Filibuvir

Filibuvir

SCHEMBL1464441

CCc1cc(CC[C@]2(C3CCCC3)CC(O)=C(Cc3nc4nc(C)cc(C)n4n3)C(=O)O2)cc(CC)n1

nearest known ligand 0.39

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NS5b

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.38
RECQL P46063 1/20 0.35
PDE10A Q9Y233 9/20 0.35
ALDH1A1 P00352 1/20 0.34
HTT P42858 1/20 0.34
KDM4E B2RXH2 1/20 0.34
KMT2A Q03164 1/20 0.33
TP53 P04637 2/20 0.32
POLB P06746 2/20 0.32
RXFP1 Q9HBX9 1/20 0.32

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
Filibuvir SCHEMBL12748294 1.00 TSHR (0.38) TSHRRECQLPDE10AALDH1A1HTT
Filibuvir SCHEMBL1053035 1.00 TSHR (0.38) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL1581540 0.98 TSHR (0.37) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL12340576 0.94 PDE10A (0.34) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL1581724 0.93 TSHR (0.34) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL1581447 0.93 TSHR (0.41) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL1581419 0.92 TSHR (0.38) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL3988230 0.92 TSHR (0.38) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL3985567 0.91 TSHR (0.37) TSHRRECQLPDE10AALDH1A1HTT
SCHEMBL14032061 0.91 TSHR (0.35) TSHRRECQLPDE10AALDH1A1HTT

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

Claimed or disclosed in 377 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
EP-4566670-A2 MODULATORS OF PHARMACOKINETIC PROPERTIES OF THERAPEUTICS Gilead Sciences, Inc. (US) 2025-06-11 EP claimed
US-20250032621-A1 DRUG CONJUGATE, PHARMACEUTICAL COMPOSITION AND METHOD OF TREATING HEPATITIS SeeCure Taiwan Co., Ltd. (TW) 2025-01-30 US claimed
EP-4483906-A1 DRUG CONJUGATE, PHARMACEUTICAL COMPOSITION AND METHOD OF TREATING HEPATITIS SeeCure Taiwan Co., Ltd. (TW) 2025-01-01 EP claimed
EP-4403221-A2 MODULATORS OF PHARMACOKINETIC PROPERTIES OF THERAPEUTICS Gilead Sciences, Inc. (US) 2024-07-24 EP claimed
WO-2024017234-A1 SALT OF HCV INHIBITOR, CRYSTAL FORM OF SALT, PHARMACEUTICAL COMPOSITION OF SALT, AND USE OF SALT 广东东阳光药业股份有限公司 2024-01-25 WO claimed
CN-117417327-A Salt of HCV inhibitor, crystalline form of salt, pharmaceutical composition thereof and use thereof 广东东阳光药业股份有限公司 2024-01-19 CN claimed
US-20230372370-A1 USE OF CANNABINOIDS IN THE TREATMENT OF COVID-19 Orcosa Inc. (US) 2023-11-23 US claimed
US-11752166-B2 Combination therapy for treatment of HCV COCRYSTAL PHARMA, INC. (US) 2023-09-12 US claimed
EP-3790542-B1 COMBINATION THERAPY FOR TREATMENT OF HCV COCRYSTAL PHARMA INC (US) 2023-07-19 EP claimed
EP-4114384-A1 METHODS OF INHIBITING SARS-COV-2 REPLICATION AND TREATING CORONAVIRUS DISEASE 2019 Pfizer Inc. (US) 2023-01-11 EP claimed
EP-2680859-B1 COMPOSITIONS, METHODS OF TREATMENT AND DIAGNOSTICS FOR TREATMENT OF HEPATIC STEATOSIS ALONE OR IN COMBINATION WITH A HEPATITIS C VIRUS INFECTION SCHENTAG JEROME (US) 2022-04-27 EP claimed
US-20220099672-A1 Method for Treating and/or Preventing Bacteriophage Lysis During Fermentation LOCUS SOLUTIONS, LLC 2022-03-31 US claimed
EP-3963087-A1 IDENTIFICATION AND ANALYSIS OF MICROBIAL SAMPLES BY RAPID INCUBATION AND NUCLEIC ACID ENRICHMENT Illumina Inc (US) 2022-03-09 EP claimed
WO-2021176369-A1 METHODS OF INHIBITING SARS-COV-2 REPLICATION AND TREATING CORONAVIRUS DISEASE 2019 PFIZER INC. (US) 2021-09-10 WO claimed
EP-4747381-A1 COMPOSITIONS AND METHODS FOR INHIBITING EXPRESSION OF PD-L1 Shanghai Argo Biopharmaceutical Co., Ltd. (CN) 2026-05-27 EP disclosed
WO-2026101522-A1 2'-FLUORO-6'METHYLENE CARBOCYCLIC NUCLEOSIDES AND NUCLEOTIDES AND METHODS OF TREATING POXVIRUS INFECTIONS WITH SAME UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2026-05-15 WO disclosed
EP-1928878-A1 METHODS FOR THE PREPARATION OF HCV POLYMERASE INHIBITORS PFIZER INC. (US) 2008-06-11 EP disclosed
WO-2007023381-A1 METHODS FOR THE PREPARATION OF HCV POLYMERASE INHIBITORS PFIZER INC. (US) 2007-03-01 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11752166-B2 Combination therapy for treatment of HCV HAVCR2, EIF2AK2, SERPINB1 TSHR 3386/4885RECQL 1797/4885PDE10A 4099/4885
US-20250032621-A1 DRUG CONJUGATE, PHARMACEUTICAL COMPOSITION AND METHOD OF TREATING HEPATITIS XIAP, BIRC5, BIRC7 TSHR 3147/4885RECQL 2411/4885PDE10A 3884/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.