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About This Item
Empirical Formula (Hill Notation):
C3H6N2S
CAS Number:
Molecular Weight:
102.16
EC Number:
217-224-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
105367
MDL number:
InChI
1S/C3H6N2S/c4-3-5-1-2-6-3/h1-2H2,(H2,4,5)
InChI key
REGFWZVTTFGQOJ-UHFFFAOYSA-N
SMILES string
NC1=NCCS1
assay
97%
mp
79-82 °C (lit.)
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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J J Díaz Gil et al.
Revista espanola de oncologia, 29(4), 615-621 (1982-01-01)
Some aspects of the effect of thioproline and 2-amino-thiazoline-HCl on HeLa cell cultures are studied. Both drugs, at 1 mM concentrations, produce morphological changes that become stabilized after four days. The morphology changes depend on the microtubules, microfilaments, and de
Reverse transformation agent and their ability to complex metal ions.
Z X Huang et al.
European journal of cancer & clinical oncology, 17(10), 1151-1152 (1981-10-01)
M J Pine et al.
Journal of medicine, 14(5-6), 433-449 (1983-01-01)
2--amino-2-thiazoline (AT) and 1-thiazolidine-4-carboxylate (TC, thioproline), which have been previously proposed as agents of reverse transformation, have been examined as antitumor agents in several rodent tumor systems. AT administration reduced tumor incidence in sym-dimethylhydrazine treated outbred ICR Swiss female mice
[Mechanisms of the radioprotective effect of 2-amino-2-thiazoline in experiments on yeasts].
L T Zolotareva
Radiobiologiia, 22(2), 257-258 (1982-03-01)
Preliminary clinical results with norgamem (thioproline) and revercan (2-amino-2-thiazoline): the first inducers of reverse transformation.
A Brugarolas et al.
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer, 80, 346-350 (1982-01-01)
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