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Merck
CN

444170-M

Manumycin A, Streptomyces parvulus

An antibiotic with antitumor properties.

别名:

Manumycin A, Streptomyces parvulus

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关于此项目

经验公式(希尔记法):
C31H38N2O7
化学文摘社编号:
分子量:
550.64
UNSPSC Code:
12352200
MDL number:
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InChI

1S/C31H38N2O7/c1-5-6-11-19(2)16-20(3)17-21(4)30(38)32-22-18-31(39,29-28(40-29)27(22)37)15-10-8-7-9-12-25(36)33-26-23(34)13-14-24(26)35/h7-10,12,15-19,28-29,34,39H,5-6,11,13-14H2,1-4H3,(H,32,38)(H,33,36)/b8-7+,12-9+,15-10+,20-16+,21-17+/t19-,28-,29-,31+/m1/s1

InChI key

TWWQHCKLTXDWBD-MVTGTTCWSA-N

assay

≥96% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

yellow to brown

solubility

DMSO: 10 mg/mL, chloroform: soluble, methanol: soluble

General description

An antibiotic with antitumor properties. A cell-permeable potent and selective inhibitor of farnesyltransferase (FTase; IC50 = 5 µM) compared to geranylgeranyltransferase I (GGTase I; IC50 = 180 µM). Manumycin acts as a competitive inhibitor of FTase with respect to farnesylpyrophosphate (FPP; Ki = 1.2 µM), but acts as a noncompetitive inhibitor with respect to the Ras acceptor protein. Reported to inhibit the growth and invasive activity of pancreatic cancer cells.

Biochem/physiol Actions

Primary Target
Farnesyltransferase (FTAse)
Target IC50: 5 µM against farnesyltransferase (FTase); 180 µM against geranylgeranyltransferase I (GGTase I)

Preparation Note

Following reconstitution, aliquot and freeze (-20°C).

Other Notes

Kainuma, O., et al. 1997. Pancreas15, 379.
Nagase, T., et al. 1996. Int. J. Cancer 65, 620.
Hara, M., et al. 1995. Proc. Natl. Acad. Sci. USA92, 3333.
Hara, M., et al. 1993. Proc. Natl. Acad. Sci. USA90, 2281.
Tamanoi, R. 1993. Trends Biochem. Sci.18, 349.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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