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Merck
CN

CBR00275

Sigma-Aldrich

5-氨基-5-氧戊酸

AldrichCPR

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经验公式(希尔记法):
C5H9NO3
CAS号:
分子量:
131.13
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:

形式

solid

SMILES字符串

O=C(CCCC(O)=O)N

InChI

1S/C5H9NO3/c6-4(7)2-1-3-5(8)9/h1-3H2,(H2,6,7)(H,8,9)

InChI key

GTFMAONWNTUZEW-UHFFFAOYSA-N

其他说明

Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.

NOTWITHSTANDING ANY CONTRARY PROVISION CONTAINED IN SIGMA-ALDRICH′S STANDARD TERMS AND CONDITIONS OF SALE OR AN AGREEMENT BETWEEN SIGMA-ALDRICH AND BUYER, SIGMA-ALDRICH SELLS THIS PRODUCT "AS-IS" AND MAKES NO REPRESENTATION OR WARRANTY WHATSOEVER WITH RESPECT TO THIS PRODUCT, INCLUDING ANY (A) WARRANTY OF MERCHANTABILITY; (B) WARRANTY OF FITNESS FOR A PARTICULAR PURPOSE; OR (C) WARRANTY AGAINST INFRINGEMENT OF INTELLECTUAL PROPERTY RIGHTS OF A THIRD PARTY; WHETHER ARISING BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE.

法律信息

Product of ChemBridge Corp.

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Eye Irrit. 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Cholecystokinin receptor antagonists.
K A Zucker et al.
The Journal of surgical research, 45(5), 496-504 (1988-11-01)
T Takács et al.
International journal of pancreatology : official journal of the International Association of Pancreatology, 10(1), 1-8 (1991-09-01)
In this article, the effects of different classes of cholecystokinin (CCK) receptor antagonists in CCK-related physiological processes of the pancreas have been discussed. Both glutaramic acid derivatives and natural (benzodiazepine) analogs are potent, competitive antagonists of peripheral CCK receptors. These
D J Goon et al.
Bioconjugate chemistry, 5(5), 418-422 (1994-09-01)
By use of a glutaramyl-beta-alanyl spacer group, a hapten for the polychlorinated biphenyl, 2,2',4,4',5,5'-hexachlorobiphenyl (1), viz., 2-amino-2',4,4',5,5'-pentachlorobiphenyl (2), was successfully conjugated to carrier proteins to provide immunogens with high hapten/protein molar substitution ratios (MSR's). The procedure allows for the incorporation

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