Tenofovir Disoproxil

Tenofovir Disoproxil

SCHEMBL52793

CC(C)OC(=O)OCOP(=O)(CO[C@H](C)Cn1cnc2c(N)ncnc21)OCOC(=O)OC(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

Ppol

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

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
FAP Q12884 3/20 1.00
CYP3A4 P08684 14/20 0.66
CYP2D6 P10635 14/20 0.57
ABCB11 O95342 1/20 0.54
POLA1 P09884 1/20 0.54
POLG P54098 1/20 0.54
SLC22A6 Q4U2R8 1/20 0.54

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
Tenofovir Disoproxil SCHEMBL497677 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL18907027 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL29376425 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL19031793 0.99 FAP (0.98) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL15241296 0.98 FAP (0.96) FAPCYP3A4CYP2D6
Tenofovir Disoproxil SCHEMBL20421896 0.97 FAP (0.95) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL983652 0.97 FAP (0.95) FAPCYP3A4CYP2D6ABCB11POLA1
SCHEMBL16486193 0.96 FAP (0.93) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL22157305 0.96 FAP (0.93) FAPCYP3A4CYP2D6
SCHEMBL12317035 0.96 FAP (0.93) FAPCYP3A4CYP2D6ABCB11POLA1

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 9420 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026107341-A1 COMBINATION THERAPY FOR TREATING HEPATITIS B VIRUS (HBV) INFECTION Vir Biotechnology, Inc. (US) 2026-05-21 WO 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
EP-4094767-B1 NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO UNIV EMORY (US) 2026-05-20 EP claimed
CN-122070288-A Bridged tricyclic carbamoyl pyridone compounds and uses thereof 吉利德科学公司 2026-05-19 CN claimed
CN-122055369-A Bridged tricyclic carbamoyl pyridone compounds and uses thereof 吉利德科学公司 2026-05-15 CN claimed
CN-122055373-A Bridged tricyclic carbamoyl pyridone compounds and uses thereof 吉利德科学公司 2026-05-15 CN 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-4719608-A1 QUINAZOLINYL-INDAZOLE DERIVATIVES AS THERAPEUTIC COMPOUNDS FOR HIV GILEAD SCIENCES, INC. (US) 2026-04-08 EP claimed
EP-4720056-A1 SOLID FORMS OF COMPOUNDS USEFUL IN THE TREATMENT OF HIV GILEAD SCIENCES, INC. (US) 2026-04-08 EP claimed
EP-4719602-A1 ANTI-HIV COMPOUNDS GILEAD SCIENCES, INC. (US) 2026-04-08 EP claimed
EP-1357928-A2 A NOVEL PHARMACEUTICAL COMPOUND AND METHODS OF MAKING AND USING SAME New River Pharmaceuticals Inc. (US) 2003-11-05 EP claimed
CN-1446213-A Medicinal compositions containing propenone derivatives SHIONOGI & CO (JP) 2003-10-01 CN claimed
US-20030171406-A1 Medicinal compositions containing propenone derivatives SHIONOGI & CO., LTD (JP) 2003-09-11 US claimed
EP-1295879-A1 MEDICINAL COMPOSITIONS CONTAINING PROPENONE DERIVATIVES SHIONOGI & CO., LTD. (JP) 2003-03-26 EP claimed
WO-2003020200-A2 A NOVEL PHARMACEUTICAL COMPOUND AND METHODS OF MAKING AND USING SAME NEW RIVER PHARMACEUTICALS INC. (US) 2003-03-13 WO claimed
US-20020187957-A1 Time release reverse transcriptase inhibitors HALSTEAD BRUCE (US) 2002-12-12 US claimed
EP-0998480-B1 NUCLEOTIDE ANALOG COMPOSITION AND SYNTHESIS METHOD GILEAD SCIENCES INC (US) 2002-11-27 EP claimed
WO-2002070470-A2 BENZOPHENONES AS INHIBITORS OF REVERSE TRANSCRIPTASE SMITHKLINE BEECHAM CORPORATION (US) 2002-09-12 WO claimed
EP-0998480-A1 NUCLEOTIDE ANALOG COMPOSITION AND SYNTHESIS METHOD GILEAD SCIENCES, INC. (US) 2000-05-10 EP claimed
WO-1999005150-A1 NUCLEOTIDE ANALOG COMPOSITION AND SYNTHESIS METHOD GILEAD SCIENCES, INC. (US) 1999-02-04 WO claimed