SCHEMBL4170737

SCHEMBL4170737

Cc1nc2c(N)cc(C(=O)OC(C)C)cn2c1C

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 3/20 0.39
CA1 P00915 3/20 0.39
CA2 P00918 3/20 0.39
CA7 P43166 3/20 0.39
CA9 Q16790 3/20 0.39
CA14 Q9ULX7 3/20 0.39
KMT2A Q03164 3/20 0.38
NPC1 O15118 2/20 0.38
RAB9A P51151 2/20 0.38
MEN1 O00255 2/20 0.38
ALDH1A1 P00352 6/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
CYP3A4 P08684 3/20 0.38
CYP2C9 P11712 3/20 0.38
CYP2D6 P10635 2/20 0.38
CYP1A2 P05177 1/20 0.38
CYP2C19 P33261 1/20 0.38
JMJD6 Q6NYC1 1/20 0.36
RECQL P46063 1/20 0.36
SRD5A1 P18405 1/20 0.35

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
SCHEMBL4165967 0.85 KDM4E (0.42) NPC1RAB9AALDH1A1L3MBTL1CYP3A4
Bromide SCHEMBL4880840 0.84 CYP3A4 (0.41) NPC1RAB9AALDH1A1L3MBTL1CYP3A4
SCHEMBL4169299 0.83 SMN1; SMN2 (0.44) CA12CA1CA2CA7CA9
SCHEMBL5254676 0.80 CYP3A4 (0.39) KMT2ANPC1RAB9AMEN1ALDH1A1
SCHEMBL4163641 0.80 CYP3A4 (0.49) KMT2ANPC1RAB9AALDH1A1CYP3A4
Bromide SCHEMBL7554050 0.79 CYP3A4 (0.48) KMT2ANPC1RAB9AALDH1A1CYP3A4
SCHEMBL4654873 0.77 ALDH1A1 (0.41) CA12CA1CA2CA7CA9
SCHEMBL6219463 0.75 CYP3A4 (0.47) NPC1RAB9ACYP3A4CYP2C9CYP2D6
SCHEMBL2368041 0.74 CYP3A4 (0.68) CYP3A4CYP2C9CYP2D6CYP1A2CYP2C19
SCHEMBL5261078 0.72 CYP3A4 (0.34) NPC1RAB9AALDH1A1CYP3A4CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060063797-A1 Process for preparing a substituted imidazopyridine compound ELMAN BJORN 2006-03-23 US claimed
EP-3481827-B1 IMIDAZO[1,2-A]PYRIDINE DERIVATIVES, METHODS FOR PREPARING THE SAME AND USE THEREOF JEIL PHARMACEUTICAL CO LTD (KR) 2021-11-03 EP disclosed
US-10696671-B2 Imidazo[1,2-A]pyridine derivatives, methods for preparing the same and use thereof JEIL PHARMACEUTICAL CO., LTD. (KR) 2020-06-30 US disclosed
US-20190152971-A1 Imidazo[1,2-A]Pyridine Derivatives, Methods for Preparing the Same and Use Thereof JEIL PHARMACEUTICAL CO., LTD. (KR) 2019-05-23 US disclosed
EP-3481827-A1 IMIDAZO[1,2-A]PYRIDINE DERIVATIVES, METHODS FOR PREPARING THE SAME AND USE THEREOF Jeil Pharmaceutical Co., Ltd. (KR) 2019-05-15 EP disclosed
WO-2018008929-A1 IMIDAZO[1,2-A]PYRIDINE DERIVATIVES, METHODS FOR PREPARING THE SAME AND USE THEREOF JEIL PHARMACEUTICAL CO.,LTD. (KR) 2018-01-11 WO disclosed
US-20090291977-A1 Chromane Derivatives Useful As Acid Pump Antagonists RAQUALIA PHARMA INC. (JP) 2009-11-26 US disclosed
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound ELMAN BJORN 2009-10-01 US disclosed
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound ELMAN BJORN 2009-10-01 US disclosed
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound ELMAN BJORN 2009-10-01 US disclosed
EP-1838309-B1 CHROMANE DERIVATIVES USEFUL AS ACID PUMP ANTAGONISTS PFIZER (US) 2008-08-20 EP disclosed
EP-1838309-A1 CHROMANE DERIVATIVES USEFUL AS ACID PUMP ANTAGONISTS Pfizer, Inc. (US) 2007-10-03 EP disclosed
WO-2006064339-A1 CHROMANE DERIVATIVES USEFUL AS ACID PUMP ANTAGONISTS PFIZER JAPAN INC. (JP) 2006-06-22 WO disclosed
US-20060063797-A1 Process for preparing a substituted imidazopyridine compound ELMAN BJORN 2006-03-23 US disclosed
US-6900324-B2 Process for preparing a substituted imidazopyridine compound ASTRAZENECA AB (SE) 2005-05-31 US disclosed
EP-1317455-B9 PROCESS FOR PREPARING A SUBSTITUTED IMIDAZOPYRIDINE COMPOUND ASTRAZENECA AB (SE) 2004-11-17 EP disclosed
EP-1317455-B1 PROCESS FOR PREPARING A SUBSTITUTED IMIDAZOPYRIDINE COMPOUND ASTRAZENECA AB (SE) 2004-08-04 EP disclosed
US-20040039013-A1 Process for preparing a substituted imidazopyridine compound ASTRAZENECA AB (SE) 2004-02-26 US disclosed
EP-1317455-A1 PROCESS FOR PREPARING A SUBSTITUTED IMIDAZOPYRIDINE COMPOUND AstraZeneca AB (SE) 2003-06-11 EP disclosed
WO-2002020523-A1 PROCESS FOR PREPARING A SUBSTITUTED IMIDAZOPYRIDINE COMPOUND ASTRAZENECA AB (SE) 2002-03-14 WO 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 (6 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-20060063797-A1 Process for preparing a substituted imidazopyridine compound NISCH, CYP1B1, CYP1A2 CA12 3749/4885CA1 4005/4885CA2 2860/4885
US-20090247755-A1 Process for Preparing a Substituted Imidazopyridine Compound NISCH, CYP1A2, CYP1B1 CA12 3638/4885CA1 4014/4885CA2 2746/4885
US-20040039013-A1 Process for preparing a substituted imidazopyridine compound CYP1B1, BRD1, SKP1 CA12 4143/4885CA1 3991/4885CA2 2791/4885
US-10696671-B2 Imidazo[1,2-A]pyridine derivatives, methods for preparing the same and use thereof HRH2, GIPR, HRH4 CA12 2800/4885CA1 958/4885CA2 732/4885
US-20090291977-A1 Chromane Derivatives Useful As Acid Pump Antagonists HRH2, HRH1, CHRND CA12 1259/4885CA1 1580/4885CA2 432/4885
US-20190152971-A1 Imidazo[1,2-A]Pyridine Derivatives, Methods for Preparing the Same and Use Thereof GIPR, PGC, VIP CA12 3460/4885CA1 1088/4885CA2 510/4885

“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.