SCHEMBL1058152

SCHEMBL1058152

CCCCN(C=N)CCCC

nearest known ligand 0.33

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 3/20 0.33
TSHR P16473 2/20 0.33
LMNA P02545 1/20 0.33
CA12 O43570 3/20 0.32
CA1 P00915 3/20 0.32
CA9 Q16790 3/20 0.32
ALDH1A1 P00352 1/20 0.32
ALDH2 P05091 1/20 0.32
THRB P10828 1/20 0.32
MMP1 P03956 1/20 0.30
MMP2 P08253 1/20 0.30
MMP3 P08254 1/20 0.30
MMP8 P22894 1/20 0.30
CA2 P00918 1/20 0.30

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
SCHEMBL5419793 1.00 DNM1 (0.33) DNM1TSHRLMNACA12CA1
SCHEMBL7209887 0.82
SCHEMBL5412874 0.81
SCHEMBL5412878 0.81
SCHEMBL3952513 0.81 DNM1 (0.40) DNM1TSHRCA12CA1CA9
SCHEMBL5419798 0.77 DNM1 (0.33) DNM1TSHRLMNACA12CA1
SCHEMBL22472335 0.75 TSHR (0.38) DNM1TSHRLMNACA12CA1
SCHEMBL18165074 0.74
SCHEMBL182250 0.73 TSHR (0.35) DNM1TSHRLMNACA12CA1
SCHEMBL9485027 0.72 CA12 (0.34) DNM1TSHRLMNACA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1504014-B1 PROCESS FOR PREPARATION OF CYCLIC PRODRUGS OF PMEA AND PMPA METABASIS THERAPEUTICS INC (US) 2015-12-02 EP claimed
EP-2331558-A2 PROTECTED MONOMERS AND METHODS OF DEPROTECTION FOR RNA SYNTHESIS Agilent Technologies, Inc. (US) 2011-06-15 EP claimed
WO-2010034024-A2 PROTECTED MONOMERS AND METHODS OF DEPROTECTION FOR RNA SYNTHESIS AGILENT TECHNOLOGIES, INC. (US) 2010-03-25 WO claimed
US-20070203339-A1 Process for Preparation of Cyclic Prodrugs of PMEA and PMPA METABASIS THERAPEUTICS, INC. 2007-08-30 US claimed
US-7193081-B2 9-(2-(2,4-cis(S)-4-(3-chlorophenyl)-2-oxo-1,3,2-dioxaphosphor-inan-2 -yl)methoxyethyl)adenine by coupling the dichloridate of 9-(2-phosphonyl- methoxyethyl- or propyl)adenine (PMEA)(PMPA) with a 1-(chlorophenyl) propylene-1,3-diol METABASIS THERAPEUTICS, INC. (US) 2007-03-20 US claimed
EP-1504014-A4 PROCESS FOR PREPARATION OF CYCLIC PRODRUGS OF PMEA AND PMPA METABASIS THERAPEUTICS INC (US) 2006-06-07 EP claimed
EP-1504014-A2 PROCESS FOR PREPARATION OF CYCLIC PRODRUGS OF PMEA AND PMPA Metabasis Therapeutics, Inc. (US) 2005-02-09 EP claimed
US-20030225277-A1 Process for preparation of cyclic prodrugs of PMEA and PMPA METABASIS THERAPEUTICS, INC. 2003-12-04 US claimed
WO-2003095665-A2 PMEA AND PMPA CYCLIC PRODUCING SYNTHESIS METABASIS THERAPEUTICS, INC. (US) 2003-11-20 WO claimed
WO-1993025566-A1 DEUTERATED NUCLEOSIDES CHATTOPADHYAYA JYOTI (SE) 1993-12-23 WO claimed
EP-3818066-B1 DOUBLE COUPLING METHOD FOR OLIGONUCLEOTIDE SYNTHESIS AGILENT TECHNOLOGIES INC (US) 2022-06-15 EP disclosed
US-20210347645-A1 Macroporous Controlled Porosity Silica Gel Suitable For Oligonucleotide Synthesis CHEMGENES CORPORATION 2021-11-11 US disclosed
EP-3906997-A2 MACROPOROUS CONTROLLED POROSITY SILICA GEL SUITABLE FOR OLIGONUCLEOTIDE SYNTHESIS Chemgenes Corporation (US) 2021-11-10 EP disclosed
EP-3818066-A1 DOUBLE COUPLING METHOD FOR OLIGONUCLEOTIDE SYNTHESIS Agilent Technologies, Inc. (US) 2021-05-12 EP disclosed
US-10597421-B2 Protected monomer and method of final deprotection for RNA synthesis AGILENT TECHNOLOGIES, INC. (US) 2020-03-24 US disclosed
EP-1307469-A1 NUCLEIC ACID BINDING COMPOUNDS CONTAINING PYRAZOLO[3,4-D]PYRIMIDINE ANALOGUES OF PURIN-2,6-DIAMINE AND THEIR USES BOEHRINGER MANNHEIM GMBH (DE) 2003-05-07 EP disclosed
WO-2002012263-A1 NUCLEIC ACID BINDING COMPOUNDS CONTAINING PYRAZOLO[3,4-D]PYRIMIDINE ANALOGUES OF PURIN-2,6-DIAMINE AND THEIR USES ROCHE DIAGNOSTICS GMBH (DE) 2002-02-14 WO disclosed
US-6140496-A Precursors for deoxyribonucleotides containing non-standard nucleosides BENNER, STEVEN 2000-10-31 US disclosed
US-5264448-A Thioamides, oxazole ring, insecticides, miticides SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-11-23 US disclosed
EP-0394043-A1 An amide compound and its production and use SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1990-10-24 EP 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 (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-20030225277-A1 Process for preparation of cyclic prodrugs of PMEA and PMPA MPO, PNP, MAOA DNM1 2698/4885TSHR 3320/4885LMNA 883/4885
US-10597421-B2 Protected monomer and method of final deprotection for RNA synthesis NSUN2, RNGTT, RNMT DNM1 1470/4885TSHR 3650/4885LMNA 260/4885
US-20070203339-A1 Process for Preparation of Cyclic Prodrugs of PMEA and PMPA PNP, PHOSPHO1, MPO DNM1 2736/4885TSHR 3839/4885LMNA 913/4885

“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.