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AB144336

Psicofuranine, Adenosine analog

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MW 297.27 Da, Purity >98%. Adenosine analog. Antineoplastic and antibiotic agent. Blocks guanosine monophosphate synthesis. Inhibits xanthosine monophosphate. Reduces phosphate utilization in tumors. Shows antitumor effects and antibacterial activity in vivo. .
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Chemical Structure - Psicofuranine, Adenosine analog (AB144336)
  • Chemical Structure

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Chemical Structure - Psicofuranine, Adenosine analog (AB144336)

2D chemical structure image of ab144336, Psicofuranine, Adenosine analog

Key facts

CAS number

1874-54-0

Purity

>98%

Form

Solid

form

Source

Streptomyces sp.

Molecular weight

297.27 Da

Molecular formula

C<sub>1</sub><sub>1</sub>H<sub>1</sub><sub>5</sub>N<sub>5</sub>O<sub>5</sub>

PubChem

65086

Nature

Native

Solubility

Soluble in water to 100 mM

Soluble in DMSO

Biochemical name

Psicofuranine

Biological description

Adenosine analog. Antineoplastic and antibiotic agent. Blocks guanosine monophosphate synthesis. Inhibits xanthosine monophosphate. Reduces phosphate utilization in tumors. Shows antitumor effects and antibacterial activity in vivo.

Canonical smiles

C1=NC(=C2C(=N1)N(C=N2)C3(C(C(C(O3)CO)O)O)CO)N

Isomeric smiles

C1=NC(=C2C(=N1)N(C=N2)[C@]3([C@@H]([C@@H]([C@H](O3)CO)O)O)CO)N

InChi

InChI=1S/C11H15N5O5/c12-9-6-10(14-3-13-9)16(4-15-6)11(2-18)8(20)7(19)5(1-17)21-11/h3-5,7-8,17-20H,1-2H2,(H2,12,13,14)/t5-,7-,8-,11-/m1/s1

InChiKey

BNZYRKVSCLSXSJ-IOSLPCCCSA-N

IUPAC Name

(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-2,5-bis(hydroxymethyl)oxolane-3,4-diol

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Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months
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Product protocols

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Primary Antibodies

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Primary Antibodies

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Primary Antibodies

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