(2R)-methyl 2-((((2R,3S,4S,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(phenoxy)phosphorylamino)-3-methylbutanoate

ID: ALA475394

PubChem CID: 44572008

Max Phase: Preclinical

Molecular Formula: C22H29N6O8P

Molecular Weight: 536.48

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COC(=O)[C@H](NP(=O)(OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H](O)[C@@H]1O)Oc1ccccc1)C(C)C

Standard InChI:  InChI=1S/C22H29N6O8P/c1-12(2)15(22(31)33-3)27-37(32,36-13-7-5-4-6-8-13)34-9-14-17(29)18(30)21(35-14)28-11-26-16-19(23)24-10-25-20(16)28/h4-8,10-12,14-15,17-18,21,29-30H,9H2,1-3H3,(H,27,32)(H2,23,24,25)/t14-,15-,17-,18+,21-,37?/m1/s1

Standard InChI Key:  HPXBTPGTPDQDJY-ZEVZXRMJSA-N

Molfile:  

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M  END

Associated Targets(non-human)

Intestine (155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver (4264 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (10718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human alphaherpesvirus 1 (11089 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Biocomponents

Calculated Properties

Molecular Weight: 536.48Molecular Weight (Monoisotopic): 536.1784AlogP: 1.02#Rotatable Bonds: 10
Polar Surface Area: 193.17Molecular Species: NEUTRALHBA: 13HBD: 4
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.22CX Basic pKa: 4.92CX LogP: 0.55CX LogD: 0.55
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.21Np Likeness Score: 0.56

References

1. Shen W, Kim JS, Kish PE, Zhang J, Mitchell S, Gentry BG, Breitenbach JM, Drach JC, Hilfinger J..  (2009)  Design and synthesis of vidarabine prodrugs as antiviral agents.,  19  (3): [PMID:19097789] [10.1016/j.bmcl.2008.12.031]
2. Wang Z, Zang R, Niu Z, Wang W, Wang X, Tang Y..  (2021)  Synthesis and antiviral effect of phosphamide modified vidarabine for treating HSV 1 infections.,  52  [PMID:34624489] [10.1016/j.bmcl.2021.128405]

Source