Tenofovir Disoproxil

Tenofovir Disoproxil

SCHEMBL40021

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

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 0.59
CYP2D6 P10635 14/20 0.53
ABCB11 O95342 1/20 0.49
POLA1 P09884 1/20 0.49
POLG P54098 1/20 0.49
SLC22A6 Q4U2R8 1/20 0.49

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 SCHEMBL16237284 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL985120 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL343783 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL3234290 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL2670560 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL29356301 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL18190782 1.00 FAP (1.00) FAPCYP3A4CYP2D6ABCB11POLA1
Tenofovir Disoproxil SCHEMBL3113154 0.97 FAP (0.94) FAPCYP3A4CYP2D6
Tenofovir Disoproxil SCHEMBL1560984 0.97 FAP (0.94) FAPCYP3A4CYP2D6
Tenofovir Disoproxil SCHEMBL497677 0.95 FAP (1.00) 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 13777 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
WO-2026102058-A1 METHODS FOR TREATING CHRONIC HEPATITIS B INFECTION AND RELATED FORMULATIONS TUNE THERAPEUTICS, INC. (US) 2026-05-15 WO claimed
EP-4735033-A2 MRNA-ENCODED TAT WITH ATTENUATED CYTOTOXICITY FOR HIV AND SIV LATENCY REVERSAL The Trustees of the University of Pennsylvania (US) 2026-05-06 EP claimed
EP-4444311-B1 GINSENOSIDES FOR TREATMENT OF CHRONIC HEPATITIS B VIRUS INFECTIONS MENDEL UNIV IN BRNO (CZ) 2026-05-06 EP claimed
WO-2026085583-A1 MOLECULAR ASSAY FOR DETECTING HIV-1 DRUG-RESISTANT MUTATIONS ST VINCENT'S HOSPITAL SYDNEY LIMITED (AU) 2026-04-30 WO claimed
EP-4732002-A2 MOLECULAR SIGNATURES OF LONG-TERM HEPATOCELLULAR CARCINOMA RISK IN NON-ALCOHOLIC FATTY LIVER DISEASE THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2026-04-29 EP claimed
US-12611453-B2 Method of inducing an HIV-1-specific immune response using a chimpanzee adenovirus vector encoding an hivacat t-cell immunogen and TLR7 agonist GILEAD SCIENCES, INC. (US) 2026-04-28 US claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US claimed
EP-4727950-A1 HETEROCYCLIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF MYCOBACTERIAL INFECTIONS GlaxoSmithKline Intellectual Property Development Ltd (GB) 2026-04-22 EP claimed
WO-2005000405-A2 P38 KINASE INHIBITOR COMPOSITIONS AND METHODS OF USE THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2005-01-06 WO claimed
US-20040224917-A1 Administering combination of [2-(6-amino-purin-9-yl)-1-methyl-ethoxymethyl]-phosphonic acid diisopropoxycarbonyloxymethyl ester fumarate (tenofovir disoproxil fumarate) and (2R, 5S, cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one (emtricitabine) GILEAD SCIENCES, INC. 2004-11-11 US claimed
US-20040224916-A1 Administering combination comprising 9-[R-2-[[(S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine (GS-7340) or a physiologically functional derivative thereof, and (2R,5S,cis)-4-amino-5-fluoro-1-(2-hydroxymethyl-1,3-oxathiolan-5-yl)-(1H)-pyrimidin-2-one (emtricitabine) GILEAD SCIENCES, INC. 2004-11-11 US claimed
US-20040208921-A1 Lipid-drug formulations and methods for targeted delivery of lipid-drug complexes to lymphoid tissues NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2004-10-21 US claimed
WO-2004064731-A2 LIPID-DRUG FORMULATIONS AND METHODS FOR TARGETED DELIVERY OF LIPID-DRUG COMPLEXES TO LYMLPLHOID TISSUES UNIVERSITY OF WASHINGTON (US) 2004-08-05 WO claimed
WO-2004064846-A1 COMPOSITIONS AND METHODS FOR COMBINATION ANTIVIRAL THERAPY GILEAD SCIENCES, INC. (US) 2004-08-05 WO claimed
WO-2004064845-A1 COMPOSITIONS AND METHODS FOR COMBINATION ANTIVIRAL THERAPY GILEAD SCIENCES, INC. (US) 2004-08-05 WO claimed
CN-1503669-A Antiviral agents and methods of treating viral infections ά�¶�ҩƷ��˾ 2004-06-09 CN claimed
US-20020188011-A1 Antiviral agents and methods of treating viral infections NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2002-12-12 US claimed
WO-2002085358-A2 ANTIVIRAL AGENTS AND METHODS OF TREATING VIRAL INFECTIONS VION PHARMACEUTICALS, INC. (US) 2002-10-31 WO claimed