Dacisteine structure
|
Common Name | Dacisteine | ||
---|---|---|---|---|
CAS Number | 18725-37-6 | Molecular Weight | 205.23200 | |
Density | 1.314g/cm3 | Boiling Point | 446.8ºC at 760 mmHg | |
Molecular Formula | C7H11NO4S | Melting Point | 114-116°C | |
MSDS | N/A | Flash Point | 224ºC |
Use of DacisteineDacisteine (N,S-Diacetyl-L-cysteine) is a cysteine derivative and displays a less New Delhi metallo-beta-lactamase-1 (NDM-1) inhibitor with an IC50 value of 1000 μM[1]. Dacisteine can be used for the treatment of cardiovascular and cerebrovascular diseases caused by platelet aggregation[2]. |
Name | (2R)-2-acetamido-3-acetylsulfanylpropanoic acid |
---|---|
Synonym | More Synonyms |
Description | Dacisteine (N,S-Diacetyl-L-cysteine) is a cysteine derivative and displays a less New Delhi metallo-beta-lactamase-1 (NDM-1) inhibitor with an IC50 value of 1000 μM[1]. Dacisteine can be used for the treatment of cardiovascular and cerebrovascular diseases caused by platelet aggregation[2]. |
---|---|
Related Catalog | |
Target |
IC50: 1000 μM (NDM-1)[1] |
In Vivo | Dacisteine is a preparing agent for treating or preventing cardiovascular and cerebrovascular diseases caused by platelet aggregation. |
References |
Density | 1.314g/cm3 |
---|---|
Boiling Point | 446.8ºC at 760 mmHg |
Melting Point | 114-116°C |
Molecular Formula | C7H11NO4S |
Molecular Weight | 205.23200 |
Flash Point | 224ºC |
Exact Mass | 205.04100 |
PSA | 108.77000 |
LogP | 0.24630 |
Vapour Pressure | 3.13E-09mmHg at 25°C |
Index of Refraction | 1.522 |
Storage condition | Refrigerator |
HS Code | 2930909090 |
---|
~81% Dacisteine CAS#:18725-37-6 |
Literature: Pharmazie, , vol. 49, # 4 p. 249 - 252 |
~% Dacisteine CAS#:18725-37-6 |
Literature: Farmaco, Edizione Scientifica, , vol. 31, # 11 p. 767 - 775 |
~% Dacisteine CAS#:18725-37-6 |
Literature: Biochemical Journal, , vol. 57, p. 360,363 |
HS Code | 2930909090 |
---|---|
Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Formation of the thioester, N,S-diacetylcysteine, from acetaldehyde and N,N'diacetylcystine in aqueous solution with ultraviolet light.
J. Mol. Evol. 17(2) , 103-7, (1981) The thioester, N,S-diacetylcysteine, is formed during the illumination of phosphate buffered (pH 7.0) aqueous solutions of acetaldehyde and N,N'-diacetylcystine with ultraviolet light. The yield of N,... |
Dacisteina |
Dacisteine |
S,N-diacetylcysteine |
N,S-Diacetyl |
Acetylcysteine impurity D |
N,S-diacetyl-D,L-cysteine |
N,S-diacetyl-L-cysteine |
N,S-Diacetylcysteine |
Dacisteinum |
N,S-diacetil-L-cisteina |