SCHEMBL2245201

SCHEMBL2245201

C[C@@H]1CN(c2cccc(Cl)c2)CCN1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR3E A5X5Y0 2/20 0.61
HTR3B O95264 2/20 0.61
HTR3A P46098 2/20 0.61
HTR3D Q70Z44 2/20 0.61
HTR3C Q8WXA8 2/20 0.61
ADRB1 P08588 2/20 0.61
TP53 P04637 1/20 0.61
CYP1A2 P05177 1/20 0.61
CYP3A4 P08684 1/20 0.61
HTR1A P08908 1/20 0.61
CYP2D6 P10635 1/20 0.61
THRB P10828 1/20 0.61
CYP2C9 P11712 1/20 0.61
HTR2A P28223 1/20 0.61
HTR2C P28335 1/20 0.61
SLC6A4 P31645 1/20 0.61
CYP2C19 P33261 1/20 0.61
HTR7 P34969 1/20 0.61
HTR2B P41595 1/20 0.61
HTT P42858 1/20 0.61

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
SCHEMBL4240000 1.00 HTR3E (0.61) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL12892626 1.00 HTR3E (0.61) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL30208090 1.00 HTR3E (0.61) HTR3EHTR3BHTR3AHTR3DHTR3C
Hydrochloric Acid SCHEMBL20139242 0.98 HTR3E (0.59) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL5632352 0.83 ADRB1 (0.56) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL5632344 0.83 ADRB1 (0.56) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL30005135 0.83 ADRB1 (0.56) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL315161 0.83 ADRB1 (0.63) ADRB1NOTUMKHKALOX5MAPT
SCHEMBL8534451 0.82 ADRB1 (0.55) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL8109027 0.81 KHK (0.50) ADRB1KHKBCL2A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9062015-B2 Inhibitors of sphingosine kinase MERCK PATENT GMBH (DE) 2015-06-23 US disclosed
US-9062015-B2 Inhibitors of sphingosine kinase MERCK PATENT GMBH (DE) 2015-06-23 US disclosed
CN-1989106-B N-hydroxyamide derivatives and their use MERCK SERONO SA 2013-12-04 CN disclosed
US-20120252789-A1 INHIBITORS OF SPHINGOSINE KINASE MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 2012-10-04 US disclosed
US-8247437-B2 N-hydroxyamide derivatives and use thereof MERCK SERONO SA (CH) 2012-08-21 US disclosed
US-20110263628-A1 N-HYDROXYAMIDE DERIVATIVES AND USE THEREOF APPLIED RESEARCH SYSTEMS ARS HOLDING N.V. (AN) 2011-10-27 US disclosed
US-8008302-B2 ((2S,3S) N,2-dihydroxy-5-methyl-3-{[4-(2-pyridinyl)-1-piperazinyl]carbonyl}hexanamide; for treatment and/or prevention of disorders related to autoimmune disorders and/or inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, stroke, cancer, pre-term labor, endometriosis MERCK SERONO SA (CH) 2011-08-30 US disclosed
WO-2011072791-A1 SPHINGOSINE KINASE INHIBITORS MERCK PATENT GMBH (DE) 2011-06-23 WO disclosed
US-7879836-B2 treatment of hyperphagia comprising the administering 1-(3-chlorophenyl)-3-alkylpiperazine derivatives such as 1-(3-chlorophenyl)-3-ethylpiperazine; anorexigenic agents AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. (IT) 2011-02-01 US disclosed
US-7879836-B2 treatment of hyperphagia comprising the administering 1-(3-chlorophenyl)-3-alkylpiperazine derivatives such as 1-(3-chlorophenyl)-3-ethylpiperazine; anorexigenic agents AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. (IT) 2011-02-01 US disclosed
CN-1046281-C Pharmacologically active enantiomers and process for their preparation ANGELINI RICERCHE SPA (IT) 1999-11-10 CN disclosed
US-5973150-A PHARMACOLOGICAL PROFILE SIMILAR TO THAT OF TRAZODONE BUT ALSO HAVE SOME ADVANTAGES SUCH AS, FOR EXAMPLE, A REDUCED AFFINITY FOR ADRENERGIC RECEPTORS. ANGELINI RICERCHE S.P.A. SOCIETA' CONSORTILE (IT) 1999-10-26 US disclosed
CN-1215052-A Pharmacollogically active enantiomers and method for their preparation ANGELINI RICERCHE SPA (IT) 1999-04-28 CN disclosed
CN-1215053-A Pharmacologically active enantiomers and method for their preparation ANGELINI RICERCHE SPA (IT) 1999-04-28 CN disclosed
US-5817815-A 2-(3-(4-(3-CHLOROPHENYL)-1-(2-METHYL)-PIPERAZINYL)PROPYL)-1,2, 4-TRIAZOLO(4.3-A)PYRIDINE-3(2H)-ONE, ANALGESICS ANGELINI RICERCHE S.P.A. SOCIETA CONSORTILE (IT) 1998-10-06 US disclosed
US-5741907-A CYCLIZATION; SALT FORMATION; SEPARATION ANGELINI RICERCHE S.P.A. SOCIETA' CONSORTILE (IT) 1998-04-21 US disclosed
EP-0707587-B1 PHARMACOLOGICALLY ACTIVE ENANTIOMERS ANGELINI RICERCHE SPA (IT) 1997-10-01 EP disclosed
CN-1129939-A Pharmacologically active enantiomers ANGELINI FRANCESCO IST RICERCA (IT) 1996-08-28 CN disclosed
EP-0707587-A1 PHARMACOLOGICALLY ACTIVE ENANTIOMERS ANGELINI RICERCHE SPA (IT) 1996-04-24 EP disclosed
WO-1995001354-A1 PHARMACOLOGICALLY ACTIVE ENANTIOMERS ANGELINI RICERCHE S.P.A. SOCIETA' CONSORTILE (IT) 1995-01-12 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 (2 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-20110263628-A1 N-HYDROXYAMIDE DERIVATIVES AND USE THEREOF HNMT, HCAR2, HPGD HTR3E 497/4885HTR3B 307/4885HTR3A 305/4885
US-20120252789-A1 INHIBITORS OF SPHINGOSINE KINASE SPHK1, SPHK2, S1PR3 HTR3E 1908/4885HTR3B 1285/4885HTR3A 1454/4885

“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.