Phenethylamine

Phenethylamine

SCHEMBL5306641

N.NCCc1ccccc1

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

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 SCHEMBL31461079 0.97 HTR2A (0.89) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL11664723 0.97 HTR2A (0.89) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL27634208 0.97 HTR2A (1.00) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL1330939 0.97
Phenethylamine SCHEMBL968 0.97
Phenethylamine SCHEMBL1332244 0.97
Phenethylamine SCHEMBL1331271 0.97
Phenethylamine SCHEMBL1799333 0.97 HTR2A (1.00) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL8384113 0.94 HTR2A (0.94) HTR2ALOXL2TAAR1CYP2A6SMN1; SMN2
Phenethylamine SCHEMBL245154 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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102627571-A Preparation and synthesis method for chiral ammonium salt MEI LUO 2012-08-08 CN claimed
CN-113423436-B Microbiota metabolites that shape host physiology 耶鲁大学 2024-02-06 CN disclosed
CN-113437222-B Lead-free tin-based perovskite thin film, lead-free tin-based perovskite solar cell and preparation method thereof 西北工业大学 2023-09-08 CN disclosed
US-20230043198-A1 MICROBIOTA METABOLITES THAT SHAPE HOST PHYSIOLOGY YALE UNIVERSITY (US) 2023-02-09 US disclosed
EP-3893941-A1 MICROBIOTA METABOLITES THAT SHAPE HOST PHYSIOLOGY Yale University (US) 2021-10-20 EP disclosed
CN-113437222-A Lead-free tin-based perovskite thin film, lead-free tin-based perovskite solar cell and preparation method of lead-free tin-based perovskite solar cell 西北工业大学 2021-09-24 CN disclosed
CN-113423436-A Metabolites of microbial populations that shape host physiology 耶鲁大学 2021-09-21 CN disclosed
WO-2020123376-A1 MICROBIOTA METABOLITES THAT SHAPE HOST PHYSIOLOGY YALE UNIVERSITY (US) 2020-06-18 WO disclosed
WO-2020063216-A1 PEPTOID COMPOUND AND PREPARATION METHOD THEREFOR, OLIGOMER, PHARMACEUTICAL COMPOSITION AND KIT 京东方科技集团股份有限公司 2020-04-02 WO disclosed
US-20190298661-A1 Transdermal Delivery of Phenethylamine Monoamine Releasers THE CORPORATION OF MERCER UNIVERSITY 2019-10-03 US disclosed
US-6762052-B1 THE ENZYMES ARE USEFUL IN METABOLISM STUDIES, IN SCREENING OF COMPOUNDS FOR BIOLOGICAL OR PHARMACOLOGICAL ACTIVITY, AS WELL AS SERVING AS A BIO-INDICATOR OF DISEASE STATES OR SUSCEPTIBILITY TO DISEASE STATES CASHMAN JOHN R 2004-07-13 US disclosed
EP-1076649-A1 ISOQUINOLINE COMPOUND MELANOCORTIN RECEPTOR LIGANDS AND METHODS OF USING SAME TREGA BIOSCIENCES, INC. (US) 2001-02-21 EP disclosed
US-6127381-A A MELANOCORTIN RECEPTOR LIGAND FOR REGULATING FOOD INTAKE AND BODY WEIGHT, REGULATING CYTOKINE ACTIVITY, ANTI-INFLAMMATORY ACTIVITY LION BIOSCIENCE AG (DE) 2000-10-03 US disclosed
WO-1999055679-A1 ISOQUINOLINE COMPOUND MELANOCORTIN RECEPTOR LIGANDS AND METHODS OF USING SAME TREGA BIOSCIENCES, INC. (US) 1999-11-04 WO disclosed
EP-0434213-B1 Monosubstituted dithiooxamide compounds and their use MINNESOTA MINING & MFG (US) 1995-04-05 EP disclosed
US-5124308-A Reacts with transition metal salt for carbonless paper copying MINNESOTA MINING AND MANUFACTURING COMPANY 1992-06-23 US disclosed
US-5041654-A Transamination in wallach reaction; controlling temperature; reactant amine concentration MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1991-08-20 US disclosed
EP-0434213-A1 Monosubstituted dithiooxamide compounds and their use MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1991-06-26 EP disclosed
EP-0431783-A1 Preparation of monosubstituted dithiooxamide compounds MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1991-06-12 EP disclosed
US-4280958-A COPPER-TYPE CATALYST USED IN CYCLIZATION OF A HALOGENOPHENETHYLAMINE IN THE PRESENCE OF AN AMINE IHARA CHEMICAL INDUSTRY CO., LTD. (JP) 1981-07-28 US 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 (1 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-20190298661-A1 Transdermal Delivery of Phenethylamine Monoamine Releasers PNMT, TAAR5, QDPR HTR2A 62/4885LOXL2 4453/4885TAAR1 4/4885

“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.