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Merck
CN

C6760

Cytosine β-D-arabinofuranoside 5′-monophosphate

≥99%

别名:

Ara-CMP

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关于此项目

经验公式(希尔记法):
C9H14N3O8P
化学文摘社编号:
分子量:
323.20
UNSPSC Code:
41106305
PubChem Substance ID:
MDL number:
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assay

≥99%

form

solid

storage temp.

−20°C

SMILES string

NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]2O

InChI

1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7+,8-/m1/s1

InChI key

IERHLVCPSMICTF-CCXZUQQUSA-N



pictograms

Health hazard

signalword

Warning

hcodes

pcodes

Hazard Classifications

Carc. 2

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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D D Ross et al.
Cancer research, 50(9), 2658-2666 (1990-05-01)
The pH-step alkaline elution method enables the isolation and quantification of nascent DNA (nDNA) replication intermediates, including Okazaki fragments, short length nDNA from replicon origins, longer lengths of nascent but subgenomic length nDNA (molecular weight, 20-30 x 10(6)), and full
E M McIntosh et al.
Current genetics, 10(8), 579-585 (1986-01-01)
Cytosine arabinoside (araC), a potent inhibitor of DNA replication in mammalian cells, was found to be completely ineffective in Saccharomyces cerevisiae. The 5' monophosphate derivative, araCMP, is toxic and effectively inhibits both nuclear and mitochondrial DNA synthesis in this organism.
Human deoxycytidylate deaminase. Substrate and regulator specificities and their chemotherapeutic implications.
W R Mancini et al.
Molecular pharmacology, 23(1), 159-164 (1983-01-01)