SCHEMBL214944

SCHEMBL214944

CC(C)(C)OC(=O)N1CCN(c2ccc(N)c(N)c2)CC1

nearest known ligand 0.62

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.62
ALDH1A1 P00352 1/20 0.62
LMNA P02545 1/20 0.62
PDK2 Q15119 1/20 0.54
GPR119 Q8TDV5 8/20 0.52
SMARCA2 P51531 1/20 0.52
SMARCA4 P51532 1/20 0.52
PBRM1 Q86U86 1/20 0.52
SMN1; SMN2 Q16637 3/20 0.51
MEN1 O00255 3/20 0.51
KMT2A Q03164 3/20 0.51
NAMPT P43490 1/20 0.51
TSHR P16473 1/20 0.51
CYP2C19 P33261 1/20 0.49
HTT P42858 1/20 0.48
NPSR1 Q6W5P4 1/20 0.48
PIK3CA P42336 1/20 0.47

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
SCHEMBL30565931 1.00 MAPT (0.62) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL3613205 0.95 MAPT (0.57) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL214913 0.89 MAPT (0.60) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL470199 0.89 MAPT (0.56) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL29803690 0.89 MAPT (0.60) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL31130013 0.89 MAPT (0.56) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL31130014 0.89 MAPT (0.56) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL4722818 0.89 MAPT (0.60) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL7242118 0.88 MAPT (0.56) MAPTALDH1A1LMNAPDK2GPR119
SCHEMBL20352117 0.88 MAPT (0.55) MAPTALDH1A1LMNAPDK2GPR119

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3200589-B1 NOVEL 5-HYDROXYTRYPTAMINE RECEPTOR 7 ACTIVITY MODULATORS AND THEIR METHOD OF USE UNIV TEMPLE (US) 2026-03-11 EP disclosed
EP-4674484-A2 THIENOPYRROLE COMPOUNDS Gilead Sciences, Inc. (US) 2026-01-07 EP disclosed
EP-4291562-B1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES INC (US) 2025-09-10 EP disclosed
US-12365681-B2 Dihydrobenzimidazolones for medical treatment C4 THERAPEUTICS, INC. (US) 2025-07-22 US disclosed
WO-2025108255-A1 POLYCYCLIC DERIVATIVE, AND PREPARATION METHOD THEREFOR AND USE THEREOF 上海齐鲁制药研究中心有限公司 2025-05-30 WO disclosed
US-12286424-B2 Small molecule inhibitors of galectin-3 BRISTOL-MYERS SQUIBB COMPANY (US) 2025-04-29 US disclosed
US-12269809-B2 5-hydroxytryptamine receptor 7 activity modulators and their method of use TEMPLE UNIVERSITY-OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2025-04-08 US disclosed
CN-118344358-A HPK1 inhibitor and preparation method and application thereof 中国科学院上海有机化学研究所 2024-07-16 CN disclosed
US-20240217990-A1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES, INC. 2024-07-04 US disclosed
CN-118206529-A Dihydrobenzimidazolone C4医药公司 2024-06-18 CN disclosed
WO-2014121062-A1 SELECTIVE HDAC3 INHIBITORS ACETYLON PHARMACEUTICALS, INC. (US) 2014-08-07 WO disclosed
WO-2014121062-A1 SELECTIVE HDAC3 INHIBITORS ACETYLON PHARMACEUTICALS, INC. (US) 2014-08-07 WO disclosed
US-8088767-B2 JAK-2 modulators and methods of use EXELIXIS, INC. (US) 2012-01-03 US disclosed
US-8088767-B2 JAK-2 modulators and methods of use EXELIXIS, INC. (US) 2012-01-03 US disclosed
US-20100136136-A1 JAK-2 Modulators and Methods of Use EXELIXIS, INC. (US) 2010-06-03 US disclosed
US-20100136136-A1 JAK-2 Modulators and Methods of Use EXELIXIS, INC. (US) 2010-06-03 US disclosed
EP-2061768-A2 IMIDAZOLE-4,5-DICARBOXAMIDE DERIVATIVES AS JAK-2 MODULATORS Exelixis, Inc. (US) 2009-05-27 EP disclosed
WO-2008042282-A2 IMIDAZOLE-4, 5-DICARBOXAMIDE DERIVATIVES AS JAK-2 MODULATORS EXELIXIS, INC. (US) 2008-04-10 WO disclosed
WO-2008042282-A2 IMIDAZOLE-4, 5-DICARBOXAMIDE DERIVATIVES AS JAK-2 MODULATORS EXELIXIS, INC. (US) 2008-04-10 WO disclosed
US-6069143-A Fibrinogen receptor antagonists SMITHKLINE BEECHAM CORPORATION (US) 2000-05-30 US 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 (5 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-20100136136-A1 JAK-2 Modulators and Methods of Use JAK2, JAK1, JAK3 MAPT 2138/4885ALDH1A1 4295/4885LMNA 4821/4885
US-12286424-B2 Small molecule inhibitors of galectin-3 LGALS3, LGALS1, LGALS3BP MAPT 3151/4885ALDH1A1 2713/4885LMNA 1394/4885
US-12365681-B2 Dihydrobenzimidazolones for medical treatment CRBN, CUL4A, ADRM1 MAPT 2761/4885ALDH1A1 2009/4885LMNA 3835/4885
US-20240217990-A1 THIENOPYRROLE COMPOUNDS SSB, TPMT, LCP2 MAPT 3260/4885ALDH1A1 2343/4885LMNA 1961/4885
US-12269809-B2 5-hydroxytryptamine receptor 7 activity modulators and their method of use HTR7, HTR5A, HTR6 MAPT 1051/4885ALDH1A1 2423/4885LMNA 2675/4885

“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.