SCHEMBL210949

SCHEMBL210949

Nc1c(Cl)nc2ccccc2c1N

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 8/20 0.64
ALDH1A1 P00352 4/20 0.64
HSD17B10 Q99714 4/20 0.64
KDM4E B2RXH2 4/20 0.64
GLA P06280 2/20 0.64
HPGD P15428 2/20 0.64
CASP1 P29466 2/20 0.64
CASP7 P55210 2/20 0.64
SMN1; SMN2 Q16637 2/20 0.64
TDP1 Q9NUW8 2/20 0.64
MAOA P21397 2/20 0.64
CHRM2 P08172 2/20 0.64
ADRA2A P08913 2/20 0.64
ADORA3 P0DMS8 2/20 0.64
CHRM1 P11229 2/20 0.64
SLC6A2 P23975 2/20 0.64
OPRM1 P35372 2/20 0.64
KCNH2 Q12809 2/20 0.64
NQO2 P16083 1/20 0.64
DRD1 P21728 1/20 0.64

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
SCHEMBL30583435 1.00 ACHE (0.64) ACHEALDH1A1HSD17B10KDM4EGLA
Hydrochloric Acid SCHEMBL843193 0.98 RAB9A (0.65) ACHEALDH1A1HSD17B10KDM4EGLA
SCHEMBL12874595 0.85 MAOA (0.61) ACHEALDH1A1HSD17B10KDM4EGLA
SCHEMBL15978466 0.82 ALDH1A1 (0.52) ACHEALDH1A1HSD17B10KDM4EGLA
Aminacrine SCHEMBL14999 0.79 HSD17B10 (1.00) ACHEALDH1A1HSD17B10KDM4EGLA
Aminacrine SCHEMBL29354393 0.79 HSD17B10 (1.00) ACHEALDH1A1HSD17B10KDM4EGLA
SCHEMBL16021109 0.77 KDM1A (0.47) ACHEALDH1A1HSD17B10KDM4EGLA
SCHEMBL4059507 0.77 HSD17B10 (0.52) ACHEALDH1A1HSD17B10KDM4EGLA
SCHEMBL29809559 0.77 HSD17B10 (0.70) ACHEALDH1A1HSD17B10KDM4EGLA
SCHEMBL841779 0.77 HSD17B10 (0.70) ACHEALDH1A1HSD17B10KDM4EGLA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4499641-A1 A3 ADENOSINE RECEPTOR POSITIVE ALLOSTERIC MODULATORS The United States of America, as represented by the Secretary, Department of Health and Human Services (US) 2025-02-05 EP disclosed
WO-2023192408-A1 A3 ADENOSINE RECEPTOR POSITIVE ALLOSTERIC MODULATORS THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2023-10-05 WO disclosed
WO-2023192408-A1 A3 ADENOSINE RECEPTOR POSITIVE ALLOSTERIC MODULATORS THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2023-10-05 WO disclosed
WO-2022161420-A1 CLASS OF HETEROAROMATIC COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF 上海翊石医药科技有限公司 2022-08-04 WO disclosed
EP-1948173-B1 HYDROXY AND ALKOXY SUBSTITUTED 1H-IMIDAZOQUINOLINES AND METHODS 3M INNOVATIVE PROPERTIES CO (US) 2013-07-17 EP disclosed
US-8377957-B2 Hydroxy and alkoxy substituted 1H-imidazoquinolines and methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2013-02-19 US disclosed
US-8143270-B2 2-amino 1H-in-imidazo ring systems and methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2012-03-27 US disclosed
US-20120071463-A1 HYDROXY AND ALKOXY SUBSTITUTED 1H-IMIDAZOQUINOLINES AND METHODS 3M INNOVATIVE PROPERTIES COMPANY 2012-03-22 US disclosed
US-8088790-B2 Hydroxy and alkoxy substituted 1H-imidazoquinolines and methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2012-01-03 US disclosed
US-7915281-B2 Isoxazole, dihydroisoxazole, and oxadiazole substituted imidazo ring compounds and method 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-03-29 US disclosed
EP-1339715-A2 HETEROCYCLIC ETHER SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2003-09-03 EP disclosed
US-20030139441-A1 Sulfonamido ether substituted imidazoquinolines UBS AG, STAMFORD BRANCH 2003-07-24 US disclosed
US-20030065005-A1 Heterocyclic ether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2003-04-03 US disclosed
US-20020193396-A1 Sulfonamido ether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2002-12-19 US disclosed
WO-2002046193-A2 HETEROCYCLIC ETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2002-06-13 WO disclosed
WO-2002046189-A2 ARYL ETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2002-06-13 WO disclosed
WO-2002046190-A2 SULFONAMIDO ETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2002-06-13 WO disclosed
US-5756747-A 1H-imidazo 4,5-c!quinolin-4-amines RIKER LABORATORIES, INC. (US) 1998-05-26 US disclosed
EP-0385630-B1 1H-imidazo(4,5-c)Quinolin-4-amines as antivirals RIKER LABORATORIES INC (US) 1996-11-27 EP disclosed
EP-0385630-A2 1H-imidazo(4,5-c)Quinolin-4-amines as antivirals RIKER LABORATORIES, INC. (US) 1990-09-05 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 (4 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-20030065005-A1 Heterocyclic ether substituted imidazoquinolines IFNG, IL2, IRF3 ACHE 4670/4885ALDH1A1 2486/4885HSD17B10 3488/4885
US-20030139441-A1 Sulfonamido ether substituted imidazoquinolines IFNG, IRF3, IL2 ACHE 4783/4885ALDH1A1 2448/4885HSD17B10 4364/4885
US-20120071463-A1 HYDROXY AND ALKOXY SUBSTITUTED 1H-IMIDAZOQUINOLINES AND METHODS IFNG, IL2, IRF3 ACHE 4256/4885ALDH1A1 517/4885HSD17B10 1013/4885
US-20020193396-A1 Sulfonamido ether substituted imidazoquinolines IFNG, IRF3, IL2 ACHE 4783/4885ALDH1A1 2448/4885HSD17B10 4364/4885

“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.