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Detail of "3310-41-6"

  • CAS Number:
  • 3310-41-6
  • Name:
  • 2(1H)-Pyrimidinone,6-hydrazinyl-

  • Superlist Name:
  • 2-Hydroxy-4-hydrazinopyrimidine
  • Molecular Structure:
  • Formula:
  • C4H6N4O
  • Molecular Weight:
  • 126.12
  • Synonyms:
  • 2(1H)-Pyrimidinone,4-hydrazino- (6CI,7CI,8CI);2,4(1H,3H)-Pyrimidinedione, 4-hydrazone (9CI);4-(Hydrazino)pyrimidin-2(1H)-one;N4-Aminocytosine;
  • Density:
  • 1.558 g/cm3
  • Boiling Point:
  • 515.242 °C at 760 mmHg
  • Flash Point:
  • 265.409 °C

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:RennoTech Co., Ltd. [ China (Mainland)]

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Address:23 Lijing Road, Nanjing Hi-Tech Zone, Nanjing, Jiangsu, China, 210061

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:Beilstein (Wuhan) Science & Technology Co ., Ltd. [ China (Mainland)]

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Tel:86-27-82315360

Address:17 Gutain 5 Road, Suite 311 , Qiaokou district, Wuhan, China

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:Nanjing Puruida Pharmaceutical Technology Co., Ltd. [ China (Mainland)]

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Address:RM301 Section A Bio-Pharm. Building, Venture Center of Nanjing High-tech Development Zone,

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:Achemo Sientific cooperation [ Hong Kong]

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Address:38 Plaza,38 Shantung street,MongKoK,kowloon,Hongkong

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:Win-Win chemical Co.Ltd [ China (Mainland)]

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Address:Wenzhou china

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CAS No.3310-41-6 2-Hydroxy-4-hydrazinopyrimidine

Supplier:LianYunGang Henrychem Science Co.,Ltd. [ China (Mainland)]

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Address:No.23, Haining Road, Xinpu Area, Lianyungang, Jiangsu, 222000, P.R. China

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Reference

Mutagenicity of N4-aminocytidine and its derivatives in Chinese hamster lung V-79 cells
Mutagenicity of N4-aminocytidine and its derivatives in Chinese hamster lung V-79 cells. Incorporation of N4-aminocytosine into cellular DNA. Nomura, Akinori; Negishi, Kazuo; Hayatsu, Hikoya; Kuroda, Yukiaki (Fac. Pharm. Sci., Okayama Univ., Okayama 700, Japan). Mutat. Res., 177(2), 283-7 (English) 1987. CODEN: MUREAV. ISSN: 0027-5107. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) N4-Aminocytidine (I) [57294-74-3] induced mutation to 6-thioguanine [154-42-7] resistance in Chinese hamster lung V-79 cells in culture. Previous studies with exptl. systems of in vitro DNA synthesis and of phage and bacterial mutagenesis have shown that this nucleoside analog induced base-pair transitions through its incorporation into DNA, with its erroneous base-pairing property. Incorporation of exogenously added [5-3H]N4-aminocytidine into the DNA of V-79 cells was obsd. in the present study. N4-Aminodeoxycytidine [52725-05-0] was not mutagenic for the V-79 cells. Several alkylated N4-aminocytidine derivs. were tested for their mutagenicity in this system. Those with an alkyl group on the N'-nitrogen of the hydrazino group at position 4 of N4-aminocytidine were mutagenic, but those having an alkyl on the N4-nitrogen were not. These results are consistent with those previously obsd. in the bacterial mutagenesis systems, and agree with a mechanism of mutation in which a tautomerization of N4-aminocytosine [3310-41-6] is the necessary step for causing the erroneous base pairing.Except for chemicals metioned above, 52725-05-0 and 3310-41-6 are also used. .
Proofreading of a mutagenic nucleotide, N4-aminodeoxycytidylic acid, by Escherichia coli DNA polymerase I
Proofreading of a mutagenic nucleotide, N4-aminodeoxycytidylic acid, by Escherichia coli DNA polymerase I. Takahashi, Mitsuko; Negishi, Kazuo; Hayatsu, Hikoya (Fac. Pharm. Sci., Okayama Univ., Okayama 700, Japan). Biochem. Biophys. Res. Commun., 143(1), 104-9 (English) 1987. CODEN: BBRCA9. ISSN: 0006-291X. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Genetics) N4-aminodeoxycytidine triphosphate [90335-46-9], a putative metabolite of N4-aminocytidine [52725-05-0] which is a potent mutagen, is incorporated in vitro into polynucleotides in place of dCTP and at a much lesser extent, but significantly, in place of dTTP by the E. coli DNA polymerase I [9012-90-2] large fragment. The activity of the polymerase to proofread this unnatural nucleotide was investigated. The 3'-5' exonuclease [79393-91-2] in the polymerase recognizes N4-aminocytosine [3310-41-6] as an incorrect base when N4-aminocytosine is incorporated opposite adenine, but the enzyme cannot distinguish N4-aminocytosine from cytosine when it is incorporated opposite guanine.Except for chemicals metioned above, 3310-41-6 and 79393-91-2 are also used. .
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