SCHEMBL6360274

SCHEMBL6360274

CCCNC(=O)c1cccc(Cl)c1

nearest known ligand 0.70

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.69
SMN1; SMN2 Q16637 2/20 0.63
POLB P06746 2/20 0.61
ALDH1A1 P00352 2/20 0.61
THRB P10828 1/20 0.58
RECQL P46063 1/20 0.58
TDP1 Q9NUW8 1/20 0.58
MEN1 O00255 2/20 0.57
KMT2A Q03164 2/20 0.57
TP53 P04637 1/20 0.57
TMEM97 Q5BJF2 1/20 0.56
SIGMAR1 Q99720 1/20 0.56
IDO1 P14902 1/20 0.56
KCNH2 Q12809 1/20 0.56
MAPT P10636 2/20 0.56
P2RX7 Q99572 1/20 0.56
NAMPT P43490 1/20 0.56

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
SCHEMBL6358483 0.90 SMN1; SMN2 (0.79) L3MBTL1SMN1; SMN2MEN1KMT2ATMEM97
SCHEMBL6543983 0.89 SMN1; SMN2 (0.71) L3MBTL1SMN1; SMN2MEN1KMT2ATMEM97
SCHEMBL13763531 0.88 L3MBTL1 (0.80) L3MBTL1SMN1; SMN2POLBALDH1A1MEN1
SCHEMBL9489991 0.86 NAMPT (0.70) SMN1; SMN2MEN1KMT2ATMEM97SIGMAR1
SCHEMBL4154673 0.86 ALDH1A1 (0.56) SMN1; SMN2POLBALDH1A1MEN1KMT2A
SCHEMBL9491028 0.86 NAMPT (0.70) SMN1; SMN2MEN1KMT2ATMEM97SIGMAR1
SCHEMBL1928910 0.83 ERN1 (0.63) L3MBTL1SMN1; SMN2POLBALDH1A1THRB
SCHEMBL12443610 0.83 SMN1; SMN2 (0.62) SMN1; SMN2MEN1KMT2ATMEM97SIGMAR1
SCHEMBL5020958 0.82 FABP4 (0.62) L3MBTL1SMN1; SMN2POLBALDH1A1THRB
Hydrochloric Acid SCHEMBL9584249 0.82 MEN1 (0.66) SMN1; SMN2POLBMEN1KMT2ATMEM97

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118771989-A Method for catalyzing hydrosilation reduction of amide into amine by using tridentate nitrogen ligand manganese complex 浙江工业大学 2024-10-15 CN disclosed
US-8168654-B2 Quinuclidine derivatives binding to mucarinic M3 receptors NOVARTIS AG (CH) 2012-05-01 US disclosed
US-8168654-B2 Quinuclidine derivatives binding to mucarinic M3 receptors NOVARTIS AG (CH) 2012-05-01 US disclosed
US-20100041887-A1 QUINUCLIDINE DERIVATIVES BINDING TO MUCARINIC M3 RECEPTORS COLLINGWOOD STEPHEN PAUL 2010-02-18 US disclosed
US-20100041887-A1 QUINUCLIDINE DERIVATIVES BINDING TO MUCARINIC M3 RECEPTORS COLLINGWOOD STEPHEN PAUL 2010-02-18 US disclosed
US-7576117-B1 Cyclic amine CCR3 antagonist TEIJIN LIMITED (JP) 2009-08-18 US disclosed
US-20070060563-A1 Quinuclidine derivatives binding to mucarinic m3 receptors NOVARTIS AG (CH) 2007-03-15 US disclosed
US-20070060563-A1 Quinuclidine derivatives binding to mucarinic m3 receptors NOVARTIS AG (CH) 2007-03-15 US disclosed
CN-1067215-C Composition of mouse expelling agent containing amide SHENYANG CHEMICAL INST MINISTR (CN) 2001-06-20 CN disclosed
US-4683330-A ANTICOAGULANTS, ANTIULCER AGENTS THE UPJOHN COMPANY (US) 1987-07-28 US disclosed
US-4160095-A PROSTAGLANDINS; ANTIINFLAMMATORY AGENTS THE UPJOHN COMPANY (US) 1979-07-03 US disclosed
US-4157441-A PROSTAGLANDINS, ANTIINFLAMMATORY AGENTS THE UPJOHN COMPANY (US) 1979-06-05 US disclosed
US-4151351-A PROSTAGLANDINS, ANTIINFLAMMATORY THE UPJOHN COMPANY (US) 1979-04-24 US disclosed
US-4131738-A 6-Hydroxy-PGE1 compounds THE UPJOHN COMPANY (US) 1978-12-26 US disclosed
US-4128713-A 6,7-Didehydro-PGI1 compounds THE UPJOHN COMPANY (US) 1978-12-05 US disclosed
US-4126744-A PROSTACYCLIN, MUSCLE STIMULANTS, PLATELET AGGREGATION INHIBITORS THE UPJOHN COMPANY (US) 1978-11-21 US disclosed
US-4112224-A PROSTAGLANDIN THE UPJOHN COMPANY (US) 1978-09-05 US disclosed
US-4109082-A PROSTACYCLIN ANALOGS; SMOOTH MUSCLE STIMULATORS THE UPJOHN COMPANY (US) 1978-08-22 US disclosed
US-4100192-A Inter-phenylene-PG amides THE UPJOHN COMPANY (US) 1978-07-11 US disclosed
US-4097489-A PROSTAGLANDINS THE UPJOHN COMPANY (US) 1978-06-27 US 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 (2 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-20070060563-A1 Quinuclidine derivatives binding to mucarinic m3 receptors CHRM3, CHRM2, CHRM1 L3MBTL1 3806/4885SMN1; SMN2 3865/4885POLB 4046/4885
US-20100041887-A1 QUINUCLIDINE DERIVATIVES BINDING TO MUCARINIC M3 RECEPTORS CHRM3, CHRM2, CHRM1 L3MBTL1 3806/4885SMN1; SMN2 3865/4885POLB 4046/4885

“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.