9H-Purin-6-amine, 9-β-D-arabinofuranosyl-, hydrate (1:1)
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9H-Purin-6-amine, 9-β-D-arabinofuranosyl-, hydrate (1:1)
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CAS No:
24356-66-9
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Formula:
C10H13N5O4.H2O
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Chemical Name:
9H-Purin-6-amine, 9-β-D-arabinofuranosyl-, hydrate (1:1)
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Synonyms:
9H-Purin-6-amine,9-β-D-arabinofuranosyl-,hydrate (1:1);Adenine,9-β-D-arabinofuranosyl-,monohydrate;9H-Purin-6-amine,9-β-D-arabinofuranosyl-,monohydrate;Adenine arabinofuranoside hydrate;Vidarabine monohydrate
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CAS No:
Description
Vidarabine monohydrate is an adenine arabinoside.|Vidarabine is a nucleoside analog with activity against herpes simplex virus and varicella zoster virus. Vidarabine is converted to a monophosphate by viral thymidine kinase and is further modified to a triphosphate form by host enzymes. Vidarabine triphosphate directly inhibits DNA polymerase and also acts as a chain terminator in DNA replication.|A nucleoside antibiotic isolated from Streptomyces antibioticus. It has some antineoplastic properties and has broad spectrum activity against DNA viruses in cell cultures and significant antiviral activity against infections caused by a variety of viruses such as the herpes viruses, the VACCINIA VIRUS and varicella zoster virus.
9H-Purin-6-amine, 9-β-D-arabinofuranosyl-, hydrate (1:1) Basic Attributes
285.2566
285.10731860 g/mol
678-339-4
FA2DM6879K
C929
Characteristics
141 Ų
1.3439
253 °C
427.69°C (rough estimate)
-3.0 ° (C=1, DMF)
513.5mg/L(temperature not stated)
Safety Information
62
45-53-36/37
AU6200000
|Warning|H361 (100%): Suspected of damaging fertility or the unborn child [Warning Reproductive toxicity]|P201, P202, P281, P308+P313, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Drug Information
Drugs that are chemically similar to naturally occurring metabolites, but differ enough to interfere with normal metabolic pathways. (From AMA Drug Evaluations Annual, 1994, p2033) (See all compounds classified as Antimetabolites.)|Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)
9 beta Arabinofuranosyladenine
Computed Properties
Molecular Weight:285.26
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:2
Exact Mass:285.10731860
Monoisotopic Mass:285.10731860
Topological Polar Surface Area:141
Heavy Atom Count:20
Complexity:335
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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