SCHEMBL741631

SCHEMBL741631

CN1CCc2ncsc2C1

nearest known ligand 0.54

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 9/20 0.54
DRD3 P35462 9/20 0.54
MAPK1 P28482 1/20 0.50
GRM5 P41594 2/20 0.41
CYP2C19 P33261 2/20 0.40
FGFR1 P11362 1/20 0.39
FGFR2 P21802 1/20 0.39
HRH3 Q9Y5N1 2/20 0.35
MAOA P21397 3/20 0.35
MAOB P27338 3/20 0.35
DRD1 P21728 1/20 0.35
DRD4 P21917 1/20 0.35
DRD5 P21918 1/20 0.35
SLC6A4 P31645 1/20 0.34

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
SCHEMBL12363792 0.86 DRD2 (0.66) DRD2DRD3MAPK1GRM5CYP2C19
Propionic Acid SCHEMBL29011051 0.86 MAPK1 (0.50) DRD2DRD3MAPK1GRM5CYP2C19
SCHEMBL740117 0.85 DRD2 (0.54) DRD2DRD3MAPK1GRM5CYP2C19
SCHEMBL742988 0.84
SCHEMBL1252787 0.81 MAPK1 (0.42) DRD2DRD3MAPK1GRM5
SCHEMBL27289803 0.78 DRD2 (0.59) DRD2DRD3MAPK1GRM5DRD4
SCHEMBL22736597 0.77 DRD2 (0.50) DRD2DRD3MAPK1GRM5FGFR1
SCHEMBL17613234 0.77 DRD2 (0.50) DRD2DRD3MAPK1GRM5FGFR1
SCHEMBL13937962 0.77 MAPK1 (0.47) DRD2DRD3MAPK1GRM5FGFR1
SCHEMBL13940002 0.77 DRD2 (0.58) DRD2DRD3MAPK1GRM5CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119552172-A Edison (R) sarban Synthesis method of intermediate 浙江美诺华药物化学有限公司 2025-03-04 CN claimed
CN-117384186-A Synthesis method of intermediate for preparing edoxaban 沧州那瑞化学科技有限公司 2024-01-12 CN claimed
US-7880005-B2 reacting 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine with an alkali metal nitrite in the presence of a reducing agent in an aqueous solution of an acidic compound; hydrolysis; industrial scale DAIICHI SANKYO COMPANY, LIMITED (JP) 2011-02-01 US claimed
US-20100076192-A1 PROCESS FOR PRODUCING 5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-c]PYRIDINE-2-CARBOXYLIC ACID DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2010-03-25 US claimed
US-12534474-B2 Dihydrofuropyridine derivatives as rho-kinase inhibitors CHIESI FARMACEUTICI S.P.A. (IT) 2026-01-27 US disclosed
CN-119751479-A Edison (R) sarban Synthesis method of intermediate 沧州那瑞化学科技有限公司 2025-04-04 CN disclosed
CN-119552172-A Edison (R) sarban Synthesis method of intermediate 浙江美诺华药物化学有限公司 2025-03-04 CN disclosed
CN-119552172-A Edison (R) sarban Synthesis method of intermediate 浙江美诺华药物化学有限公司 2025-03-04 CN disclosed
EP-4400497-A1 3CLPRO PROTEASE INHIBITOR Shanghai Qilu Pharmaceutical Research and Development Centre Ltd. (CN) 2024-07-17 EP disclosed
US-20240092792-A1 DIHYDROFUROPYRIDINE DERIVATIVES AS RHO- KINASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-03-21 US disclosed
US-20240082223-A1 DIHYDROFUROPYRIDINE DERIVATIVES AS RHO- KINASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-03-14 US disclosed
CN-117384186-A Synthesis method of intermediate for preparing edoxaban 沧州那瑞化学科技有限公司 2024-01-12 CN disclosed
US-20060004009-A1 Ethylenediamine derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2006-01-05 US disclosed
US-20050245565-A1 Diamine derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2005-11-03 US disclosed
EP-1577302-A1 NOVEL ETHYLENEDIAMINE DERIVATIVES DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2005-09-21 EP disclosed
US-20050119486-A1 Diamine derivatives DAIICHI SANKYO COMPANY, LIMITED (JP) 2005-06-02 US disclosed
US-20050020645-A1 Diamine derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2005-01-27 US disclosed
US-20040122063-A1 Ethylenediamine derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2004-06-24 US disclosed
EP-1405852-A1 DIAMINE DERIVATIVES DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2004-04-07 EP disclosed
EP-1270557-A1 ETHYLENEDIAMINE DERIVATIVES DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2003-01-02 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 (9 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-20100076192-A1 PROCESS FOR PRODUCING 5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-c]PYRIDINE-2-CARBOXYLIC ACID NOX4, NOX5, NOS2 DRD2 3556/4885DRD3 4485/4885MAPK1 719/4885
US-20060004009-A1 Ethylenediamine derivatives F2, ECE1, MLLT1 DRD2 702/4885DRD3 713/4885MAPK1 1349/4885
US-20050020645-A1 Diamine derivatives C9, C1S, C1R DRD2 351/4885DRD3 353/4885MAPK1 1864/4885
US-20240092792-A1 DIHYDROFUROPYRIDINE DERIVATIVES AS RHO- KINASE INHIBITORS ROCK1, ROCK2, RHOA DRD2 3255/4885DRD3 3530/4885MAPK1 263/4885
US-20050245565-A1 Diamine derivatives C9, C1S, C1R DRD2 351/4885DRD3 353/4885MAPK1 1864/4885
US-12534474-B2 Dihydrofuropyridine derivatives as rho-kinase inhibitors ROCK1, RHOC, ROCK2 DRD2 2801/4885DRD3 2229/4885MAPK1 119/4885
US-20050119486-A1 Diamine derivatives C9, C1S, C1R DRD2 351/4885DRD3 353/4885MAPK1 1864/4885
US-20240082223-A1 DIHYDROFUROPYRIDINE DERIVATIVES AS RHO- KINASE INHIBITORS ROCK1, ROCK2, RHOA DRD2 3255/4885DRD3 3530/4885MAPK1 263/4885
US-20040122063-A1 Ethylenediamine derivatives ECE1, F2, ECE2 DRD2 294/4885DRD3 283/4885MAPK1 987/4885

“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.