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Home Other Building Blocks D-Penicillamine disulfide

D-Penicillamine disulfide

CAS No.:
20902-45-8
Catalog Number:
AG003PW6
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG003PW6
Chemical Name:
D-Penicillamine disulfide
CAS Number:
20902-45-8
MDL Number:
MFCD00004264
IUPAC Name:
(2S)-2-amino-3-[[(1S)-1-amino-1-carboxy-2-methylpropan-2-yl]disulfanyl]-3-methylbutanoic acid
InChI:
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
EC Number:
244-107-2
UNII:
Q98FPI4N5P
Properties
Complexity:
302  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
296.086g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0
Molecular Weight:
296.4g/mol
Monoisotopic Mass:
296.086g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
177A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-5  
Literature
Title Journal
An investigation into copper catalyzed D-penicillamine oxidation and subsequent hydrogen peroxide generation. Journal of inorganic biochemistry 20070401
Penicillamine disulfide (PNS) and alkaline cations. Annali di chimica 20040101
Understanding base-assisted desulfurization using a variety of disulfide-bridged peptides. Biopolymers 20030101
Studies on the mechanism of the formation of the penicillin antigen. I. Delayed allergic cross-reactions among penicillin G and its degradation products. The Journal of experimental medicine 19601130
Properties