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9-beta-D-Arabinofuranosyladenine-5'-monophosphate Hydrate - 95%, high purity , CAS No.29984-33-6

COA

Grade & Purity:

≥95%

Cas Number: 29984-33-6
Molecular Weight: 347.22（Anhydrous）
PubChem CID: 34768
PubChem SID: 488183255

In stock

Item Number

D303366

Grouped product items
SKU	Size	Availability	Price
D303366-1g	1g	6	$20.90
D303366-5g	5g	4	$94.90
D303366-25g	25g	4	$425.90
D303366-100g	100g	2	$1,530.90

Adenosine analog antiviral agent

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Anti-infection (2803) Antibiotic (1629) HBV (114) Virus (1811)

Basic Description

Synonyms	9-beta-D-Arabinofuranosyladenine 5'-phosphate \| 9-(5-O-Phosphono-beta-D-arabinofuranosyl)adenine \| 9-(5-O-Phosphono-beta-D-arabinofuranosyl)-9H-purin-6-amine \| AS-70487 \| araAMP \| Ara-AMP \| 106XV160TZ \| 9-(.beta.-D-Arabinofuranosyl)adenine-5'-phosphate \|
Specifications & Purity	≥95%
Biochemical and Physiological Mechanisms	Adenosine analog antiviral agent. Highly soluble Vidarabine derivative. Disrupts viral DNA synthesis. Competitive viral DNA polymerase inhibitor. Active against herpes simplex and varicella zoster viruses in vivo .
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Purine nucleotides
    - Subclass Purine ribonucleotides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Purine nucleotides
Subclass	Purine ribonucleotides
Intermediate Tree Nodes	Not available
Direct Parent	Purine ribonucleoside monophosphates
Alternative Parents	Pentose phosphates Glycosylamines 6-aminopurines Monosaccharide phosphates Monoalkyl phosphates Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Heteroaromatic compounds Tetrahydrofurans 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Primary amines
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Alkyl phosphate - Monosaccharide - Pyrimidine - Imidolactam - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Tetrahydrofuran - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Organonitrogen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

Homo sapiens (32628 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Human alphaherpesvirus 2 (4932 Activities)

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Oryctolagus cuniculus (11301 Activities)

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FM3A (1296 Activities)

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L1210 (27553 Activities)

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Vero (26788 Activities)

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Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488183255
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488183255
IUPAC Name	[(2R,3S,4S,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
INCHI	InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6-,7+,10-/m1/s1
InChIKey	UDMBCSSLTHHNCD-UHTZMRCNSA-N
Smiles	C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O)N
Isomeric SMILES	C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
Molecular Weight	347.22（Anhydrous）
Reaxy-Rn	1229792
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1229792&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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8 results found

Lot Number	Certificate Type	Date	Item
D2303848	Certificate of Analysis	Feb 26, 2022	D303366
D2303865	Certificate of Analysis	Feb 26, 2022	D303366
D2303873	Certificate of Analysis	Feb 26, 2022	D303366
D2303849	Certificate of Analysis	Feb 26, 2022	D303366
D2303855	Certificate of Analysis	Feb 26, 2022	D303366
D2303861	Certificate of Analysis	Feb 26, 2022	D303366
D2303809	Certificate of Analysis	Feb 26, 2022	D303366
D2303864	Certificate of Analysis	Feb 26, 2022	D303366

Chemical and Physical Properties

Solubility	Soluble in water at 4mg/ml
Boil Point(°C)	798.5ºC
Melt Point(°C)	213ºC
Molecular Weight	347.220 g/mol
XLogP3	-3.500
Hydrogen Bond Donor Count	5
Hydrogen Bond Acceptor Count	11
Rotatable Bond Count	4
Exact Mass	347.063 Da
Monoisotopic Mass	347.063 Da
Topological Polar Surface Area	186.000 Å²
Heavy Atom Count	23
Formal Charge	0
Complexity	481.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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9-beta-D-Arabinofuranosyladenine-5'-monophosphate Hydrate - 95%, high purity , CAS No.29984-33-6

Basic Description

Taxonomic Classification

Associated Targets(Human)

Associated Targets(non-human)

Mechanisms of Action

Names and Identifiers

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

Chemical and Physical Properties

Solution Calculators

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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