Phenethylamine

Phenethylamine

SCHEMBL3932674

B.NCCc1ccccc1

nearest known ligand 0.94

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Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ HTR2A P28223 3/20 0.94
▸ LOXL2 Q9Y4K0 2/20 0.94
▸ TAAR1 Q96RJ0 2/20 0.94
▸ CYP2A6 P11509 1/20 0.94
▸ SMN1; SMN2 Q16637 1/20 0.94
▸ MAOA P21397 3/20 0.64
▸ MAOB P27338 3/20 0.59
▸ CYP1A2 P05177 1/20 0.58
▸ CYP2D6 P10635 1/20 0.58
▸ CYP2C19 P33261 1/20 0.58
▸ HTR6 P50406 2/20 0.56
▸ HTR2C P28335 1/20 0.54
▸ ALDH1A1 P00352 1/20 0.52
▸ HPGD P15428 1/20 0.52
▸ ALOX15 P16050 1/20 0.52
▸ ALOX12 P18054 1/20 0.52
▸ CASP1 P29466 1/20 0.52
▸ HSD17B10 Q99714 1/20 0.52

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
Phenethylamine SCHEMBL23093677 0.97 HTR2A (0.89) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL1332244 0.97 — —
Phenethylamine SCHEMBL27634208 0.97 HTR2A (1.00) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL968 0.97 — —
Phenethylamine SCHEMBL1330939 0.97 — —
Phenethylamine SCHEMBL1331271 0.97 — —
Phenethylamine SCHEMBL1799333 0.97 HTR2A (1.00) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL9650507 0.94 HTR2A (0.94) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL20568335 0.94 HTR2A (0.94) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL8384113 0.94 HTR2A (0.94) HTR2ALOXL2TAAR1CYP2A6SMN1; 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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090196821-A1 PLATED COBALT-BORON CATALYST ON HIGH SURFACE AREA TEMPLATES FOR HYDROGEN GENERATION FROM SODIUM BOROHYDRIDE UNIVERSITY OF DELAWARE (US) 2009-08-06 — — US disclosed
US-4923999-A Optically active borane complex and a method for producing an optically active alcohol derivative by the use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1990-05-08 — — US disclosed
EP-0142566-B1 ASYMMETRICALLY MODIFIED BORON HYDRIDE COMPOUNDS, PROCESS FOR ITS PREPARATION, AND PROCESS FOR PREPARING OPTICALLY ACTIVE ALCOHOL DERIVATIVE USING SAME SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1989-08-23 — — EP disclosed
EP-0171175-B1 AN OPTICALLY ACTIVE BORANE COMPLEX AND A METHOD FOR PRODUCING AN OPTICALLY ACTIVE ALCOHOL DERIVATIVE BY THE USE THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1989-05-24 — — EP disclosed
US-4749809-A Optically active borane complex and a method for producing an optically active alcohol derivative by the use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1988-06-07 — — US disclosed
EP-0171175-A1 An optically active borane complex and a method for producing an optically active alcohol derivative by the use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1986-02-12 — — EP disclosed
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