SCHEMBL2006303

SCHEMBL2006303

CC(C)(C)OC(=O)N1CCC(Cl)CC1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 1/20 0.65
RECQL P46063 1/20 0.61
EPHX1 P07099 1/20 0.57
USP2 O75604 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
PTPN2 P17706 1/20 0.55
PTPN1 P18031 1/20 0.55
PTPN6 P29350 1/20 0.55
GPR119 Q8TDV5 4/20 0.53
MAPT P10636 2/20 0.51
KDM4E B2RXH2 1/20 0.51
THRB P10828 1/20 0.51
STS P08842 4/20 0.51
KMT2A Q03164 1/20 0.50
ALDH1A1 P00352 2/20 0.49
NPC1 O15118 1/20 0.48
MAPK1 P28482 1/20 0.48
HTT P42858 1/20 0.48
RAB9A P51151 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48

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
SCHEMBL20893369 0.89 HPGD (0.53) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL1712246 0.87 HPGD (0.64) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL28195249 0.86 HPGD (0.68) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL696090 0.86 HPGD (0.62) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL310117 0.86 GPR119 (0.67) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL11904378 0.85 HPGD (0.66) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL2015039 0.85 HPGD (0.66) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL12321125 0.85 HPGD (0.66) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL43357 0.85 HPGD (0.66) HPGDRECQLEPHX1USP2SMN1; SMN2
SCHEMBL26608596 0.85 HPGD (0.66) 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 39 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118063455-A Method for preparing Ruimei pam intermediate 尚科生物医药(上海)有限公司 2024-05-24 CN claimed
CN-102659668-B Method for synthesizing 1-alkyl-piperidine-4-sulfonyl benzylamine SUZHOU HANDE CHUANGHONG BIOCHEMICAL TECHNOLOGY CO LTD 2014-04-09 CN claimed
CN-102659668-A Method for synthesizing 1-alkyl-piperidine-4-sulfonyl benzylamine SUZHOU HANDE CHUANGHONG BIOCHEMICAL TECHNOLOGY CO LTD 2012-09-12 CN claimed
US-12351924-B2 Electroreductive cross coupling OHIO STATE INNOVATION FOUNDATION (US) 2025-07-08 US disclosed
WO-2025111513-A1 COMPOUNDS USEFUL IN THE MODULATION OF KLHDC1 AND KLHDC2 ACTIVITY NURIX THERAPEUTICS, INC. (US) 2025-05-30 WO disclosed
US-20240254136-A1 COMPOUNDS TARGETING RNA-BINDING PROTEINS OR RNA-MODIFYING PROTEINS Redona Therapeutics, Inc. 2024-08-01 US disclosed
WO-2024123967-A1 SARM1 INHIBITORS, PHARMACEUTICAL COMPOSITIONS, AND THERAPEUTIC APPLICATIONS SENYA PHARMACEUTICALS, INC. (US) 2024-06-13 WO disclosed
CN-115677569-B Synthesis method of pyridines and substituted benzenes based on reduction coupling reaction of iron-catalyzed aryl halide and alkyl halide 重庆大学 2024-05-28 CN disclosed
CN-118063455-A Method for preparing Ruimei pam intermediate 尚科生物医药(上海)有限公司 2024-05-24 CN disclosed
US-20230250539-A1 ELECTROREDUCTIVE CROSS COUPLING OHIO STATE INNOVATION FOUNDATION 2023-08-10 US disclosed
CN-116157392-A Compounds targeting RNA binding proteins or RNA modification proteins 雷多纳治疗公司 2023-05-23 CN disclosed
US-20080275069-A1 Quinazoline Derivative MSD K.K. (JP) 2008-11-06 US disclosed
EP-1987020-A1 AZACYCLYL-SUBSTITUTED ARYLDIHYDROISOQUINOLINONES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS Sanofi-Aventis (FR) 2008-11-05 EP disclosed
WO-2007093364-A1 AZACYCLYL-SUBSTITUTED ARYLDIHYDROISOQUINOLINONES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS SANOFI-AVENTIS (DE) 2007-08-23 WO disclosed
US-20070167453-A1 Nitrogenous fused heteroaromatic ring derivative MSD K.K. (JP) 2007-07-19 US disclosed
EP-1757594-A1 QUINAZOLINE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-02-28 EP disclosed
CN-1922183-A Nitrogenous fused heteroaromatic ring derivative BANYU PHARMA CO LTD (JP) 2007-02-28 CN disclosed
EP-1719756-A1 NITROGENOUS FUSED HETEROAROMATIC RING DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2006-11-08 EP disclosed
US-5670511-A Indolepiperidine derivatives MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1997-09-23 US disclosed
EP-0722942-A1 Indole piperidine derivatives MERCK PATENT GmbH (DE) 1996-07-24 EP 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 (3 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-20080275069-A1 Quinazoline Derivative HRH3, HRH4, HRH2 HPGD 1054/4885RECQL 596/4885EPHX1 2791/4885
US-20070167453-A1 Nitrogenous fused heteroaromatic ring derivative HRH3, HRH2, HRH4 HPGD 573/4885RECQL 3050/4885EPHX1 850/4885
US-20240254136-A1 COMPOUNDS TARGETING RNA-BINDING PROTEINS OR RNA-MODIFYING PROTEINS NSUN3, NSUN2, RBM3 HPGD 4835/4885RECQL 1027/4885EPHX1 4735/4885

“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.