SCHEMBL7096969

SCHEMBL7096969

NC(=O)Cc1c(-c2ccccc2)nc2ccccn12

nearest known ligand 0.66

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
NTRK1 P04629 1/20 0.56
CYP1A2 P05177 1/20 0.53
CYP2C9 P11712 1/20 0.53
CYP2C19 P33261 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
NPC1 O15118 1/20 0.53
RAB9A P51151 1/20 0.53
ALDH1A1 P00352 2/20 0.51
KDM4E B2RXH2 1/20 0.51
PKM P14618 1/20 0.51
HPGD P15428 1/20 0.51
HSD17B10 Q99714 1/20 0.51
GAA P10253 1/20 0.50
SLC2A1 P11166 1/20 0.50
PTGS1 P23219 1/20 0.50
PTGS2 P35354 1/20 0.50
STAT3 P40763 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
SCHEMBL6642308 0.89 KDM4E (0.47) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL6686729 0.88 NTRK1 (0.58) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL13341887 0.85 SMN1; SMN2 (0.56) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL13341895 0.85 NPC1 (0.56) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL22780401 0.83 NTRK1 (0.57) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL13341897 0.82 GABRB2 (0.62) CYP1A2CYP2C9CYP2C19SMN1; SMN2NPC1
SCHEMBL13341900 0.82 ALDH1A1 (0.61) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL3613601 0.80 SLC2A2 (0.69) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2
SCHEMBL8208 0.79 KDM4E (0.64) SMN1; SMN2NPC1RAB9AKDM4EGAA
SCHEMBL9242819 0.79 NPC1 (0.59) NTRK1CYP1A2CYP2C9CYP2C19SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1172364-B1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides DINAMITE DIPHARMA S P A IN ABB (IT) 2003-04-23 EP claimed
US-6384226-B2 REACTING 2-PHENYL-IMIDAZOLO(1,2-A)PYRIDINE WITH OXALIC ACID ESTER; REDUCTION; AMIDATION DINAMITE DIPHARMA S.P.A. (IT) 2002-05-07 US claimed
US-20020019528-A1 Process for the preparation of 2-phenyl-imidazo [1, 2-a] pyridine-3-acetamides DINAMITE DIPHARMA S.P.A. 2002-02-14 US claimed
EP-1172364-A1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides Dinamite Dipharma S.p.A. (in abbreviated form Dipharma S.p.A.) (IT) 2002-01-16 EP claimed
EP-1172364-B1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides DINAMITE DIPHARMA S P A IN ABB (IT) 2003-04-23 EP disclosed
EP-1172364-B1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides DINAMITE DIPHARMA S P A IN ABB (IT) 2003-04-23 EP disclosed
JP-2002167385-A MANUFACTURING METHOD OF 2-PHENYLIMIDAZO[1,2a]PYRIDINE-3- ACETAMIDES DINAMITE DIPHARMA SPA ABBREVIATED DIPHARMA SPA 2002-06-11 JP disclosed
US-6384226-B2 REACTING 2-PHENYL-IMIDAZOLO(1,2-A)PYRIDINE WITH OXALIC ACID ESTER; REDUCTION; AMIDATION DINAMITE DIPHARMA S.P.A. (IT) 2002-05-07 US disclosed
US-6384226-B2 REACTING 2-PHENYL-IMIDAZOLO(1,2-A)PYRIDINE WITH OXALIC ACID ESTER; REDUCTION; AMIDATION DINAMITE DIPHARMA S.P.A. (IT) 2002-05-07 US disclosed
US-20020019528-A1 Process for the preparation of 2-phenyl-imidazo [1, 2-a] pyridine-3-acetamides DINAMITE DIPHARMA S.P.A. 2002-02-14 US disclosed
US-20020019528-A1 Process for the preparation of 2-phenyl-imidazo [1, 2-a] pyridine-3-acetamides DINAMITE DIPHARMA S.P.A. 2002-02-14 US disclosed
EP-1172364-A1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides Dinamite Dipharma S.p.A. (in abbreviated form Dipharma S.p.A.) (IT) 2002-01-16 EP disclosed
EP-1172364-A1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides Dinamite Dipharma S.p.A. (in abbreviated form Dipharma S.p.A.) (IT) 2002-01-16 EP disclosed
EP-1172364-A1 A process for the preparation of 2-phenyl-imidazo[1,2-A]pyridine-3-acetamides Dinamite Dipharma S.p.A. (in abbreviated form Dipharma S.p.A.) (IT) 2002-01-16 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 (1 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-20020019528-A1 Process for the preparation of 2-phenyl-imidazo [1, 2-a] pyridine-3-acetamides OTC, ODC1, OXGR1 NTRK1 1921/4885CYP1A2 114/4885CYP2C9 300/4885

“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.