| Weight | 94.545 g/mol |
|---|---|
| Formula | C2H7ClN2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Acetamidine hydrochloride (124-42-5)
acetamidine · acetamidine sulfate (1:1) · acetamidine monoacetate
Score:
#59 in Medicinal chemistry
,
#7201 in Chemistry
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- Suppression of acute experimental colitis by a highly selective inducible nitric-oxide synthase inhibitor, N-[3-(aminomethyl)benzyl]acetamidine (Journal of Pharmacology and Experimental Therapeutics, 2001)
- Inhibition of inducible nitric oxide synthase by acetamidine derivatives of hetero-substituted lysine and homolysine (Bioorganic & Medicinal Chemistry Letters, 2000)
- N-(3-(aminomethyl)benzyl)acetamidine, an inducible nitric oxide synthase inhibitor, decreases colonic inflammation induced by trinitrobenzene sulphonic acid in rats. (Life Sciences, 2001)
- Protective effect of N-(3-(aminomethyl)benzyl) acetamidine, an inducible nitric oxide synthase inhibitor, in brain slices exposed to oxygen-glucose deprivation. (European Journal of Pharmacology, 1998)
- The crystal structure of diammine bis(acetamidine)platinum(II) chloride monohydrate, Pt(NH3)2[CH3.C.(NH2).NH]2Cl2.H2O (Journal of Inorganic and Nuclear Chemistry, 1962)
- A Convenient Synthesis of Formamidine and Acetamidine Acetate (Journal of the American Chemical Society, 1960)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - acetamidine
- acetamidine sulfate (1:1)
- acetamidine monoacetate
- acetamidine monohydrochloride
- acetamidinium
-
SMILESCC(=N)N.Cl
-
InChIKeyWCQOBLXWLRDEQA-UHFFFAOYSA-N
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