(2S)-isopropyl 2-((((2S,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-fluoro-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphorylamino)propanoate

ID: ALA4476347

PubChem CID: 90248056

Max Phase: Preclinical

Molecular Formula: C26H31FN3O10P

Molecular Weight: 595.52

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CC(C)OC(=O)[C@H](C)NP(=O)(OC[C@@]1(F)O[C@@H](n2ccc(=O)[nH]c2=O)[C@](C)(O)[C@@H]1O)Oc1cccc2ccccc12

Standard InChI:  InChI=1S/C26H31FN3O10P/c1-15(2)38-21(32)16(3)29-41(36,40-19-11-7-9-17-8-5-6-10-18(17)19)37-14-26(27)22(33)25(4,35)23(39-26)30-13-12-20(31)28-24(30)34/h5-13,15-16,22-23,33,35H,14H2,1-4H3,(H,29,36)(H,28,31,34)/t16-,22-,23+,25+,26+,41?/m0/s1

Standard InChI Key:  AKVMLEWVOPUUDO-VNZXBQGSSA-N

Molfile:  

 
     RDKit          2D

 41 44  0  0  0  0  0  0  0  0999 V2000
   15.3904  -25.3701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8032  -26.0800    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   16.2116  -25.3676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.2105  -27.7226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5053  -27.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0926  -28.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2754  -28.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4623  -28.5027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5338  -27.7260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8709  -27.2438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2466  -27.3246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   19.9461  -27.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6561  -27.3438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6693  -26.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9663  -26.1078    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   19.2501  -26.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5465  -26.0912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3830  -26.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.0455  -29.2084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5100  -26.4929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0933  -26.4844    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.5732  -25.3725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9419  -25.3775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3570  -26.0863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1721  -26.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0886  -27.3016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3786  -27.7062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7940  -27.7142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6732  -27.2935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3739  -28.5233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6639  -28.9279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6592  -29.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9585  -28.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6798  -29.2084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5007  -28.1271    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
   13.3492  -24.6680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1622  -24.6694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5681  -23.9671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1621  -23.2629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3460  -23.2655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9437  -23.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  2  2  0
  8  7  1  0
  7  9  1  0
  9 10  1  0
 10  4  1  0
  4  8  1  0
  9 11  1  1
 11 12  1  0
 11 16  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 14 18  2  0
  7  6  1  1
  8 19  1  6
  4  5  1  1
  5 20  1  0
 20  2  1  0
  2 21  1  0
  1 22  1  0
 22 37  2  0
 36 23  2  0
 23 24  1  0
 24 25  2  0
 25 22  1  0
 21 26  1  0
 26 27  1  0
 26 28  1  1
 27 29  2  0
 27 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
  7 34  1  0
  4 35  1  0
 36 37  1  0
 37 38  1  0
 38 39  2  0
 39 40  1  0
 40 41  2  0
 41 36  1  0
M  END

Associated Targets(Human)

Huh-7 (12904 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hepatitis C virus (23859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Calculated Properties

Molecular Weight: 595.52Molecular Weight (Monoisotopic): 595.1731AlogP: 2.13#Rotatable Bonds: 10
Polar Surface Area: 178.41Molecular Species: NEUTRALHBA: 11HBD: 4
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.70CX Basic pKa: CX LogP: 1.95CX LogD: 1.95
Aromatic Rings: 3Heavy Atoms: 41QED Weighted: 0.20Np Likeness Score: 0.20

References

1. Wang G, Dyatkina N, Prhavc M, Williams C, Serebryany V, Hu Y, Huang Y, Wan J, Wu X, Deval J, Fung A, Jin Z, Tan H, Shaw K, Kang H, Zhang Q, Tam Y, Stoycheva A, Jekle A, Smith DB, Beigelman L..  (2019)  Synthesis and Anti-HCV Activities of 4'-Fluoro-2'-Substituted Uridine Triphosphates and Nucleotide Prodrugs: Discovery of 4'-Fluoro-2'- C-methyluridine 5'-Phosphoramidate Prodrug (AL-335) for the Treatment of Hepatitis C Infection.,  62  (9): [PMID:30951311] [10.1021/acs.jmedchem.9b00143]

Source