SCHEMBL4395941

SCHEMBL4395941

CCNC(=O)c1ccc(Cl)nc1

nearest known ligand 0.63

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.63
RAB9A P51151 4/20 0.60
SMN1; SMN2 Q16637 2/20 0.60
NPC1 O15118 2/20 0.60
KMT2A Q03164 5/20 0.57
MEN1 O00255 4/20 0.57
CACNA1B Q00975 1/20 0.57
APBA1 Q02410 1/20 0.57
ALDH1A1 P00352 1/20 0.57
LMNA P02545 1/20 0.57
MAPT P10636 2/20 0.56
PKM P14618 1/20 0.56
NAPRT Q6XQN6 1/20 0.55
POLB P06746 1/20 0.52
DGAT1 O75907 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
MDM4 O15151 1/20 0.50
TP53 P04637 1/20 0.50
MDM2 Q00987 1/20 0.50

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
Diethylamine SCHEMBL11263676 0.94 L3MBTL1 (0.57) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL3407381 0.87 RAB9A (0.65) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL9561524 0.84 ALDH1A1 (0.51) RAB9ASMN1; SMN2NPC1KMT2AMEN1
SCHEMBL25210162 0.84 L3MBTL1 (0.57) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL20460467 0.83 NPC1 (0.60) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL12456093 0.83 L3MBTL1 (0.63) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL17670950 0.82 L3MBTL1 (0.58) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL3409371 0.82 HPGD (0.59) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL3369793 0.82 L3MBTL1 (0.58) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A
SCHEMBL10645032 0.82 L3MBTL1 (0.58) L3MBTL1RAB9ASMN1; SMN2NPC1KMT2A

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230150972-A1 PYRIDINYL DERIVATIVES AS SODIUM CHANNEL ACTIVATORS XENON PHARMACEUTICALS INC. (CA) 2023-05-18 US disclosed
CN-107849053-B Spiro compounds 里科瑞尔姆IP控股有限责任公司 2020-10-30 CN disclosed
US-8492437-B2 4-substituted phenoxyphenylacetic acid derivatives ARRAY BIOPHARMA INC. (US) 2013-07-23 US disclosed
US-7943643-B2 Aryl substituted pyridines and the use thereof PURDUE PHARMA L.P. (US) 2011-05-17 US disclosed
US-7943643-B2 Aryl substituted pyridines and the use thereof PURDUE PHARMA L.P. (US) 2011-05-17 US disclosed
US-20100048626-A1 Aryl Substituted Pyridines and the Use Thereof PURDUE PHARMA L.P. 2010-02-25 US disclosed
US-20090306052-A1 INDENYL DERIVATIVES AND USE THEREOF FOR THE TREATMENT OF NEUROLOGICAL DISORDERS GLAXO GROUP LIMITED 2009-12-10 US disclosed
US-7579367-B2 Aryl substituted pyridines and the use thereof PURDUE PHARMA L.P. (US) 2009-08-25 US disclosed
US-20080194627-A9 Aryl substituted pyridines and the use thereof EURO-CELTIQUE S.A. (LU) 2008-08-14 US disclosed
CN-101115721-A Indenyl derivatives and their use in the treatment of neurological diseases GLAXO GROUP LTD (GB) 2008-01-30 CN disclosed
US-20070010554-A1 Aryl substituted pyridines and the use thereof EURO-CELTIQUE S.A. (LU) 2007-01-11 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 (5 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-20080194627-A9 Aryl substituted pyridines and the use thereof CACNA1S, CACNA1E, CACNA1C L3MBTL1 116/4885RAB9A 3343/4885SMN1; SMN2 7/4885
US-20100048626-A1 Aryl Substituted Pyridines and the Use Thereof CACNA1S, CACNA1E, CACNA1C L3MBTL1 129/4885RAB9A 3446/4885SMN1; SMN2 8/4885
US-20090306052-A1 INDENYL DERIVATIVES AND USE THEREOF FOR THE TREATMENT OF NEUROLOGICAL DISORDERS NLN, INMT, INA L3MBTL1 1592/4885RAB9A 1932/4885SMN1; SMN2 110/4885
US-20070010554-A1 Aryl substituted pyridines and the use thereof CACNA1S, CACNA1E, CACNA1C L3MBTL1 116/4885RAB9A 3343/4885SMN1; SMN2 7/4885
US-20230150972-A1 PYRIDINYL DERIVATIVES AS SODIUM CHANNEL ACTIVATORS SCN1B, SCN1A, SCN2B L3MBTL1 1776/4885RAB9A 628/4885SMN1; SMN2 564/4885

“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.