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1,3-Diphenylpropane
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1,3-Diphenylpropane
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.
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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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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