Emtricitabine, (+/-)-

Emtricitabine, (+/-)-

SCHEMBL122131

Nc1nc(=O)n(C2CSC(CO)O2)cc1F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

pol

The experimentally established mechanism targets of Emtricitabine, (+/-)-. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ALB P02768 3/20 1.00
POLG P54098 2/20 0.64
LMNA P02545 3/20 0.63
CACNA1F O60840 2/20 0.63
MAPT P10636 2/20 0.63
CACNA1D Q01668 2/20 0.63
CACNA1S Q13698 2/20 0.63
CACNA1C Q13936 2/20 0.63
PDE3A Q14432 2/20 0.63
DCK P27707 7/20 0.36
DNMT1 P26358 5/20 0.36
ADRB1 P08588 1/20 0.36
DNMT3B Q9UBC3 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33

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
Emtricitabine SCHEMBL267686 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL3230512 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL12202574 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL6903677 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL5427218 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL6362885 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL3722124 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL39708 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL22413085 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT
Emtricitabine SCHEMBL12662838 1.00 ALB (1.00) ALBPOLGLMNACACNA1FMAPT

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 4353 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260144879-A1 ANTI-VIRAL AND HEPATIC-TARGETED DRUGS AI-BIOPHARMA (FR) 2026-05-28 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
US-12576124-B2 Formulation of a conjugate of a tubulysin analog to a cell-binding molecule HANGZHOU DAC BIOTECH CO., LTD (CN) 2026-03-17 US claimed
EP-3212200-B2 USE OF AN INVERSE TRANSCRIPTASE INHIBITOR FOR THE TREATMENT AND PREVENTION OF DEGENERATIVE DISEASES CENTRE NAT RECH SCIENT (FR) 2025-12-24 EP claimed
US-20250339551-A1 AN ANTIBODY-DRUG CONJUGATE HAVING TWO OR MORE DIFFERENT FUNCTIONAL SMALL MOLECULES FOR ENHANCED TREATMENT OF REFRACTORY DISEASES HANGZHOU SEEHE BIOTECHNOLOGY CO., LTD (CN) 2025-11-06 US claimed
EP-4642492-A1 AN ANTIBODY-DRUG CONJUGATE HAVING TWO OR MORE FUNCTIONAL SMALL MOLECULE COMPOUNDS FOR ENHANCED TREATMENT OF REFRACTORY DISEASES Hangzhou Seehe Biotechnology Co., Ltd (CN) 2025-11-05 EP claimed
EP-4642484-A1 TARGETED TREATMENT OF PROSTATE CANCERS AND OTHER TUMORS BY AN ANTIBODY-DRUG CONJUGATE Hangzhou Seehe Biotechnology Co., Ltd (CN) 2025-11-05 EP claimed
US-20250283074-A1 CLUSTERIN OVEREXPRESSION IN ALZHEIMER’S DISEASE UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2025-09-11 US claimed
EP-4566670-A2 MODULATORS OF PHARMACOKINETIC PROPERTIES OF THERAPEUTICS Gilead Sciences, Inc. (US) 2025-06-11 EP claimed
CN-119838022-A Amatoxin conjugates containing branched linkers 杭州多禧生物科技有限公司 2025-04-18 CN claimed
WO-1995007086-A1 NUCLEOSIDES WITH ANTI-HEPATITIS B VIRUS ACTIVITY EMORY UNIVERSITY (US) 1995-03-16 WO claimed
WO-1994009793-A1 ENANTIOMERICALLY PURE β-D-DIOXOLANE NUCLEOSIDES WITH SELECTIVE ANTI-HEPATITIS B VIRUS ACTIVITY EMORY UNIVERSITY (US) 1994-05-11 WO claimed
EP-0575482-A1 ANTIVIRAL ACTIVITY AND RESOLUTION OF 2-HYDROXYMETHYL-5-(5-FLUOROCYTOSIN-1-YL)-1,3-OXATHIOLANE EMORY UNIVERSITY (US) 1993-12-29 EP claimed
EP-0574487-A1 USE OF 5-FLUORO-2'-DEOXY-3'-THIACYTIDINE FOR THE TREATMENT OF HEPATITIS B THE WELLCOME FOUNDATION LIMITED (GB) 1993-12-22 EP claimed
EP-0574457-A1 ANTIVIRAL NUCLEOSIDE COMBINATION THE WELLCOME FOUNDATION LIMITED (GB) 1993-12-22 EP claimed
US-5234913-A Synergistic mixture of 1-(2-(hydroxymethyl)-1,3-oxathiolan-5-yl)-5-fluorocystosine and zidovudine BURROUGHS WELLCOME CO. (US) 1993-08-10 US claimed
EP-0526253-A1 1,3-Oxathiolane nucleoside analogues BIOCHEM PHARMA INC. (CA) 1993-02-03 EP claimed
WO-1992015309-A1 ANTIVIRAL NUCLEOSIDE COMBINATION THE WELLCOME FOUNDATION LIMITED (GB) 1992-09-17 WO claimed
WO-1992015308-A1 USE OF 5-FLUORO-2'-DEOXY-3'-THIACYTIDINE FOR THE TREATMENT OF HEPATITIS B THE WELLCOME FOUNDATION LIMITED (GB) 1992-09-17 WO claimed
WO-1992014743-A2 ANTIVIRAL ACTIVITY AND RESOLUTION OF 2-HYDROXYMETHYL-5-(5-FLUOROCYTOSIN-1-YL)-1,3-OXATHIOLANE EMORY UNIVERSITY (US) 1992-09-03 WO claimed