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2\\\\\\\'-Deoxyguanosine+hydrate

74,817  results were found

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Description:   (R)-4-(Pyrrolidin-3-yl)morpholine dihydrochloride, Purity: 97%, CAS Number: 913702-38-2, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 100MG
Catalog Number: 76660-594
Supplier: AMBEED, INC



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Description:   Benzyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate, Purity: 98%, CAS Number: 315718-05-9, Appearance: Liquid or Solid or Semi-solid or lump, Storage: Inert atmosphere, Room Temperature, Size: 5g
Catalog Number: 77243-542
Supplier: AMBEED, INC



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Description:   Matrix Scientific Part Number: 036386-500MG , MDL Number: MFCD12026897
Catalog Number: 101841-258
Supplier: Matrix Scientific



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Description:   Matrix Scientific Part Number: 055604-100MG , MDL Number: MFCD15530302
Catalog Number: 101909-764
Supplier: Matrix Scientific



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Description:   Matrix Scientific Part Number: 055547-100MG , MDL Number: MFCD15530272
Catalog Number: 101909-650
Supplier: Matrix Scientific



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Description:   5-(N,N-Dimethylsulfamoyl)-N-(5-methylthiazol-2-yl)-2-(pyrrolidin-1-yl)benzamide 99%
Catalog Number: 76656-122
Supplier: AMBEED, INC


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Description:   1-[4-(Trifluoromethyl)benzyl]pyrrolidine-3-carboxylic acid ≥97%
Catalog Number: 102838-140
Supplier: Matrix Scientific



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Description:   Matrix Scientific Part Number: 037498-500MG , MDL Number: MFCD01217237
Catalog Number: 101843-538
Supplier: Matrix Scientific



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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.
Catalog Number: 102992-560
Supplier: Adipogen



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Description:   CAS Number: 139015-33-1
MDL Number: MFCD00191461
Molecular Formula: C5H12N2
Molecular Weight: 100.17
Purity/Analysis Method: >98.0% (GC,T)
Form: Clear Liquid
Boiling point (°C): 164
Specific Gravity (20/20): 0.94
Specific rotation [a]20/D: 19.5 deg (C=10, EtOH)
Storage Temperature: 0-10°C
Catalog Number: TCM1107-001G
Supplier: TCI America



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Description:   MF=C13H15No4 MW=249.27 500Mg
Catalog Number: 101934-336
Supplier: Matrix Scientific



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Description:   4-Pyrrolidin-1-ylpyridine-2-carbaldehyde ≥97%
Catalog Number: 102835-422
Supplier: Matrix Scientific



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Description:   1-(4-Bromo-2-trifluoromethylphenyl)pyrrolidine ≥97%
Catalog Number: 77383-942
Supplier: AOB CHEM USA



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Description:   Matrix Scientific Part Number: 021670-500MG , MDL Number: MFCD02663452
Catalog Number: 101812-518
Supplier: Matrix Scientific



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Description:   Matrix Scientific Part Number: 053648-500MG , MDL Number: MFCD13562879
Catalog Number: 101904-480
Supplier: Matrix Scientific



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Description:   5-(4-Bromophenyl)pyrrolidin-2-one, Purity: 96%, CAS Number: 207989-90-0, Appearance: Solid, Storage: Sealed in dry, Room Temperature, Size: 250MG
Catalog Number: 76823-542
Supplier: AMBEED, INC



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