10212-25-6 | Cyclocytidine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$18.00	$12.00
1g	95%	in stock	$25.00	$17.00
5g	95%	in stock	$30.00	$21.00
25g	95%	in stock	$106.00	$74.00
100g	95%	in stock	$339.00	$237.00

Description

• Catalog Number: AI05590
• Chemical Name: Cyclocytidine hydrochloride
• CAS Number: 10212-25-6
• Molecular Formula: C9H12ClN3O4
• Molecular Weight: 261.6623
• MDL Number: MFCD00012636
• SMILES: OC[C@H]1O[C@@H]2[C@H]([C@@H]1O)Oc1n2ccc(=N)n1.Cl

Computed Properties

• Complexity: 394
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 4
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 4
• Rotatable Bond Count: 1

Upstream Synthesis Route

Ancitabine Hydrochloride is a potent chemical compound widely utilized in the field of chemical synthesis. As a versatile nucleoside analog, it serves as a crucial building block in the creation of various pharmaceuticals, specifically antiviral and anticancer drugs. By incorporating Ancitabine Hydrochloride into synthesis processes, chemists can modify and enhance the properties of the final products, leading to more effective and targeted treatment options. Its unique structure and reactivity make it an indispensable tool in the realm of medicinal chemistry, enabling the development of novel compounds with improved therapeutic potentials. In chemical synthesis, Ancitabine Hydrochloride plays a vital role in driving innovation and progress towards the creation of breakthrough medications.

Literature

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Ultrastructural histochemical studies of secretory granule replenishment in rat submandibular granular tubules after cyclocytidine-induced secretion.

  Journal of submicroscopic cytology and pathology 20020701

• 1-(2,3-Anhydro-beta-D-lyxofuranosyl)cytosine derivatives as potential inhibitors of the human immunodeficiency virus.

  Journal of medicinal chemistry 19880701

• Effects of 2,2'-O-cyclocytidine and acyclovir on latent herpes simplex virus in trigeminal ganglia of mice.

  Antimicrobial agents and chemotherapy 19860201

• Antiviral activities of acyl derivatives of 2,2'-anhydro-1-beta-D-arabinofuranosylcytosine and 1-beta-D-arabinofuranosylcytosine in cell culture.

  Antimicrobial agents and chemotherapy 19770201