P1101
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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线性分子式:
[-SC(CH3)2CH(NH2)CO2H]2
化学文摘社编号:
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
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
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
Fabrizio Apruzzese et al.
Annali di chimica, 94(1-2), 45-56 (2004-05-15)
D-penicillamine disulfide (PNS) shows protolytic properties and is able to form complexes with cations, because it has two aminic groups and two carboxylic groups. The four protonation constants of its deprotonated species were determined by means of electromotive force (e.m.f.)
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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