SCHEMBL622419

SCHEMBL622419

CC(C)(C)OC(=O)NC1CCC(CC(=O)O)CC1

nearest known ligand 0.51

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
BTK Q06187 1/20 0.51
DRD2 P14416 7/20 0.48
KDM1A O60341 1/20 0.48
MAOB P27338 1/20 0.48
EPHX1 P07099 1/20 0.46
CTSK P43235 3/20 0.44
DRD3 P35462 1/20 0.44
GAA P10253 1/20 0.43
KMT2A Q03164 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
KCNA3 P22001 1/20 0.42
CTSS P25774 1/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41

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
SCHEMBL697088 1.00 BTK (0.51) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL1543495 1.00 BTK (0.51) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL6643451 0.91 BTK (0.56) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL16856527 0.91 BTK (0.56) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL3900948 0.91 BTK (0.56) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL28480020 0.87 DRD2 (0.48) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL30942791 0.87 DRD2 (0.48) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL1067922 0.86 BTK (0.50) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL13202379 0.86 DRD2 (0.47) BTKDRD2KDM1AMAOBEPHX1
SCHEMBL946942 0.86 BTK (0.50) BTKDRD2KDM1AMAOBEPHX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113527227-B Preparation method of kalirazine 四川弘远药业有限公司 2024-06-21 CN claimed
CN-117800875-A Preparation method of trans- (N-Boc-4-aminocyclohexyl) acetic acid 泰州精英化成医药科技有限公司 2024-04-02 CN claimed
CN-114539184-A Preparation method of cariprazine intermediate 泰州精英化成医药科技有限公司 2022-05-27 CN claimed
CN-114213362-A Preparation method of cariprazine and intermediate compound 成都栩哲医药科技有限公司 2022-03-22 CN claimed
CN-113527227-A Preparation method of cariprazine 成都弘达药业有限公司 2021-10-22 CN claimed
CN-113493399-A Preparation method for converting configuration of key intermediate of cariprazine 北京万全德众医药生物技术有限公司 2021-10-12 CN claimed
US-12630512-B2 Agents for differentiating stem cells and treating cancer MINERVA BIOTECHNOLOGIES CORPORATION (US) 2026-05-19 US disclosed
US-12583839-B2 PD-L1 antagonist compound ADLAI NORTYE BIOPHARMA CO., LTD. (CN) 2026-03-24 US disclosed
EP-3600451-B1 AGENTS FOR DIFFERENTIATING STEM CELLS AND TREATING CANCER MINERVA BIOTECHNOLOGIES CORP (US) 2025-12-24 EP disclosed
WO-2025230799-A2 CYCLOALKYL- AND PIPERIDINYL-CONTAINING DIAMINOMETHYLENE PYRIMIDINE-2,4,6-TRIONE AGONISTS OF PARATHYROID HORMONE 1 AND INCRETIN RECEPTORS SEPTERNA, INC. (US) 2025-11-06 WO disclosed
EP-4608810-A1 COMPOUNDS, COMPOSITIONS AND METHODS OF USE TO TREAT HYPOPARATHYROIDISM AND OSTEOPOROSIS Septerna, Inc. (US) 2025-09-03 EP disclosed
US-20250236632-A1 BETA-LACTAMASE INHIBITORS VENATORX PHARMACEUTICALS INC (US) 2025-07-24 US disclosed
WO-2025151602-A1 HETEROARYL COMPOUNDS AS LIGAND DIRECTED DEGRADERS OF IRAK4 BRISTOL-MYERS SQUIBB COMPANY (US) 2025-07-17 WO disclosed
US-20030018059-A1 Serine protease inhibitors PROTHERICS MOLECULAR DESIGN LIMITED (GB) 2003-01-23 US disclosed
EP-1119562-A1 2,3-DIHYDRO-1H-ISOINDOLE DERIVATIVES USEFUL AS MODULATORS OF DOPAMINE D3 RECEPTORS (ANTIPSYCHOTIC AGENTS) SMITHKLINE BEECHAM PLC (GB) 2001-08-01 EP disclosed
EP-1086095-A1 TETRAHYDROISOQUINOLINE DERIVATIVES AS MODULATORS OF DOPAMINE D3 RECEPTORS SMITHKLINE BEECHAM PLC (GB) 2001-03-28 EP disclosed
WO-2000021950-A1 2,3-DIHYDRO-1H-ISOINDOLE DERIVATIVES USEFUL AS MODULATORS OF DOPAMINE D3 RECEPTORS (ANTIPSYCHOTIC AGENTS) SMITHKLINE BEECHAM P.L.C. (GB) 2000-04-20 WO disclosed
WO-1999064412-A1 TETRAHYDROISOQUINOLINE DERIVATIVES AS MODULATORS OF DOPAMINE D3 RECEPTORS SMITHKLINE BEECHAM P.L.C. (GB) 1999-12-16 WO disclosed
US-5977110-A Substituted cyclohexylamines as central nervous systems agents WARNER-LAMBERT COMPANY (US) 1999-11-02 US disclosed
WO-1997011070-A1 SUBSTITUTED CYCLOHEXYLAMINES AS CENTRAL NERVOUS SYSTEM AGENTS WARNER-LAMBERT COMPANY (US) 1997-03-27 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 (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-20250236632-A1 BETA-LACTAMASE INHIBITORS MGAM, GAA, LCT BTK 524/4885DRD2 3783/4885KDM1A 447/4885
US-20030018059-A1 Serine protease inhibitors TPSAB1, PRSS1, SERPINB1 BTK 2793/4885DRD2 3971/4885KDM1A 876/4885
US-12630512-B2 Agents for differentiating stem cells and treating cancer MCL1, POU2F1, NES BTK 4615/4885DRD2 1863/4885KDM1A 723/4885
US-12583839-B2 PD-L1 antagonist compound CD274, PDCD1LG2, PDCD1 BTK 2199/4885DRD2 201/4885KDM1A 921/4885

“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.