SCHEMBL7946364

SCHEMBL7946364

Oc1ccccc1CN1CCCCC1

nearest known ligand 0.81

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MPO P05164 2/20 0.81
KDM4E B2RXH2 4/20 0.76
HRH3 Q9Y5N1 1/20 0.65
ALDH1A1 P00352 3/20 0.61
TSHR P16473 1/20 0.59
GFER P55789 1/20 0.59
ACHE P22303 2/20 0.56
CYP2C19 P33261 1/20 0.54
HIF1A Q16665 1/20 0.54
CACNA1B Q00975 1/20 0.54
POLB P06746 1/20 0.53
LMNA P02545 2/20 0.53
HTT P42858 1/20 0.53
MAPK1 P28482 1/20 0.53
FAAH O00519 1/20 0.53
JAK2 O60674 1/20 0.51
RAB9A P51151 1/20 0.51
CRHBP P24387 1/20 0.51
CRHR2 Q13324 1/20 0.51
BRD4 O60885 1/20 0.51

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
SCHEMBL10415354 0.98 MPO (0.84) MPOKDM4EHRH3ALDH1A1TSHR
SCHEMBL3967782 0.90 MPO (1.00) MPOKDM4EHRH3ALDH1A1TSHR
Phosphoric Acid SCHEMBL28973467 0.89 MPO (0.70) MPOKDM4EHRH3ALDH1A1TSHR
SCHEMBL11194277 0.85 ALDH1A1 (0.73) MPOKDM4EHRH3ALDH1A1TSHR
SCHEMBL9388542 0.84 MPO (0.88) MPOKDM4EHRH3ALDH1A1TSHR
SCHEMBL26682722 0.83 MPO (0.66) MPOKDM4EHRH3ACHELMNA
SCHEMBL11196594 0.83 ALDH1A1 (0.69) MPOKDM4EHRH3ALDH1A1POLB
SCHEMBL10665335 0.82 KDM4E (0.70) MPOKDM4EHRH3ALDH1A1TSHR
SCHEMBL6573503 0.81 HRH3 (0.96) MPOKDM4EHRH3ALDH1A1GAA
SCHEMBL28290127 0.81 MPO (0.58) MPOKDM4EHRH3ALDH1A1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113588361-A Isoelectric point standard substance for free flow electrophoresis 上海蓝析生物技术有限公司 2021-11-02 CN claimed
CN-102395557-A Kinase inhibitor compounds UNIV FLORIDA 2012-03-28 CN claimed
CN-116693469-B Synthesis and refining method of roxatidine acetate hydrochloride 四川汇宇制药股份有限公司 2025-05-13 CN disclosed
CN-116693469-A Synthesis and refining method of roxatidine acetate hydrochloride 四川汇宇制药股份有限公司 2023-09-05 CN disclosed
CN-113588361-A Isoelectric point standard substance for free flow electrophoresis 上海蓝析生物技术有限公司 2021-11-02 CN disclosed
CN-107857743-B Method for preparing roxatidine acetate hydrochloride and intermediate 北京四环制药有限公司 2020-08-18 CN disclosed
EP-2764052-B1 IRON(III) CONTAINING COMPLEX AND CONDENSATION REACTION CATALYSTS, METHODS FOR PREPARING THE CATALYSTS, AND COMPOSITIONS CONTAINING THE CATALYSTS DOW SILICONES CORP (US) 2018-07-18 EP disclosed
US-9328205-B2 Iron(III) containing complex and condensation reaction catalysts, methods for preparing the catalysts, and compositions containing the catalysts DOW CORNING CORPORATION (US) 2016-05-03 US disclosed
US-20140371056-A1 Iron(III) Containing Complex and Condensation Reaction Catalysts, Methods for Preparing the Catalysts, and Compositions Containing the Catalysts DOW COMING CORPORATION (US) 2014-12-18 US disclosed
CN-102056933-B Thiazolopyridin-2-yloxy-phenyl and thiazolopyrazin-2-yloxy-phenyl amines as modulators of leukotriene A4 hydrolase JANSSEN PHARMACEUTICA NV 2014-09-17 CN disclosed
EP-2764052-A2 IRON(III) CONTAINING COMPLEX AND CONDENSATION REACTION CATALYSTS, METHODS FOR PREPARING THE CATALYSTS, AND COMPOSITIONS CONTAINING THE CATALYSTS Dow Corning Corporation (US) 2014-08-13 EP disclosed
CN-1305852-C Diaryl ethers as opioid receptor antagonists LILLY CO ELI (US) 2007-03-21 CN disclosed
CN-1681498-A Diaryl ethers as opioid receptor antagonist LILLY CO ELI (US) 2005-10-12 CN disclosed
US-6262078-B1 Phenoxymethyl piperidine derivatives for the treatment of neuropathic pain SYNTEX (U.S.A.) LLC 2001-07-17 US disclosed
US-6110937-A A SODIUM CHANNEL BLOCKER TREATING AS LOCAL ANESTHETICS AND IN THE TREATMENT OF CARDIAC ARRHYTHMIAS SYNTEX USA, INC. (US) 2000-08-29 US disclosed
EP-0869119-A1 Phenoxymethyl piperidine derivatives being sodium channle blockers F. HOFFMANN-LA ROCHE AG (CH) 1998-10-07 EP disclosed
CN-1194977-A Phenoxymethyl piperidine derivatives HOFFMANN LA ROCHE (CH) 1998-10-07 CN disclosed
EP-0325268-A1 1,4-Disubstituted-piperidinyl compounds MERRELL DOW PHARMACEUTICALS INC. (US) 1989-07-26 EP disclosed
US-4124545-A Carbamic acid esters as catalysts for trimerization of isocyanates BAYER AKTIENGESELLSCHAFT (DE) 1978-11-07 US disclosed
US-3985789-A Carbamic acid esters BAYER AKTIENGESELLSCHAFT (DT) 1976-10-12 US disclosed