SCHEMBL344947

SCHEMBL344947

CC(C)(C)OC(=O)N1CCCC[C@H]1CN

nearest known ligand 0.50

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
PDE8B O95263 1/20 0.49
KDM1A O60341 1/20 0.44
ATM Q13315 2/20 0.44
HSD17B10 Q99714 1/20 0.44
HPGD P15428 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.41
EPHX1 P07099 1/20 0.41
ALDH1A1 P00352 1/20 0.41
CHEK2 O96017 1/20 0.41
PREP P48147 1/20 0.40
OPRD1 P41143 1/20 0.39

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
SCHEMBL80021 1.00 PDE8B (0.49) PDE8BKDM1AATMHSD17B10HPGD
SCHEMBL283705 1.00 PDE8B (0.49) PDE8BKDM1AATMHSD17B10HPGD
SCHEMBL20214777 0.98 PDE8B (0.48) PDE8BKDM1AATMHSD17B10HPGD
Hydrochloric Acid SCHEMBL3564519 0.98 PDE8B (0.48) PDE8BKDM1AATMHSD17B10HPGD
SCHEMBL20186804 0.98 PDE8B (0.48) PDE8BKDM1AATMHSD17B10HPGD
SCHEMBL337349 0.95 HSD17B10 (0.48) PDE8BATMHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL337037 0.95 HSD17B10 (0.48) PDE8BATMHSD17B10SMN1; SMN2ALDH1A1
SCHEMBL205359 0.95 HSD17B10 (0.48) PDE8BATMHSD17B10SMN1; SMN2ALDH1A1
Hydrochloric Acid SCHEMBL1027414 0.94 HSD17B10 (0.47) PDE8BATMHSD17B10SMN1; SMN2ALDH1A1
Hydrochloric Acid SCHEMBL1026857 0.94 HSD17B10 (0.47) PDE8BATMHSD17B10SMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12617779-B2 Self degradation-type CDK9 inhibitor prodrug and liposome encapsulating same Sumitomo Pharma Co., Ltd. (JP) 2026-05-05 US disclosed
EP-3710458-B1 IMMUNOPROTEASOME INHIBITORS PRINCIPIA BIOPHARMA INC (US) 2026-03-25 EP disclosed
EP-4580620-A2 PYRAZOLE AND IMIDAZOLE DERIVATIVES AS DUAL OREXIN AND KAPPA-OPIOID RECEPTORS MODULATORS, COMPOSITION, METHODS FOR TREATING NEUROLOGICAL AND PSYCHIATRIC DISORDERS Hager Biosciences, LLC (US) 2025-07-09 EP disclosed
US-12312370-B2 Immunoproteasome inhibitors PRINCIPIA BIOPHARMA INC. (US) 2025-05-27 US disclosed
US-20250034200-A1 Prodrugs of Neurosteroid Analogs and Uses Thereof UNIV EMORY (US) 2025-01-30 US disclosed
US-20240368138-A1 SELF DEGRADATION-TYPE CDK9 INHIBITOR PRODRUG AND LIPOSOME ENCAPSULATING SAME Sumitomo Pharma Co., Ltd. (JP) 2024-11-07 US disclosed
CN-115894447-B METTL3 inhibitors and uses thereof 成都先导药物开发股份有限公司 2024-10-01 CN disclosed
US-20240262830-A1 IRE1A MODULATORS AND USES THEREOF NIMBUS IASO, INC. 2024-08-08 US disclosed
EP-4393918-A1 SELF DEGRADATION-TYPE CDK9 INHIBITOR PRODRUG AND LIPOSOME ENCAPSULATING SAME Sumitomo Pharma Co., Ltd. (JP) 2024-07-03 EP disclosed
WO-2024138157-A1 NOVEL IMIDAZOQUINOLINES WITH IMMUNOSTIMULATORY EFFECTS SYNOVO GMBH (DE) 2024-06-27 WO disclosed
US-20060183745-A1 Vanilloid receptor ligands and their use in treatments AMGEN INC. 2006-08-17 US disclosed
WO-2006028904-A1 QUINAZOLINES USEFUL AS MODULATORS OF ION CHANNELS VERTEX PHARMACEUTICALS INCORPORATED (US) 2006-03-16 WO disclosed
EP-1289955-B1 PIPERIDINES FOR USE AS OREXIN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 2005-04-13 EP disclosed
US-20040143115-A1 N-aroyl cyclic amines SMITHKLINE BEECHAM LIMITED (GB) 2004-07-22 US disclosed
EP-1385845-A1 N-AROYL CYCLIC AMINES SMITHKLINE BEECHAM PLC (GB) 2004-02-04 EP disclosed
US-6677354-B2 TREATING SLEEP, BRAIN, SEXUAL, CARDIOVASCULAR, NERVOUS SYSTEM, PSYCHOLOGICAL, GLANDULAR, AND GASTROINTESTINAL DISORDERS SMITHKLINE BEECHAM P.L.C. (GB) 2004-01-13 US disclosed
US-20030186964-A1 Piperdines for use as orexin receptor antagonists SMITHKLINE BEECHAM P.L.C. (GB) 2003-10-02 US disclosed
EP-1289955-A1 PIPERIDINES FOR USE AS OREXIN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 2003-03-12 EP disclosed
WO-2002090355-A1 N-AROYL CYCLIC AMINES SMITHKLINE BEECHAM P.L.C. (GB) 2002-11-14 WO disclosed
WO-2001096302-A1 PIPERIDINES FOR USE AS OREXIN RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM P.L.C. (GB) 2001-12-20 WO 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-12617779-B2 Self degradation-type CDK9 inhibitor prodrug and liposome encapsulating same CDK9, CDK6, CDK19 PDE8B 1651/4885KDM1A 36/4885ATM 1753/4885
US-12312370-B2 Immunoproteasome inhibitors PSMC2, PSMB7, PSMB2 PDE8B 3177/4885KDM1A 410/4885ATM 3544/4885
US-20240262830-A1 IRE1A MODULATORS AND USES THEREOF XBP1, HSPA5, ERN2 PDE8B 2008/4885KDM1A 3551/4885ATM 3391/4885
US-20060183745-A1 Vanilloid receptor ligands and their use in treatments TRPV1, TRPV2, TRPV3 PDE8B 2614/4885KDM1A 3574/4885ATM 2722/4885
US-20250034200-A1 Prodrugs of Neurosteroid Analogs and Uses Thereof CYP11B2, CYP11B1, CYP21A2 PDE8B 1258/4885KDM1A 3301/4885ATM 2713/4885
US-20040143115-A1 N-aroyl cyclic amines HCRTR1, HCRTR2, CNR1 PDE8B 3137/4885KDM1A 522/4885ATM 4061/4885
US-20240368138-A1 SELF DEGRADATION-TYPE CDK9 INHIBITOR PRODRUG AND LIPOSOME ENCAPSULATING SAME CDK9, CDK19, CDK6 PDE8B 1686/4885KDM1A 40/4885ATM 1500/4885
US-20030186964-A1 Piperdines for use as orexin receptor antagonists HCRTR2, HCRTR1, NPSR1 PDE8B 4562/4885KDM1A 1254/4885ATM 4837/4885

“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.