SCHEMBL6456079

SCHEMBL6456079

CC(C)(C)OC(=O)N1CCC(C#CCO)CC1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 1/20 0.49
RECQL P46063 1/20 0.47
EPHX1 P07099 1/20 0.47
USP2 O75604 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
ALDH1A1 P00352 2/20 0.44
GPR119 Q8TDV5 3/20 0.44
NR1H2 P55055 1/20 0.43
MAPT P10636 2/20 0.43
NPC1 O15118 1/20 0.43
MAPK1 P28482 1/20 0.43
HTT P42858 1/20 0.43
RAB9A P51151 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
KDM4E B2RXH2 1/20 0.43
THRB P10828 1/20 0.43
PTPN2 P17706 1/20 0.43
PTPN1 P18031 1/20 0.43
PTPN6 P29350 1/20 0.43
DPP4 P27487 1/20 0.43

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
SCHEMBL25256802 0.91 ALDH1A1 (0.46) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL6450266 0.88 HPGD (0.47) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL27120710 0.87 HPGD (0.48) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL21405187 0.85 GPR119 (0.47) HPGDRECQLEPHX1GPR119NR1H2
SCHEMBL21405190 0.85 GPR119 (0.47) HPGDRECQLEPHX1GPR119NR1H2
SCHEMBL25301539 0.84 NR1H2 (0.53) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL25301424 0.83 MEN1 (0.53) HPGDEPHX1ALDH1A1NR1H2MAPT
SCHEMBL12820311 0.83 HPGD (0.53) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL6446543 0.82 GPR119 (0.44) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL15203221 0.81 HPGD (0.51) HPGDRECQLEPHX1USP2SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115232108-B SOS1 degradation agent and preparation method and application thereof 领泰生物医药(绍兴)有限公司 2025-04-18 CN disclosed
EP-4463450-A1 FUSED HETEROARYL HYDROXAMATES AS STING AGONISTS Bisichem Co., Ltd. (KR) 2024-11-20 EP disclosed
CN-118510770-A Fused heteroaryl hydroxamic acids as STING agonists 比西切姆有限公司 2024-08-16 CN disclosed
CN-114945560-B GPR119 agonists 卡尔优普公司 2024-08-13 CN disclosed
US-20240261417-A1 SOS1 DEGRADING AGENT AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF LEADINGTAC PHARMACEUTICAL (SHAOXING) CO., LTD. (CN) 2024-08-08 US disclosed
US-20240261418-A1 SOS1 DEGRADING AGENT AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF LEADINGTAC PHARMACEUTICAL (SHAOXING) CO., LTD. (CN) 2024-08-08 US disclosed
US-20240217983-A1 GPR119 AGONISTS KALLYOPE, INC. 2024-07-04 US disclosed
CN-118076595-A Five-membered and six-membered compound, preparation method, pharmaceutical composition and application 杭州多域生物技术有限公司 2024-05-24 CN disclosed
EP-4328219-A1 SOS1 DEGRADING AGENT AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF Shanghai Leadingtac Pharmaceutical Co. Ltd. (CN) 2024-02-28 EP disclosed
EP-4320129-A1 GPR119 AGONISTS Kallyope, Inc. (US) 2024-02-14 EP disclosed
US-9006228-B2 Substituted cyclopropyl compounds, compositions containing such compounds, and methods of treatment MERCK SHARP & DOHME CORP. (US) 2015-04-14 US disclosed
US-9006228-B2 Substituted cyclopropyl compounds, compositions containing such compounds, and methods of treatment MERCK SHARP & DOHME CORP. (US) 2015-04-14 US disclosed
US-9006228-B2 Substituted cyclopropyl compounds, compositions containing such compounds, and methods of treatment MERCK SHARP & DOHME CORP. (US) 2015-04-14 US disclosed
US-20140128368-A1 SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT MERCK SHARP & DOHME CORP. (US) 2014-05-08 US disclosed
US-20140128368-A1 SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT MERCK SHARP & DOHME CORP. (US) 2014-05-08 US disclosed
US-20140128368-A1 SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT MERCK SHARP & DOHME CORP. (US) 2014-05-08 US disclosed
US-6964974-B2 2,3-oxidosqualene-lanosterol cyclase inhibitors HOFFMANN-LA ROCHE INC. (US) 2005-11-15 US disclosed
EP-1317432-A1 PIPERIDINE DERIVATIVES FOR USE AS 2,3-OXIDOSQUALENE-LANOSTEROL CYCLASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2003-06-11 EP disclosed
US-20020068753-A1 2,3-oxidosqualene-lanosterol cyclase inhibitors HOFFMANN-LA ROCHE INC. 2002-06-06 US disclosed
WO-2002020483-A1 PIPERIDINE DERIVATIVES FOR USE 2,3-OXIDOSQUALENE-LANOSTEROL CYCLASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2002-03-14 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 (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-20240261418-A1 SOS1 DEGRADING AGENT AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF SOS1, RAC1, RSU1 HPGD 3600/4885RECQL 1329/4885EPHX1 544/4885
US-20240217983-A1 GPR119 AGONISTS GPR119, GLP1R, GCGR HPGD 1594/4885RECQL 4620/4885EPHX1 1614/4885
US-20140128368-A1 SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT GPR119, GCGR, GPR27 HPGD 940/4885RECQL 3133/4885EPHX1 1614/4885
US-20240261417-A1 SOS1 DEGRADING AGENT AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF RAC1, SOS1, RSU1 HPGD 2612/4885RECQL 1447/4885EPHX1 474/4885
US-20020068753-A1 2,3-oxidosqualene-lanosterol cyclase inhibitors CYP51A1, LSS, CYP46A1 HPGD 43/4885RECQL 3404/4885EPHX1 2072/4885

“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.