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Home Sulfos L-Buthionine-(s,r)-sulfoximine

L-Buthionine-(s,r)-sulfoximine

CAS No.:
83730-53-4
Catalog Number:
AG00IDBJ
Molecular Formula:
C8H18N2O3S
Molecular Weight:
222.3051
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
≥98%
1 week
United States
$147
- +
500mg
≥98%
1 week
United States
$229
- +
1g
≥98%
1 week
United States
$382
- +
Product Description
Catalog Number:
AG00IDBJ
Chemical Name:
L-Buthionine-(s,r)-sulfoximine
CAS Number:
83730-53-4
Molecular Formula:
C8H18N2O3S
Molecular Weight:
222.3051
MDL Number:
MFCD00067000
IUPAC Name:
(2S)-2-amino-4-(butylsulfonimidoyl)butanoic acid
InChI:
InChI=1S/C8H18N2O3S/c1-2-3-5-14(10,13)6-4-7(9)8(11)12/h7,10H,2-6,9H2,1H3,(H,11,12)/t7-,14?/m0/s1
InChI Key:
KJQFBVYMGADDTQ-CVSPRKDYSA-N
SMILES:
CCCCS(=O)(=N)CC[C@@H](C(=O)O)N
NSC Number:
326231
Properties
Complexity:
284  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
222.104g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
222.303g/mol
Monoisotopic Mass:
222.104g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
113A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.6  
Literature
Title Journal
Collateral sensitivity of multidrug-resistant cells to the orphan drug tiopronin. Journal of medicinal chemistry 20110728
Extracellular redox modulation by regulatory T cells. Nature chemical biology 20091001
Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum. Nature chemical biology 20091001
Protein S-guanylation by the biological signal 8-nitroguanosine 3',5'-cyclic monophosphate. Nature chemical biology 20071101
Targeting thioredoxin reductase is a basis for cancer therapy by arsenic trioxide. Proceedings of the National Academy of Sciences of the United States of America 20070724
Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells. The Journal of biological chemistry 20020419
Properties