Lamivudine

Lamivudine

SCHEMBL465678

Nc1ccn(C2CSC(CO)O2)c(=O)n1

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 Lamivudine. 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
ALB P02768 3/20 1.00
LMNA P02545 3/20 1.00
PDE3A Q14432 3/20 1.00
CACNA1F O60840 2/20 1.00
MAPT P10636 2/20 1.00
CACNA1D Q01668 2/20 1.00
CACNA1S Q13698 2/20 1.00
CACNA1C Q13936 2/20 1.00
POLG P54098 3/20 0.62
THRB P10828 1/20 0.52
MTOR P42345 1/20 0.52
MDM2 Q00987 1/20 0.52
NCOA1 Q15788 1/20 0.52
NCOA3 Q9Y6Q9 1/20 0.52
PDE4D Q08499 1/20 0.49
SLC29A1 Q99808 1/20 0.49
POLB P06746 1/20 0.42
NT5E P21589 1/20 0.39
ADRB1 P08588 1/20 0.37
DNMT1 P26358 1/20 0.37

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
Lamivudine SCHEMBL3444480 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL109675 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL33979 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL12964486 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL2305925 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL2422788 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL2240686 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL12996723 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL2806818 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT
Lamivudine SCHEMBL13006083 1.00 ALB (1.00) ALBLMNAPDE3ACACNA1FMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6432966-B1 None US claimed
EP-2519243-B1 COMPOSITIONS AND METHODS FOR TREATING HEPATITIS B VIRUS INFECTION Zhou xiao-jian (US) 2015-04-22 EP claimed
US-20130324497-A1 COMPOSITIONS AND METHODS FOR TREATING HEPATITIS B VIRUS INFECTION Zhou xiao-jian (US) 2013-12-05 US claimed
EP-2358708-B1 OPTICAL RESOLUTION OF SUBSTITUTED 1.3-OXATHIOLANE NUCLEOSIDES HETERO RESEARCH FOUNDATION (IN) 2013-06-12 EP claimed
EP-1060182-B1 NOVEL PRODRUGS FOR PHOSPHORUS-CONTAINING COMPOUNDS METABASIS THERAPEUTICS INC (US) 2012-12-19 EP claimed
US-8158607-B2 Crystalline form of lamivudine LUPIN LIMITED (IN) 2012-04-17 US claimed
US-8080536-B2 Phosphorus-containing prodrugs METABASIS THERAPEUTICS, INC. (US) 2011-12-20 US claimed
US-20110245497-A1 OPTICAL RESOLUTION OF SUBSTITUTED 1, 3-OXATHIOLANE NUCLEOSIDES HETERO RESEARCH FOUNDATION (IN) 2011-10-06 US claimed
EP-2358708-A2 OPTICAL RESOLUTION OF SUBSTITUTED 1.3-OXATHIOLANE NUCLEOSIDES Hetero Research Foundation (IN) 2011-08-24 EP claimed
US-20110009356-A1 NOVEL PHOSPHORUS-CONTAINING PRODRUGS METABASIS THERAPEUTICS, INC. (US) 2011-01-13 US claimed
EP-0583274-A1 USE OF A 1,3-OXATHIOLAN DERIVATIVE FOR THE TREATMENT OF HEPATITIS B INFECTION THE WELLCOME FOUNDATION LIMITED (GB) 1994-02-23 EP claimed
WO-1994002154-A1 ANTIVIRAL COMBINATIONS GLAXO GROUP LIMITED (GB) 1994-02-03 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-0517145-A1 Crystalline oxathiolane derivatives GLAXO GROUP LIMITED (GB) 1992-12-09 EP claimed
WO-1992020344-A1 ANTIVIRAL COMBINATIONS CONTAINING NUCLEOSIDE ANALOGS GLAXO GROUP LIMITED (GB) 1992-11-26 WO claimed
EP-0513917-A1 Antiviral combinations containing nucleoside analogs GLAXO GROUP LIMITED (GB) 1992-11-19 EP claimed
WO-1992019246-A1 USE OF A 1,3-OXATHIOLAN DERIVATIVE FOR THE TREATMENT OF HEPATITIS B INFECTION THE WELLCOME FOUNDATION LIMITED OF UNICORN HOUSE (GB) 1992-11-12 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
EP-0494119-A1 Use of 1,3-oxathiolane nucleoside analogues in the treatment of hepatitis B BIOCHEM PHARMA INC. (CA) 1992-07-08 EP claimed
CN-1058214-A 1, 3-oxathiolane nucleoside analogues IAF BIOCHEM INT (CA) 1992-01-29 CN claimed

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

For each of this compound's patents that has machine-readable text (3 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-20130324497-A1 COMPOSITIONS AND METHODS FOR TREATING HEPATITIS B VIRUS INFECTION HAVCR2, APOBEC3B, SLC10A1 ALB 501/4885LMNA 1443/4885PDE3A 858/4885
US-20110009356-A1 NOVEL PHOSPHORUS-CONTAINING PRODRUGS PYGL, ALPI, SLC10A1 ALB 2647/4885LMNA 3305/4885PDE3A 446/4885
US-20110245497-A1 OPTICAL RESOLUTION OF SUBSTITUTED 1, 3-OXATHIOLANE NUCLEOSIDES NUDT1, PNP, TYMP ALB 1577/4885LMNA 2653/4885PDE3A 1808/4885

“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.