Favipiravir

Favipiravir

SCHEMBL587913

NC(=O)c1nc(F)cnc1O

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PAPB1PB2

The experimentally established mechanism targets of Favipiravir. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LCK P06239 1/20 0.34
KMT2A Q03164 2/20 0.32
MEN1 O00255 1/20 0.32
PDPK1 O15530 1/20 0.31
ADORA3 P0DMS8 1/20 0.31
TSHR P16473 1/20 0.31
MC4R P32245 1/20 0.31
ADRA1A P35348 1/20 0.31
MC3R P41968 1/20 0.31
IKBKB O14920 1/20 0.31
AURKA O14965 1/20 0.31
NNMT P40261 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
SIRT6 Q8N6T7 1/20 0.31
ADORA2A P29274 1/20 0.30
ADORA1 P30542 1/20 0.30
ALDH1A1 P00352 1/20 0.30
LMNA P02545 1/20 0.30
CLK1 P49759 1/20 0.30
DYRK1A Q13627 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Favipiravir SCHEMBL21085196 0.98 LCK (0.33) LCKKMT2AMEN1PDPK1ADORA3
Favipiravir SCHEMBL30725561 0.98 LCK (0.33) LCKKMT2AMEN1PDPK1ADORA3
Favipiravir SCHEMBL28964779 0.87 LMNA (0.32) LMNA
SCHEMBL5269681 0.84 PLAU (0.33) LCKKMT2APDPK1ADORA3TSHR
SCHEMBL31259490 0.84 PLAU (0.33) LCKKMT2APDPK1ADORA3TSHR
Favipiravir SCHEMBL28952948 0.82 PARP1 (0.38)
SCHEMBL28398570 0.82 KDM4E (0.37) KMT2AMEN1TSHRSMN1; SMN2ALDH1A1
SCHEMBL6376447 0.82 KMT2A (0.32) LCKKMT2AMEN1PDPK1ADORA3
SCHEMBL29733656 0.82 KMT2A (0.32) LCKKMT2AMEN1PDPK1ADORA3
SCHEMBL25028569 0.80

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 4545 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4228644-B1 N-[4-[1-(1,4-DIOXASPIRO[4.5]DEC-8-YL)-4-(8-OXA-3-AZABICYCLO[3.2.1]OCT-3-YL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-6-YL]PHENYL]-N'-METHYLUREA FOR USE IN THE TREATMENT OF COVID19 NANTCELL INC (US) 2026-05-27 EP claimed
US-20260139860-A1 PRODUCTS OF MANUFACTURE FOR THE TREATMENT, PREVENTION AND AMELIORATION OF MICROBIAL INFECTIONS CENTRE FOR DIGESTIVE DISEASES (AU) 2026-05-21 US claimed
US-20260139035-A1 HUMAN ANTIBODY AGAINST CORONAVIRUS VARIANTS OR ANTIGEN-BINDING FRAGMENT THEREOF NATIONAL UNIVERSITY CORPORATION KUMAMOTO UNIVERSITY (JP) 2026-05-21 US claimed
US-20260130921-A1 TREATMENT OF VIRAL INFECTIONS WITH COMBINATION OF PIKFYVE KINASE INHIBITORS AND TMPRSS-2 INHIBITORS AcuraStem Incorporated (US) 2026-05-14 US claimed
EP-4740962-A1 PHARMACEUTICAL COMPOSITION, FORMULATION CONTAINING PHARMACEUTICAL COMPOSITION, KIT CONTAINING PHARMACEUTICAL COMPOSITION, PREPARATION METHOD FOR PHARMACEUTICAL COMPOSITION, AND USE OF PHARMACEUTICAL COMPOSITION Shanghai WD Pharmaceutical Co., Ltd (CN) 2026-05-13 EP claimed
EP-4255391-B1 LUMINOL FOR USE IN THE TREATMENT OF SEQUELAE OF A SARS-COV-2 INFECTION METRIOPHARM AG (CH) 2026-05-06 EP claimed
EP-3790536-B1 NANOCONTAINERS FOR TRANSPORTING NONPOLAR, LIPOPHILIC SUBSTANCES SUCH AS ANTIBIOTICS KARLSRUHER INST TECHNOLOGIE (DE) 2026-04-22 EP claimed
US-12605378-B2 Small therapeutic molecules capable of inhibiting the catalytic activity of the main protease enzyme of SARS-CoV-2 ISTANBUL MEDIPOL UNIVERSITESI (TR) 2026-04-21 US claimed
US-20260102422-A1 4'-HALOGEN CONTAINING NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO UNIV EMORY (US) 2026-04-16 US claimed
EP-4725496-A2 N-[4-[1-(1,4-DIOXASPIRO[4.5]DEC-8-YL)-4-(8-OXA-3-AZABICYCLO[3.2.1]OCT-3-YL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-6-YL]PHENYL]-N'-METHYLUREA FOR USE IN THE TREATMENT OF COVID19 NantCell, Inc. (US) 2026-04-15 EP claimed
EP-2623498-A1 SODIUM SALT OF 6-FLUORO-3-HYDROXY-2-PYRAZINE CARBOXAMIDE Toyama Chemical Co., Ltd. (JP) 2013-08-07 EP claimed
CN-102775358-A Preparation method of 6-fluoro-3-hydroxy-2-pyrazinamide SHANDONG QIDU PHARMACEUTICAL 2012-11-14 CN claimed
CN-102655859-A Combination therapy treatment for viral infections GEMMUS PHARMA INC 2012-09-05 CN claimed
EP-2488168-A1 COMBINATION THERAPY TREATMENT FOR VIRAL INFECTIONS Gemmus Pharma Inc. (US) 2012-08-22 EP claimed
US-20120190637-A1 COMBINATION THERAPY TREATMENT FOR VIRAL INFECTIONS GEMMUS PHARMA, INC. (US) 2012-07-26 US claimed
CN-102603658-A Preparation method of 6-fluorine-3-hydroxyl-2-pyrazinamide SHANDONG QIDU PHARMACEUTICAL 2012-07-25 CN claimed
CN-102348458-A Tablet and granulated powder containing 6-fluoro-3-hydroxy-2-pyrazinecarboxamide TOYAMA CHEMICAL CO LTD 2012-02-08 CN claimed
EP-2407166-A1 TABLET AND GRANULATED POWDER CONTAINING 6-FLUORO-3-HYDROXY-2-PYRAZINECARBOXAMIDE Toyama Chemical Co., Ltd. (JP) 2012-01-18 EP claimed
US-20120010221-A1 TABLET AND GRANULATED POWDER CONTAINING 6-FLUORO-3-HYDROXY-2-PYRAZINECARBOXAMIDE TOYAMA CHEMICAL CO.,LTD. (JP) 2012-01-12 US claimed
WO-2011047048-A1 COMBINATION THERAPY TREATMENT FOR VIRAL INFECTIONS GEMMUS PHARMA, INC. (US) 2011-04-21 WO claimed