SCHEMBL5153023

SCHEMBL5153023

C=CCC(O)c1ccc(Br)cc1

nearest known ligand 0.48

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
HRH3 Q9Y5N1 1/20 0.44
CYP2C19 P33261 2/20 0.43
IGF1R P08069 7/20 0.39
HMOX1 P09601 1/20 0.39
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
SLC18A3 Q16572 2/20 0.37
CXCR3 P49682 1/20 0.37
HTR2A P28223 1/20 0.36
PYCR1 P32322 1/20 0.36
SIGMAR1 Q99720 1/20 0.36
CYP1A2 P05177 1/20 0.35

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
SCHEMBL13662800 1.00 HRH3 (0.44) HRH3CYP2C19IGF1RHMOX1MEN1
SCHEMBL15184685 1.00 HRH3 (0.44) HRH3CYP2C19IGF1RHMOX1MEN1
Acetic Acid SCHEMBL28854263 0.89 CYP1A2 (0.44) HRH3CYP2C19IGF1RMEN1KMT2A
SCHEMBL10457217 0.83 TAAR1 (0.54) HRH3CYP2C19CYP1A2
SCHEMBL2690630 0.82 CYP2C19 (0.40) CYP2C19IGF1RHMOX1MEN1KMT2A
SCHEMBL15184752 0.81 AOC3 (0.47) HRH3CYP2C19
SCHEMBL867450 0.81 AOC3 (0.47) HRH3CYP2C19
SCHEMBL21353855 0.81 AOC3 (0.47) HRH3CYP2C19IGF1RMEN1KMT2A
SCHEMBL7104502 0.81 AOC3 (0.47) HRH3CYP2C19IGF1RMEN1KMT2A
SCHEMBL3245046 0.81 HRH3 (0.43) HRH3CYP2C19

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117486836-A Preparation method of 2-aryl-3-carbonyl substituted tetrahydrofuran and tetrahydropyran compound 遵义医科大学 2024-02-02 CN disclosed
CN-104450852-B A kind of preparation method of homoallylic alcohol class compound 宁夏大学 2018-01-09 CN disclosed
CN-104478936-B The preparation and application of bi triphenyl antimony organic (V) title complex of a kind of ionic 湖南大学 2016-06-08 CN disclosed
CN-104478936-A Preparation method and application of ionic type bis-triphenyl organic antimony (V) complex UNIV HUNAN 2015-04-01 CN disclosed
CN-104450852-A Method for preparing homoallylic alcohol compound UNIV NINGXIA 2015-03-25 CN disclosed
US-7314943-B2 Pyran derivatives containing an exocyclic double bond MERCK PATENT GMBH (DE) 2008-01-01 US disclosed
US-7314943-B2 Pyran derivatives containing an exocyclic double bond MERCK PATENT GMBH (DE) 2008-01-01 US disclosed
EP-1515945-A4 METHOD FOR MAKING ARYL HYDRAZINES AND SUBSTITUTED INDOLES RHODIA PHARMA SOLUTION INC FOR (US) 2007-07-18 EP disclosed
EP-1515945-A2 METHOD FOR MAKING ARYL HYDRAZINES AND SUBSTITUTED INDOLES Rhodia Pharma Solution Inc., (formally Rhodia Chirex Inc.) (US) 2005-03-23 EP disclosed
WO-2004000218-A2 METHOD FOR MAKING ARYL HYDRAZINES AND SUBSTITUTED INDOLES RHODIA PHARMA SOLUTIONS INC., (FORMALLY RHODIA CHIREX INC.) (US) 2003-12-31 WO disclosed
US-6489512-B1 REACTING AROMATIC COMPOUND BEARING ACTIVATED CARBON ATOM AND HYDRAZONE IN PRESENCE OF TRANSITION METAL CATALYST TO FORM ARYL HYDRAZONE, HYDROLYZING TO FORM ARYL HYDRAZINE, CYCLIZING IN PRESENCE OF ACID CATALYST TO FORM SUBSTITUTED INDOLE RHODIA CHIREX INC. 2002-12-03 US disclosed