SCHEMBL507149

SCHEMBL507149

NCc1ccc2ncccc2c1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.58
MAPT P10636 2/20 0.58
ATM Q13315 2/20 0.58
KDM4E B2RXH2 1/20 0.58
TP53 P04637 1/20 0.58
HSP90AA1 P07900 1/20 0.58
HSP90AB1 P08238 1/20 0.58
TSHR P16473 1/20 0.58
CASP1 P29466 1/20 0.58
HTT P42858 1/20 0.58
SMN1; SMN2 Q16637 1/20 0.58
HSD17B10 Q99714 1/20 0.58
NPC1 O15118 3/20 0.57
RAB9A P51151 2/20 0.57
POLB P06746 1/20 0.57
DYRK1A Q13627 1/20 0.50
HDAC3 O15379 2/20 0.49
MET P08581 4/20 0.49
DAO P14920 1/20 0.49
CHKA P35790 1/20 0.48

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
SCHEMBL30586439 1.00 ALDH1A1 (0.58) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL29673226 1.00 ALDH1A1 (0.58) ALDH1A1MAPTATMKDM4ETP53
Iodide SCHEMBL20524052 0.98 ALDH1A1 (0.56) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL2597877 0.85 ALDH1A1 (0.59) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL1495700 0.85 ALDH1A1 (0.53) ALDH1A1MAPTATMKDM4ETP53
Hydrochloric Acid SCHEMBL20562948 0.84 ALDH1A1 (0.58) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL19338490 0.81 NPC1 (0.57) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL21169605 0.81 NPC1 (0.57) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL2107923 0.81 NPC1 (0.57) ALDH1A1MAPTATMKDM4ETP53
SCHEMBL1721002 0.81 NPC1 (0.57) ALDH1A1MAPTATMKDM4ETP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116943730-B Method for preparing cyclic amine compound by catalyzing hydrogenation of pyridine and quinoline compound 浙江大学 2025-04-11 CN claimed
CN-116943730-A Method for preparing cyclic amine compound by catalyzing hydrogenation of pyridine and quinoline compound 浙江大学 2023-10-27 CN claimed
EP-0675111-A2 Process for the preparation of 6-hydroxymethyl-quinolines BASF AKTIENGESELLSCHAFT (DE) 1995-10-04 EP claimed
US-20250273719-A1 ION-EXCHANGE MEMBRANE, MEMBRANE ELECTRODE ASSEMBLY, CELL FOR REDOX FLOW BATTERY, AND REDOX FLOW BATTERY ASAHI KASEI KABUSHIKI KAISHA (JP) 2025-08-28 US disclosed
CN-116943730-B Method for preparing cyclic amine compound by catalyzing hydrogenation of pyridine and quinoline compound 浙江大学 2025-04-11 CN disclosed
US-20250099462-A1 Certain Triazolopyridines and Triazolopyrazines, Compositions Thereof and Methods of Use Therefor HUTCHISON MEDIPHARMA LTD (CN) 2025-03-27 US disclosed
EP-4516845-A1 ION EXCHANGE MEMBRANE, MEMBRANE ELECTRODE ASSEMBLY, CELL FOR REDOX FLOW BATTERIES, AND REDOX FLOW BATTERY Asahi Kasei Kabushiki Kaisha (JP) 2025-03-05 EP disclosed
WO-2024218632-A1 ERK PROTEIN KINASE INHIBITORS ARRAY BIOPHARMA INC. (US) 2024-10-24 WO disclosed
CN-115605477-B Pyrazolo [1,5-a ] pyridine derivative, preparation method, composition and application thereof 深圳众格生物科技有限公司 2024-07-05 CN disclosed
CN-118271197-A Cyclohexylamine derivative, and composition and application thereof 上海京新生物医药有限公司 2024-07-02 CN disclosed
CN-118271234-A Piperidine derivative, composition and application thereof 上海京新生物医药有限公司 2024-07-02 CN disclosed
CN-1237183-A 6-0-substituted ketolides with antibacterial activity ABBOTT CO (US) 1999-12-01 CN disclosed
EP-0929563-A1 6-O-SUBSTITUTED KETOLIDES HAVING ANTIBACTERIAL ACTIVITY Abbott Laboratories (US) 1999-07-21 EP disclosed
US-5866549-A MACROLIDE ANTIBIOTICS ABBOTT LABORATORIES (US) 1999-02-02 US disclosed
US-5807875-A OBESITY THERAPY DR. KARL THOMAE GMBH (DE) 1998-09-15 US disclosed
WO-1998009978-A1 6-O-SUBSTITUTED KETOLIDES HAVING ANTIBACTERIAL ACTIVITY ABBOTT LABORATORIES (US) 1998-03-12 WO disclosed
US-5616620-A HYPOTENSIVE AGENTS KARL THOMAE GMBH (DE) 1997-04-01 US disclosed
EP-0675111-A3 Process for the preparation of 6-hydroxymethyl-quinolines BASF AKTIENGESELLSCHAFT (DE) 1995-11-15 EP disclosed
EP-0675111-A2 Process for the preparation of 6-hydroxymethyl-quinolines BASF AKTIENGESELLSCHAFT (DE) 1995-10-04 EP disclosed
EP-0675111-A2 Process for the preparation of 6-hydroxymethyl-quinolines BASF AKTIENGESELLSCHAFT (DE) 1995-10-04 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-20250099462-A1 Certain Triazolopyridines and Triazolopyrazines, Compositions Thereof and Methods of Use Therefor KCNJ11, NISCH, CYP4Z1 ALDH1A1 337/4885MAPT 3267/4885ATM 4256/4885

“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.