Standard InChI: InChI=1S/C13H14N4O4/c1-2-13(11(20)10(19)8(5-18)21-13)9-4-3-7-12(14)15-6-16-17(7)9/h1,3-4,6,8,10-11,18-20H,5H2,(H2,14,15,16)/t8-,10-,11-,13+/m1/s1
Standard InChI Key: AOBXNRJISYWUOA-VUXODMRMSA-N
Associated Targets(Human)
HeLa 62764 Activities
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Huh-7 12904 Activities
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MRC5 9203 Activities
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HEp-2 3859 Activities
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MT4 17854 Activities
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Associated Targets(non-human)
Hepatitis C virus 23859 Activities
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Yellow fever virus 1530 Activities
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dengue virus type 2 2400 Activities
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West Nile virus 623 Activities
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Influenza A virus 11224 Activities
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Human respirovirus 3 1674 Activities
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SARS-CoV 424 Activities
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Coxsackievirus A21 10 Activities
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Vero 26788 Activities
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MDCK 10148 Activities
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Human orthopneumovirus 392 Activities
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Hepatitis C virus NS5B RNA-dependent RNA polymerase 3026 Activities
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Molecule Features
Natural Product: No
Oral: No
Chemical Probe: No
Parenteral: No
Molecule Type: Small molecule
Topical: No
First In Class: No
Black Box: No
Chirality: No
Availability: No
Prodrug: No
Drug Indications
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Properties
Molecular Weight: 290.28
Molecular Weight (Monoisotopic): 290.1015
AlogP: -1.75
#Rotatable Bonds: 2
Polar Surface Area: 126.13
Molecular Species: NEUTRAL
HBA: 8
HBD: 4
#RO5 Violations: 0
HBA (Lipinski): 8
HBD (Lipinski): 5
#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.36
CX Basic pKa: 0.61
CX LogP: -1.49
CX LogD: -1.49
Aromatic Rings: 2
Heavy Atoms: 21
QED Weighted: 0.48
Np Likeness Score: 0.39
References
1.Cho A, Saunders OL, Butler T, Zhang L, Xu J, Vela JE, Feng JY, Ray AS, Kim CU.. (2012) Synthesis and antiviral activity of a series of 1'-substituted 4-aza-7,9-dideazaadenosine C-nucleosides., 22 (8):[PMID:22446091][10.1016/j.bmcl.2012.02.105]
2.Siegel D, Hui HC, Doerffler E, Clarke MO, Chun K, Zhang L, Neville S, Carra E, Lew W, Ross B, Wang Q, Wolfe L, Jordan R, Soloveva V, Knox J, Perry J, Perron M, Stray KM, Barauskas O, Feng JY, Xu Y, Lee G, Rheingold AL, Ray AS, Bannister R, Strickley R, Swaminathan S, Lee WA, Bavari S, Cihlar T, Lo MK, Warren TK, Mackman RL.. (2017) Discovery and Synthesis of a Phosphoramidate Prodrug of a Pyrrolo[2,1-f][triazin-4-amino] Adenine C-Nucleoside (GS-5734) for the Treatment of Ebola and Emerging Viruses., 60 (5):[PMID:28124907][10.1021/acs.jmedchem.6b01594]
3.Mackman RL, Hui HC, Perron M, Murakami E, Palmiotti C, Lee G, Stray K, Zhang L, Goyal B, Chun K, Byun D, Siegel D, Simonovich S, Du Pont V, Pitts J, Babusis D, Vijjapurapu A, Lu X, Kim C, Zhao X, Chan J, Ma B, Lye D, Vandersteen A, Wortman S, Barrett KT, Toteva M, Jordan R, Subramanian R, Bilello JP, Cihlar T.. (2021) Prodrugs of a 1'-CN-4-Aza-7,9-dideazaadenosine C-Nucleoside Leading to the Discovery of Remdesivir (GS-5734) as a Potent Inhibitor of Respiratory Syncytial Virus with Efficacy in the African Green Monkey Model of RSV., 64 (8.0):[PMID:33835812][10.1021/acs.jmedchem.1c00071]