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Merck
CN

P1101

Sigma-Aldrich

D-青霉胺二硫化物

97%, cell analysis

别名:

3,3′-二硫代双(2-氨基-3-甲基丁酸), S,S′-二(D-青霉胺), 二硫青霉胺

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About This Item

线性分子式:
[-SC(CH3)2CH(NH2)CO2H]2
CAS号:
分子量:
296.41
Beilstein:
4461521
EC 号:
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.22

产品名称

D-青霉胺二硫化物, 97%

质量水平

方案

97%

表单

powder or crystals

旋光性

[α]25/D −75°, c = 1 in 1 M NaOH

反应适用性

reaction type: solution phase peptide synthesis

颜色

white

mp

204 °C (dec.) (lit.)

应用

cell analysis

SMILES字符串

CC(C)(SSC(C)(C)[C@@H](N)C(O)=O)[C@@H](N)C(O)=O

InChI

1S/C10H20N2O4S2/c1-9(2,5(11)7(13)14)17-18-10(3,4)6(12)8(15)16/h5-6H,11-12H2,1-4H3,(H,13,14)(H,15,16)/t5-,6-/m0/s1

InChI key

POYPKGFSZHXASD-WDSKDSINSA-N

应用

Used in pharmacological studies of:
  • Molecules dermatomyositis activity
  • Antimelanoma activity of apoptogenic carbonyl scavengers

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Determination of penicillamine in encapsulated formulations by high-performance liquid chromatography.
S Biffar et al.
Journal of chromatography, 318(2), 404-407 (1985-01-18)
G T Yamashita et al.
Journal of chromatography, 491(2), 341-354 (1989-07-21)
Methodology is described for the simultaneous determination of D-penicillamine, penicillamine disulfide and the penicillamine-glutathione mixed disulfide, as well as glutathione and glutathione disulfide, in human plasma, erythrocytes and urine. The various thiols and disulfides are separated by reversed-phase ion-pairing liquid
Anshul Gupte et al.
Journal of inorganic biochemistry, 101(4), 594-602 (2007-02-06)
D-Penicillamine is a potent copper (Cu) chelating agent. D-Pen reduces Cu(II) to Cu(I) in the process of chelation while at the same time being oxidized to D-penicillamine disulfide. It has been proposed that hydrogen peroxide is generated during this process.
Amit K Galande et al.
Biopolymers, 71(5), 534-551 (2003-11-25)
A recently rediscovered reaction of base-assisted lanthionine formation has been applied to several systems of disulfide-bridged peptides. In addition to previously described nonapeptides consisting of i, i+3 cystine linkages, the reaction has now been extended to systems consisting of shorter
[Determination of D-penicillamine and its metabolites in blood and urine].
K Kyogoku et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 102(4), 322-327 (1982-04-01)

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