InChI key
OKGXJRGLYVRVNE-UHFFFAOYSA-N
InChI
1S/C2H6N4S/c3-1(4)6-2(5)7/h(H6,3,4,5,6,7)
SMILES string
NC(=N)NC(N)=S
assay
99%
mp
171-173 °C (lit.)
functional group
amine, thiourea
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
I N Petrin et al.
Voprosy meditsinskoi khimii, 39(6), 36-39 (1993-11-01)
Exotoxic shock was simulated in non-linear rat males anesthetized with barbital after intragastric administration of 70% acetic acid at a dose of 4 ml/kg using a gastric tube. Energy metabolism and the rate of lipid peroxidation were studied in heart
I G Vlasova et al.
Farmakologiia i toksikologiia, 52(1), 12-16 (1989-01-01)
The effects of some antihypoxants (piracetam, GABA, sodium hydroxybutyrate and gutimine) on the electrical activity of the cerebellar neurons (Purkinje cells) of rats and mice were studied in the surviving slices under normoxia and increasing hypoxia. All the agents were
V V Morrison
Anesteziologiia i reanimatologiia, (5)(5), 27-29 (1995-09-01)
Levels of sodium and potassium ions in muscle tissue, blood plasma and red cells were measured, and the index characterizing the capacity of tissue to accumulate cations from the environment and the discrimination coefficient were calculated in experiments on white
V D Luk'ianchuk et al.
Eksperimental'naia i klinicheskaia farmakologiia, 61(4), 72-79 (1998-10-23)
The survey deals with the up-to-date information in the literature on the problem of pharmacological correction of pathological changes found in the organism in the hypoxic syndrome. The principal approaches to pharmacotherapy of this pathological condition are pointed out. Information
Royce A Wilkinson et al.
Antimicrobial agents and chemotherapy, 55(1), 255-263 (2010-10-13)
The G-protein-coupled receptor CXCR4 acts as a coreceptor for human immunodeficiency virus type 1 (HIV-1) infection, as well as being involved in signaling cell migration and proliferation. Compounds that block CXCR4 interactions have potential uses as HIV entry inhibitors to
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