L-Phenylalaninol

L-Phenylalaninol

SCHEMBL81769

N[C@H](CO)Cc1ccccc1

nearest known ligand 0.76

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.76
ANPEP P15144 2/20 0.64
SLC6A2 P23975 2/20 0.56
TAAR1 Q96RJ0 2/20 0.56
MAOA P21397 1/20 0.56
SLC6A4 P31645 1/20 0.56
SLC6A3 Q01959 1/20 0.56
SIGMAR1 Q99720 1/20 0.56
CYP2A6 P11509 1/20 0.56
ADORA2A P29274 1/20 0.56
ADORA1 P30542 1/20 0.56
ALPI P09923 1/20 0.56
PKM P14618 1/20 0.56
PTGS1 P23219 1/20 0.56
XIAP P98170 1/20 0.56
SLC7A5 Q01650 1/20 0.56
TRPA1 O75762 1/20 0.56
CYP2D6 P10635 1/20 0.52
LAP3 P28838 3/20 0.52
MMP2 P08253 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
L-Phenylalaninol SCHEMBL2521 1.00 EPHX1 (0.76) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL7422483 1.00 EPHX1 (0.76) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL177073 1.00 EPHX1 (0.76) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL87692 1.00 EPHX1 (0.76) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL31229492 0.98 EPHX1 (0.73) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL15467495 0.98 EPHX1 (0.73) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL7252746 0.98 EPHX1 (0.73) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL30996912 0.98 EPHX1 (0.73) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL27430394 0.98 EPHX1 (0.73) EPHX1ANPEPSLC6A2TAAR1MAOA
L-Phenylalaninol SCHEMBL27521331 0.98 EPHX1 (0.73) EPHX1ANPEPSLC6A2TAAR1MAOA

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

Appears in 3343 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260138972-A1 PREPARATION METHOD AND CHIRAL SIEVING APPLICATION OF NOVEL 12-CROWN-4 COVALENT ORGANIC FRAMEWORKS CHONGQING UNIV OF ARTS AND SCIENCES (CN) 2026-05-21 US claimed
US-12534571-B2 Amphiphilic block copolymer, preparation method thereof and nanomicelle drug-loading system SHANGHAI BEST-LINK BIOSCIENCE, LLC (CN) 2026-01-27 US claimed
WO-2025133248-A1 DIASTEREOMERIC AMINOALCOHOL AND AMINOETHER SALTS OF 2-[(4R,S)-8-FLUORO-2-[4-(3-METHOXYPHENYL)PIPERAZIN-1-YL]-3-[2-METHOXY-5-(TRIFLUOROMETHYL)PHENYL]-3,4-DIHYDROQUINAZOLIN-4-YL]ACETIC ACID AND THEIR USE FOR ENANTIOMERIC SEPARATION AIC246 AG & CO. KG (DE) 2025-06-26 WO claimed
CN-116640319-B Organic chiral supermolecular gel based on 1-naphthylmethyl amine and application thereof in chiral recognition 常州大学 2025-05-27 CN claimed
CN-120025542-A Non-isocyanate polyurethane and multicomponent selective synthesis method thereof 华南理工大学 2025-05-23 CN claimed
WO-2025104679-A1 PROCESSES FOR MAKING INTERMEDIATES FOR ISOINDOLINONE INHIBITORS OF THE MDM2-P53 INTERACTION HAVING ANTICANCER ACTIVITY OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2025-05-22 WO claimed
US-20250135005-A1 PROCESSES FOR PREPARING FUNCTIONALIZED CYCLOOCTENES TAMBO INC (US) 2025-05-01 US claimed
CN-119899373-A (-) -Gossypol derivative and preparation method thereof and antioxidant 武汉轻工大学 2025-04-29 CN claimed
CN-119823023-A Process for preparing functionalized cyclooctenes 坦博公司 2025-04-15 CN claimed
US-12234208-B2 3,4-dihydroxy-n-(1′-benzyl-2′-hydroxyethyl)-2-methylpyridine chloride, and synthesis and use thereof HANGZHOU ZEDE PHARMA-TECH CO. LTD. (CN) 2025-02-25 US claimed
EP-0449884-A4 DERIVATIVES OF TETRAPEPTIDES AS CCK AGONISTS 1991-10-30 EP claimed
EP-0449884-A1 DERIVATIVES OF TETRAPEPTIDES AS CCK AGONISTS ABBOTT LABORATORIES (US) 1991-10-09 EP claimed
WO-1991001370-A1 PROTECTION OF NK CELL CYTOLYTIC ACTIVITY IN PBMC E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-02-07 WO claimed
US-4978744-A Synthesis of dolastatin 10 ARIZONA BOARD OF REGENTS (US) 1990-12-18 US claimed
WO-1989010916-A1 ENANTIOSELECTIVE ADDITION OF HYDROCARBONS TO ALPHA,BETA-UNSATURATED CARBONYL COMPOUNDS MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1989-11-16 WO claimed
EP-0105696-B1 OPTICALLY ACTIVE N-SUBSTITUTED PHENYLALANINOLS AND USE THEREFOR Dainippon Pharmaceutical Co., Ltd. (JP) 1986-01-02 EP claimed
US-4536601-A USE FOR RESOLUTION OF D-3-ACETHYLTHIO-2-METHYLPROPIONIC ACID DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 1985-08-20 US claimed
EP-0124388-A1 Strain of Trichoderma harzianum, process for its isolation, process for its culture, peptides or compounds produced by this strain and application of this strain and these peptides or the product produced by the culture process as a means for biological control in the form of a phytosanitary product LES PRODUITS ORGANIQUES DU SANTERRE ORSAN (FR) 1984-11-07 EP claimed
EP-0105696-A1 Optically active N-substituted phenylalaninols and use therefor Dainippon Pharmaceutical Co., Ltd. (JP) 1984-04-18 EP claimed
US-4014895-A Method for synthesis of optically active thiolactones SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1977-03-29 US claimed