(2S)-cyclo-Pentyl2-((((2R,3R,4R,5R)-5-(4-Aminopyrrolo[1,2-f][1,2,4]triazin-7-yl)-5-cyano-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(phenoxy)phosphorylamino)-propanoate

ID: ALA3120787

PubChem CID: 58059533

Max Phase: Preclinical

Molecular Formula: C27H33N6O8P

Molecular Weight: 600.57

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  C[C@H](NP(=O)(OC[C@H]1O[C@@](C#N)(c2ccc3c(N)ncnn23)[C@](C)(O)[C@@H]1O)Oc1ccccc1)C(=O)OC1CCCC1

Standard InChI:  InChI=1S/C27H33N6O8P/c1-17(25(35)39-18-8-6-7-9-18)32-42(37,41-19-10-4-3-5-11-19)38-14-21-23(34)26(2,36)27(15-28,40-21)22-13-12-20-24(29)30-16-31-33(20)22/h3-5,10-13,16-18,21,23,34,36H,6-9,14H2,1-2H3,(H,32,37)(H2,29,30,31)/t17-,21+,23+,26+,27-,42?/m0/s1

Standard InChI Key:  AEVVVSRGWZCNOJ-YNVDLFDSSA-N

Molfile:  

     RDKit          2D

 42 46  0  0  0  0  0  0  0  0999 V2000
    4.9711  -24.4619    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    5.3796  -23.7542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5624  -23.7542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7632  -26.5431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6710  -27.3551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4203  -27.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9461  -26.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0193  -25.7619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3547  -25.2834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6959  -25.7655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9186  -25.5134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2435  -24.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4649  -27.2027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1941  -23.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7381  -24.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9800  -23.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0087  -24.6913    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.7287  -25.0728    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.4205  -24.6393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3877  -23.8201    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6673  -23.4423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6350  -22.6258    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.6905  -26.2232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3615  -26.6895    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7484  -24.7141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3640  -25.0090    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5867  -24.7568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9797  -25.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4165  -23.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2024  -25.0517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1499  -26.1032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9710  -23.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3840  -22.3402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9760  -21.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1579  -21.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7496  -22.3453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1599  -23.0496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5953  -25.5988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7935  -25.4307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3852  -26.1386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9323  -26.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6786  -26.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  1  3  2  0
  5  4  1  0
  4  6  1  1
  7  4  1  0
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10  7  1  0
 10 11  1  1
  8 12  1  1
  7 13  1  6
 12 17  1  0
 16 14  2  0
 14 15  1  0
 15 12  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 16  1  0
 21 22  1  0
 23 24  3  0
  8 23  1  0
 11 25  1  0
 25  1  1  0
  1 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  6
 28 30  1  0
 28 31  2  0
  2 32  1  0
 32 33  2  0
 33 34  1  0
 34 35  2  0
 35 36  1  0
 36 37  2  0
 37 32  1  0
 30 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 38  1  0
M  END

Associated Targets(Human)

Hepatocyte (2737 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver (3974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Caco-2 (12174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Huh-7 (12904 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Syrian golden hamster (1610 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis C virus (23859 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

Calculated Properties

Molecular Weight: 600.57Molecular Weight (Monoisotopic): 600.2097AlogP: 2.21#Rotatable Bonds: 10
Polar Surface Area: 203.55Molecular Species: NEUTRALHBA: 13HBD: 4
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.23CX Basic pKa: 0.65CX LogP: 1.51CX LogD: 1.51
Aromatic Rings: 3Heavy Atoms: 42QED Weighted: 0.19Np Likeness Score: 0.14

References

1. Cho A, Zhang L, Xu J, Lee R, Butler T, Metobo S, Aktoudianakis V, Lew W, Ye H, Clarke M, Doerffler E, Byun D, Wang T, Babusis D, Carey AC, German P, Sauer D, Zhong W, Rossi S, Fenaux M, McHutchison JG, Perry J, Feng J, Ray AS, Kim CU..  (2014)  Discovery of the first C-nucleoside HCV polymerase inhibitor (GS-6620) with demonstrated antiviral response in HCV infected patients.,  57  (5): [PMID:23547794] [10.1021/jm400201a]

Source