SCHEMBL102874

SCHEMBL102874

CN1CCC(O)(C[N+](=O)[O-])CC1

nearest known ligand 0.35

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.35
LMNA P02545 1/20 0.32
THRB P10828 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.30
ALDH1A1 P00352 1/20 0.30
HPGD P15428 1/20 0.30
SIRT6 Q8N6T7 1/20 0.30

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
SCHEMBL17714536 0.77 ALDH1A1 (0.31) SMN1; SMN2LMNAALDH1A1
SCHEMBL1140913 0.76 ALDH1A1 (0.31) ALDH1A1
SCHEMBL1140855 0.76
SCHEMBL13919892 0.76 SIRT6 (0.30) SIRT6
SCHEMBL506476 0.74 L3MBTL1 (0.47) SMN1; SMN2LMNAL3MBTL1ALDH1A1
SCHEMBL307525 0.74
SCHEMBL11651593 0.74 CYP2C19 (0.33)
SCHEMBL10521581 0.71 DRD2 (0.31)
SCHEMBL1140929 0.71
Methane SCHEMBL27480548 0.71 L3MBTL1 (0.32) L3MBTL1ALDH1A1HPGDSIRT6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114507184-B Synthesis method and application of 1-methyl hexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2024-02-13 CN claimed
CN-114507184-A Synthesis method and application of 1-methylhexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2022-05-17 CN claimed
US-20250320217-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINES AS PROTEIN KINASE INHIBITORS SUMITOMO PHARMA AMERICA INC (US) 2025-10-16 US disclosed
US-20250129085-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINES AS PROTEIN KINASE INHIBITORS SUMITOMO PHARMA AMERICA INC (US) 2025-04-24 US disclosed
CN-114507184-B Synthesis method and application of 1-methyl hexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2024-02-13 CN disclosed
CN-114507184-B Synthesis method and application of 1-methyl hexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2024-02-13 CN disclosed
CN-114507184-A Synthesis method and application of 1-methylhexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2022-05-17 CN disclosed
CN-114507184-A Synthesis method and application of 1-methylhexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2022-05-17 CN disclosed
US-20210238183-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINES AS PROTEIN KINASE INHIBITORS SUMITOMO PHARMA AMERICA, INC. 2021-08-05 US disclosed
EP-3812387-A1 HETEROCYCLIC PROTEIN KINASE INHIBITORS Sumitomo Dainippon Pharma Oncology, Inc. (US) 2021-04-28 EP disclosed
US-10875864-B2 Substituted imidazo[1,2-B]pyridazines as protein kinase inhibitors SUMITOMO DAINIPPON PHARMA ONCOLOGY, INC. (US) 2020-12-29 US disclosed
EP-0452101-B1 Spiro bridged and unbridged heterocyclic compounds ISRAEL INST BIOLOG RES (IL) 1999-07-07 EP disclosed
EP-0888356-A1 CONDENSED 2,3-BENZODIAZEPINE DERIVATIVES AND THEIR USE AS AMPA-RECEPTOR INHIBITORS SCHERING AKTIENGESELLSCHAFT (DE) 1999-01-07 EP disclosed
US-5852029-A Aza spiro compounds acting on the cholinergic system with muscarinic agonist activity ISRAEL INSTITUTE FOR BIOLOGICAL RESEARCH (IL) 1998-12-22 US disclosed
WO-1997028163-A1 CONDENSED 2,3-BENZODIAZEPINE DERIVATIVES AND THEIR USE AS AMPA-RECEPTOR INHIBITORS SCHERING AKTIENGESELLSCHAFT (DE) 1997-08-07 WO disclosed
US-5534520-A Spiro compounds containing five-membered rings ISRAEL INSTITUTE FOR BIOLOGICAL RESEARCH (IL) 1996-07-09 US disclosed
EP-0711292-A1 AZA SPIRO COMPOUNDS ACTING ON THE CHOLINERGIC SYSTEM WITH MUSCARINIC AGONIST ACTIVITY KOSMIN, Gerald, Emmanuel (GB) 1996-05-15 EP disclosed
US-5407938-A Treating central nervous system disorders; Alzheimer*s ISRAEL INSTITUTE FOR BIOLOGICAL RESEARCH (IL) 1995-04-18 US disclosed
WO-1995003303-A2 AZA SPIRO COMPOUNDS ACTING ON THE CHOLINERGIC SYSTEM WITH MUSCARINIC AGONIST ACTIVITY STATE OF ISRAEL, REPRESENTED BY THE PRIME MINISTER'S OFFICE, ISRAEL INSTITUTE FOR BIOLOGICAL RESEARCH (IL) 1995-02-02 WO disclosed
EP-0452101-A2 Spiro bridged and unbridged heterocyclic compounds ISRAEL INSTITUTE FOR BIOLOGICAL RESEARCH (IL) 1991-10-16 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 (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-10875864-B2 Substituted imidazo[1,2-B]pyridazines as protein kinase inhibitors PIM2, PIM1, PIM3 SMN1; SMN2 3207/4885LMNA 1927/4885THRB 2910/4885
US-20210238183-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINES AS PROTEIN KINASE INHIBITORS PIM1, PIM2, PIM3 SMN1; SMN2 3075/4885LMNA 2351/4885THRB 703/4885
US-20250129085-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINES AS PROTEIN KINASE INHIBITORS PIM1, PIM2, PIM3 SMN1; SMN2 3075/4885LMNA 2351/4885THRB 703/4885
US-20250320217-A1 SUBSTITUTED IMIDAZO[1,2-B]PYRIDAZINES AS PROTEIN KINASE INHIBITORS PIM1, PIM2, PIM3 SMN1; SMN2 3075/4885LMNA 2351/4885THRB 703/4885

“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.