN2O, MW=206.22, CAS=899926-79-5, 1G
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 047059-1G , MDL Number: MFCD08689725
Supplier:
AMBEED, INC
Description:
7-Bromo-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one 95%
Catalog Number:
(101843-158)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 037339-500MG , MDL Number: MFCD07357406
Catalog Number:
(76480-808)
Supplier:
AAT BIOQUEST INC
Description:
5(6)-TAMRA cadaverine is a building block for developing fluoresceinated bioconjugates.
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Supplier:
TCI America
Description:
CAS Number: 98319-26-7
MDL Number: MFCD00869737 Molecular Formula: C23H36N2O2 Molecular Weight: 372.55 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 253
Catalog Number:
(102837-792)
Supplier:
Matrix Scientific
Description:
3-(Imidazol-1-yl)pyrazine-2-carboxylic acid ≥97%
Catalog Number:
(TCH1218-1G)
Supplier:
TCI America
Description:
CAS Number: 186788-38-5
Molecular Formula: C13H24N2O
Molecular Weight: 224.35
Purity/Analysis Method: <gt/>95.0% (GC)
Form: Crystal
Melting point (°C): 67
Supplier:
Adipogen
Description:
Antagonizing the Chk1-mediated cell cycle checkpoints has emerged as an attractive target for anticancer therapy. If Chk1 activity is blocked, DNA-damaged or spindle-disrupted cells would exit cell cycle arrest before full repair and subsequently undergo mitotic catastrophe or cell death. Chk1 inhibitors consequently increase the therapeutic index of DNA-damaging or antimitotic agents as well. PF-0477736 is a selective, potent ATP-competitive Chk1 inhibitor, derived from PF-0394691, inhibits Chk1 (Ki, 0.49nM) and Chk2 (Ki, 47nM) in vitro. In tests, PF-0477736 was identified as a potent, selective ATP-competitive small-molecule inhibitor that inhibits Chk1 with a Ki of 0.49nM. PF-0477736 abrogates cell cycle arrest induced by DNA damage and enhances cytotoxicity of clinically important chemotherapeutic agents, including gemcitabine and carboplatin. In xenografts, PF-0477736 enhanced the antitumor activity of gemcitabine in a dose-dependent manner. PF-0477736 combinations were well tolerated with no exacerbation of side effects commonly associated with cytotoxic agents.
Supplier:
Strem Chemicals Inc
Description:
cataCXium, Phosphine
Supplier:
Matrix Scientific
Description:
N-(1,4,5,6-Tetrahydrocyclopenta-[d]imidazol-2-yl)guanidine sulfate
Supplier:
TCI America
Description:
1-(2,6-Diisopropylphenyl)imidazole, Purity: >98.0%(T), CAS number: 25364-47-0, Molecular Formula: C15H20N2, Molecular Weight: 228.34, Form: Crystal- Powder, White - Almost white, Size: 1G
Catalog Number:
(101835-814)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 033506-500MG , MDL Number: MFCD04971002
Supplier:
TCI America
Description:
CAS Number: 298-46-4
MDL Number: MFCD00005073 Molecular Formula: C15H12N2O Molecular Weight: 236.27 Purity/Analysis Method: >97.0% (N) Form: Crystal Melting point (°C): 191
Catalog Number:
(77620-636)
Supplier:
AMBEED, INC
Description:
(R)-6,7-Dihydro-5H-pyrrolo[1,2-a]imidazol-7-ol ≥95%
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