SCHEMBL578028

SCHEMBL578028

CC(C)(C)OC(=O)N1CC=C(c2ccc(Br)cc2)CC1

nearest known ligand 0.60

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
NAMPT P43490 1/20 0.60
PDK4 Q16654 1/20 0.56
GRM1 Q13255 11/20 0.53
GRM5 P41594 11/20 0.53
CDK7 P50613 1/20 0.48
CDK13 Q14004 1/20 0.48
CDK12 Q9NYV4 1/20 0.48
HTR6 P50406 1/20 0.48
CYP11B2 P19099 1/20 0.47
TNK2 Q07912 1/20 0.46
JAK1 P23458 1/20 0.45
BTK Q06187 1/20 0.45

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
SCHEMBL8912847 0.89 NAMPT (0.63) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL904049 0.88 NAMPT (0.61) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL19459003 0.88 NAMPT (0.50) NAMPTPDK4GRM1GRM5HTR6
SCHEMBL1198658 0.87 NAMPT (0.53) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL30722230 0.87 NAMPT (0.53) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL18619842 0.86 NAMPT (0.60) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL18619845 0.86 NAMPT (0.60) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL29227506 0.86 NAMPT (0.60) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL2908091 0.86 NAMPT (0.60) NAMPTPDK4GRM1GRM5CDK7
SCHEMBL2594283 0.86 GRM1 (0.65) NAMPTPDK4GRM1GRM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260124309-A1 STAT6 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-05-07 US disclosed
EP-4713096-A1 CDK INHIBITOR COMPOUNDS Aleksia Therapeutics, Inc. (US) 2026-03-25 EP disclosed
US-12570650-B2 6-substituted pyridazine compounds as SMARCA2 and/or SMARCA4 degraders AURIGENE ONCOLOGY LIMITED (IN) 2026-03-10 US disclosed
US-12559492-B2 BRAF degraders C4 THERAPEUTICS, INC. (US) 2026-02-24 US disclosed
US-12479849-B2 EGFR inhibitors for the treatment of cancer HOFFMANN-LA ROCHE INC. (US) 2025-11-25 US disclosed
EP-4558495-A1 HETEROARYL COMPOUNDS AS LIGAND DIRECTED DEGRADERS OF IRAK4 Bristol-Myers Squibb Company (US) 2025-05-28 EP disclosed
WO-2025094065-A1 AMINO-SUBSTITUTED PYRIDAZINE COMPOUNDS AS SMARCA2 AND/OR SMARCA4 DEGRADERS AURIGENE ONCOLOGY LIMITED (IN) 2025-05-08 WO disclosed
US-20250145609-A1 3-SUBSTITUTED PYRIDAZINE COMPOUNDS AS SMARCA2 AND/OR SMARCA4 DEGRADERS AURIGENE ONCOLOGY LIMITED (IN) 2025-05-08 US disclosed
EP-4522617-A1 NEW INDAZOLE DERIVATIVES F. Hoffmann-La Roche AG (CH) 2025-03-19 EP disclosed
WO-2025049820-A1 STAT6 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. (US) 2025-03-06 WO disclosed
US-20070032469-A1 Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators ASTRAZENECA AB (SE) 2007-02-08 US disclosed
US-20070032469-A1 Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators ASTRAZENECA AB (SE) 2007-02-08 US disclosed
US-6774265-B2 SALT FORMATION REACTION OF PHOSPHINE AND SECONDARY PHOSPHINE IN ALCOHOLIC SOLVENT NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2004-08-10 US disclosed
US-20040138504-A1 BISPHOSPHONIUM SALT AND PROCESS FOR PRODUCING THE SAME NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2004-07-15 US disclosed
US-20040044008-A1 Use of therapeutic benzamide derivatives DAUGAN ALAIN CLAUDE-MARIE (FR) 2004-03-04 US disclosed
US-6552022-B1 Atherosclerosis in a mammal, pancreatitis, non-insulin dependent diabetes mellitus, coronary heart disease in a lowering serum lipid levels SMITHKLINE BEECHAM CORPORATION 2003-04-22 US disclosed
EP-1286670-A2 USE OF THERAPEUTIC BENZAMIDE DERIVATIVES GLAXO GROUP LIMITED (GB) 2003-03-05 EP disclosed
WO-2001097810-A2 USE OF THERAPEUTIC BENZAMIDE DERIVATIVES GLAXO GROUP LIMITED (GB) 2001-12-27 WO disclosed
EP-1135378-A1 BENZAMIDE DERIVATIVES AND THEIR USE AS APOB-100 SECRETION INHIBITORS GLAXO GROUP LIMITED (GB) 2001-09-26 EP disclosed
WO-2000032582-A1 BENZAMIDE DERIVATIVES AND THEIR USE AS APOB-100 SECRETION INHIBITORS GLAXO GROUP LIMITED (GB) 2000-06-08 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-20040138504-A1 BISPHOSPHONIUM SALT AND PROCESS FOR PRODUCING THE SAME PIP5K1B, PIP5K1A, PHOSPHO1 NAMPT 4669/4885PDK4 208/4885GRM1 906/4885
US-20250145609-A1 3-SUBSTITUTED PYRIDAZINE COMPOUNDS AS SMARCA2 AND/OR SMARCA4 DEGRADERS SMARCC1, SMARCC2, SMARCA4 NAMPT 2684/4885PDK4 892/4885GRM1 2741/4885
US-12559492-B2 BRAF degraders BRAF, NRAS, HRAS NAMPT 4414/4885PDK4 4425/4885GRM1 1349/4885
US-20260124309-A1 STAT6 DEGRADERS AND USES THEREOF STAT6, NCOR2, NCOR1 NAMPT 2432/4885PDK4 2483/4885GRM1 782/4885
US-20070032469-A1 Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators GRM2, GRM1, GRIN2B NAMPT 3926/4885PDK4 1921/4885GRM1 2/4885
US-20040044008-A1 Use of therapeutic benzamide derivatives MTTP, LIPC, CETP NAMPT 396/4885PDK4 714/4885GRM1 3933/4885
US-12479849-B2 EGFR inhibitors for the treatment of cancer EGFR, ERBB2, ERBB3 NAMPT 3852/4885PDK4 1976/4885GRM1 1061/4885
US-12570650-B2 6-substituted pyridazine compounds as SMARCA2 and/or SMARCA4 degraders SMARCC1, SMARCC2, SMARCA1 NAMPT 4646/4885PDK4 1939/4885GRM1 2753/4885

“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.