SCHEMBL862934

SCHEMBL862934

CC(=O)N[C@@H]1C[C@H]1c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 1.00
NPSR1 Q6W5P4 1/20 1.00
MTNR1A P48039 1/20 0.58
MTNR1B P49286 1/20 0.58
KDM1A O60341 10/20 0.55
CNR1 P21554 1/20 0.55
HRH3 Q9Y5N1 1/20 0.55
EPHX2 P34913 4/20 0.54
MAOB P27338 2/20 0.53
TLR2 O60603 1/20 0.52
TLR1 Q15399 1/20 0.52
NPC1 O15118 1/20 0.52
RAB9A P51151 1/20 0.52
MAOA P21397 1/20 0.51

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
SCHEMBL25021708 1.00 SMN1; SMN2 (1.00) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL1600902 1.00 SMN1; SMN2 (1.00) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL1197466 1.00 SMN1; SMN2 (1.00) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL13794162 1.00 SMN1; SMN2 (1.00) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL14544486 1.00 SMN1; SMN2 (1.00) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
Hydrochloric Acid SCHEMBL28254537 0.98 SMN1; SMN2 (0.96) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL12539724 0.86 SMN1; SMN2 (0.76) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL12539722 0.86 SMN1; SMN2 (0.76) SMN1; SMN2NPSR1MTNR1AMTNR1BKDM1A
SCHEMBL6154005 0.85 SMN1; SMN2 (0.73) SMN1; SMN2NPSR1KDM1ACNR1HRH3
SCHEMBL7980208 0.85 SMN1; SMN2 (0.73) SMN1; SMN2NPSR1KDM1ACNR1HRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3262036-B1 THERAPEUTIC PYRIDAZINE COMPOUNDS AND USES THEREOF GENENTECH INC (US) 2023-09-13 EP disclosed
US-20180086720-A1 THERAPEUTIC COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2018-03-29 US disclosed
US-9856254-B2 Alkoxy substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY (US) 2018-01-02 US disclosed
CN-106488915-A Cyclopropylamine as LSD1 inhibitor 因赛特公司 2017-03-08 CN disclosed
CN-106164066-A Cyclopropylamines as lsd1 inhibitors 因赛特公司 2016-11-23 CN disclosed
US-20160280707-A1 ALKOXY SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES CO (US) 2016-09-29 US disclosed
US-20160280707-A1 ALKOXY SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES CO (US) 2016-09-29 US disclosed
WO-2016138114-A1 THERAPEUTIC PYRIDAZINE COMPOUNDS AND USES THEREOF GENENTECH, INC. (US) 2016-09-01 WO disclosed
CN-103857393-B Cyclopropylamine is as LSD1 inhibitor 葛兰素史密斯克莱知识产权(第2 号)有限公司 2016-08-17 CN disclosed
US-9365567-B2 Alkoxy substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY (US) 2016-06-14 US disclosed
US-20090029988-A1 Hydroxyalkyl Substituted Imidazoquinolines COLEY PHARMACEUTICAL GROP, INC. (US) 2009-01-29 US disclosed
US-20090023720-A1 2-Amino 1H-Imidazo Ring Systems and Methods 3M INNOVATIVE PROPERTIES COMPANY 2009-01-22 US disclosed
US-20090023720-A1 2-Amino 1H-Imidazo Ring Systems and Methods 3M INNOVATIVE PROPERTIES COMPANY 2009-01-22 US disclosed
US-20080015184-A1 Urea Substituted Imidazopyridines, Imidazoquinolines, and Imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY (US) 2008-01-17 US disclosed
US-20080015184-A1 Urea Substituted Imidazopyridines, Imidazoquinolines, and Imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY (US) 2008-01-17 US disclosed
US-20070259881-A1 Substituted Imidazo Ring Systems and Methods COLEY PHARMACEUTICAL GROUP, INC. 2007-11-08 US disclosed
US-20070167476-A1 Piperazine, [1,4]Diazepane, [1,4]Diazocane, and [1,5]Diazocane fused imidazo ring compounds 3M INNOVATIVE PROPERTIES COMPANY 2007-07-19 US disclosed
US-20070167476-A1 Piperazine, [1,4]Diazepane, [1,4]Diazocane, and [1,5]Diazocane fused imidazo ring compounds 3M INNOVATIVE PROPERTIES COMPANY 2007-07-19 US disclosed
US-20070060754-A1 Alkoxy substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2007-03-15 US disclosed
US-20070060754-A1 Alkoxy substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2007-03-15 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 (8 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-20070060754-A1 Alkoxy substituted imidazoquinolines IL2, IFNG, IRF3 SMN1; SMN2 3463/4885NPSR1 4039/4885MTNR1A 1410/4885
US-20070259881-A1 Substituted Imidazo Ring Systems and Methods IL2, IL4, IRF3 SMN1; SMN2 3807/4885NPSR1 3420/4885MTNR1A 776/4885
US-20070167476-A1 Piperazine, [1,4]Diazepane, [1,4]Diazocane, and [1,5]Diazocane fused imidazo ring compounds IL4, IL2, IL5 SMN1; SMN2 3137/4885NPSR1 1508/4885MTNR1A 760/4885
US-20160280707-A1 ALKOXY SUBSTITUTED IMIDAZOQUINOLINES IL2, IFNG, IRF3 SMN1; SMN2 3463/4885NPSR1 4039/4885MTNR1A 1410/4885
US-20080015184-A1 Urea Substituted Imidazopyridines, Imidazoquinolines, and Imidazonaphthyridines IL2, EIF2AK2, IL4 SMN1; SMN2 3238/4885NPSR1 4479/4885MTNR1A 2910/4885
US-20180086720-A1 THERAPEUTIC COMPOUNDS AND USES THEREOF SMARCC1, SMARCC2, SMARCA4 SMN1; SMN2 176/4885NPSR1 3059/4885MTNR1A 1615/4885
US-20090023720-A1 2-Amino 1H-Imidazo Ring Systems and Methods IL2, IL2RA, IL4I1 SMN1; SMN2 2883/4885NPSR1 3338/4885MTNR1A 390/4885
US-20090029988-A1 Hydroxyalkyl Substituted Imidazoquinolines IFNG, IRF3, IFNAR1 SMN1; SMN2 4162/4885NPSR1 4627/4885MTNR1A 2545/4885

“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.