N-[Amino(imino)methyl]morpholine-4-carboximidamide hydrochloride

CAS : 3731-59-7

Ref. 3D-FA119412

Informations sur le produit

• Nom: N-[Amino(imino)methyl]morpholine-4-carboximidamide hydrochloride
• Synonymes: 4-morpholinecarboximidamide, N-(aminoiminomethyl)-, hydrochloride, 1-(1-Morpholinoformimidoyl)Guanidine, 4-Morpholinecarboxamidine, N-amidino-, 4-Morpholinecarboximidamide, N-(aminoiminomethyl)-, 4-Morpholinecarboximidoylguanidine, Guanidine, 4-morpholinecarboximidoyl-, Jd 1022, N-(Aminoiminomethyl)-4-morpholinecarboximidamide, N-[Imino(4-morpholinyl)methyl]guanidine, N-carbamimidoylmorpholine-4-carboximidamide, N¹,N¹-Anhydrobis(β-hydroxyethyl)biguanide, Skf 8898A, Vironil, Virugon, Virumin, Wirumin

Description

N-[Amino(imino)methyl]morpholine-4-carboximidamide hydrochloride (AMMC) is an antimicrobial agent that inhibits protein synthesis by binding to the 30S ribosomal subunit. AMMC has been shown to be effective against a number of viruses, including HIV, herpes simplex virus type 1 and 2, influenza A and B, and respiratory syncytial virus. AMMC also inhibits the growth of bacteria that are resistant to other antibiotics such as tetracyclines, chloramphenicol, erythromycin, penicillin, sulfonamides and trimethoprim. AMMC has been shown to inhibit the proliferation of cells in bowel disease models with pharmacological agents. This drug is also used for the rapid detection of microorganisms in biological samples by its ability to bind to RNA polymerase or DNA polymerase enzyme activities.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 171.2 g/mol
• Formule: C₆H₁₃N₅O
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C6H13N5O/c7-5(8)10-6(9)11-1-3-12-4-2-11/h1-4H2,(H5,7,8,9,10)
• Code InChI: InChIKey=KJHOZAZQWVKILO-UHFFFAOYSA-N
• SMILES: N=C(N=C(N)N)N1CCOCC1