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NSC 65346

更新时间:2025-08-25 23:56:32

NSC 65346结构式
NSC 65346结构式
品牌特惠专场
常用名 NSC 65346 英文名 Sangivamycin
CAS号 18417-89-5 分子量 309.28
密度 N/A 沸点 880.6ºC at 760 mmHg
分子式 C12H15N5O5 熔点 N/A
MSDS 中文版 美版 闪点 486.4ºC
符号 GHS06
GHS06
信号词 Danger

 NSC 65346用途


Sangivamycin(NSC 65346)是一种核苷类似物,是一种Ki为10μM的蛋白激酶C(PKC)的有效抑制剂。Sangivamycin对多种人类癌症具有有效的抗增殖活性[1][2]。

 NSC 65346名称

中文名 桑霉素
英文名 sangivamycin
中文别名 桑吉瓦霉素
英文别名 更多

 NSC 65346生物活性

描述 Sangivamycin(NSC 65346)是一种核苷类似物,是一种Ki为10μM的蛋白激酶C(PKC)的有效抑制剂。Sangivamycin对多种人类癌症具有有效的抗增殖活性[1][2]。
相关类别
体外研究 Sangivamycin对药物敏感的MCF7/野生型(WT)细胞和对多药耐药的MCF7/阿霉素耐药(ADR)人乳腺癌细胞具有不同的抗肿瘤作用,导致细胞大量凋亡[2]。Sangivamycin(0.3μM;0-72小时)显示出几乎最大的细胞杀伤作用(对于MCF7/ADR)或细胞抑制作用(对于MCF7/WT)[2]。桑格霉素激活MCF7/ADR细胞中的半胱天冬酶。当MCF7/ADR细胞暴露于桑格霉素(0.3μM;)时,48小时内检测到大量层粘连蛋白a裂解为28 kDa片段[2]。
参考文献

[1]. Loomis CR, Bell RM. Sangivamycin, a nucleoside analogue, is a potent inhibitor of protein kinase C. J Biol Chem. 1988;263(4):1682-1692.

[2]. Lee SA, et al. The nucleoside analog sangivamycin induces apoptotic cell death in breast carcinoma MCF7/adriamycin-resistant cells via protein kinase Cdelta and JNK activation. J Biol Chem. 2007;282(20):15271-15283.

 NSC 65346物理化学性质

沸点 880.6ºC at 760 mmHg
分子式 C12H15N5O5
分子量 309.28
闪点 486.4ºC
精确质量 327.11800
PSA 178.97000
InChIKey OBZJZDHRXBKKTJ-JTFADIMSSA-N
SMILES NC(=O)c1cn(C2OC(CO)C(O)C2O)c2ncnc(N)c12
外观性状 固体
蒸汽压 3.3E-33mmHg at 25°C
储存条件 2-8°C,密封,干燥

 NSC 65346毒性和生态

 NSC 65346安全信息

符号 GHS06
GHS06
信号词 Danger
危害声明 H300-H310-H330
警示性声明 P260-P264-P280-P284-P302 + P350-P310
个人防护装备 Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
危害码 (欧洲) T+
风险声明 (欧洲) 26/27/28
危险品运输编码 UN 2811 6.1/PG 2
RTECS号 UY9355000

 NSC 65346上下游产品

NSC 65346上游产品  0

NSC 65346下游产品  1

 NSC 65346文献28

更多文献
Synthesis and in vitro antitumor activity of some amino-deoxy 7-hexofuranosylpyrrolo[2,3-d]pyrimidines.

Carbohydr. Res. 308(3-4) , 319-28, (1998)

7-(6-amino-6-deoxy-beta-D-glucofuranosyl)-5-cyanopyrrolo[2,3 -d]pyrimidine (22) and 7-(3-amino-methyl-3-deoxy-beta-D-allofuranosyl)-5- cyanopyrrolo[2,3-d]pyrimidine (28) were synthesized by sequential...

Kinetics and localization of the phosphorylation of rhodopsin by protein kinase C.

J. Biol. Chem. 270(12) , 6710-7, (1995)

Protein kinase C isolated from retina catalyzes the stoichiometric phosphorylation of bovine rhodopsin. Enzymological studies using receptor in rod outer segment membranes stripped of peripheral prote...

Synthesis of pyrrolo[2,1-f][1,2,4]triazine C-nucleosides. Isosteres of sangivamycin, tubercidin, and toyocamycin.

Carbohydr. Res. 331(1) , 77-82, (2001)

Syntheses of pyrrolo[2,1-f][1,2,4]triazine C-nucleosides are reported. Treatment of pyranulose glycoside with aminoguanidine in acetic acid gave the corresponding semicarbazone in 96% yield. The ring ...

 NSC 65346靶点实验

查看更多实验

实验名称:Increase in Bax levels in human multidrug resistant MCF/ADR cells at 0.3 uM by immuno...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945619
实验名称:Increase in Bcl-2 levels in human multidrug resistant MCF/ADR cells at 0.3 uM by immu...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945618
实验名称:Induction of apoptosis in human drug-sensitive MCF/WT cells assessed as cleavage of l...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945621
实验名称:Induction of apoptosis in human multidrug resistant MCF/ADR cells assessed as cleavag...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945620
实验名称:Minimum inhibitory concentration required to reduce reo virus type 1 induced cytopath...
来源:ChEMBL
靶标:Mammalian orthoreovirus 1
External Id:CHEMBL799910
实验名称:Increase in Bcl-x/s levels in human drug-sensitive MCF/WT cells at 0.3 uM by immunobl...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945615
实验名称:Increase in Bcl-x/l levels in human multidrug resistant MCF/ADR cells at 0.3 uM by im...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL942530
实验名称:Increase in Bcl-2 levels in human drug-sensitive MCF/WT cells at 0.3 uM by immunoblot...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945617
实验名称:Increase in Bcl-x/s levels in human multidrug resistant MCF/ADR cells at 0.3 uM by im...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL945616
实验名称:Induction of c-Jun phosphorylation in human drug-sensitive MCF/WT cells at 0.3 uM
来源:ChEMBL
靶标:Transcription factor Jun
External Id:CHEMBL950785
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 NSC 65346英文别名

7-Carboxamido-7-deazaadenosine
7-DEAZA-7-CARBAMOYLADENOSINE
7-DEAZAADENOSINE-7-CARBOXAMIDE
SANGIVAMYCIN
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