Dl-Phenylalanine

Dl-Phenylalanine

SCHEMBL246542

NC(Cc1ccccc1)C(=O)O.O=S(=O)(O)O

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Dl-Phenylalanine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 4/20 0.85
PTGS1 P23219 2/20 0.85
ALPI P09923 1/20 0.85
PKM P14618 1/20 0.85
XIAP P98170 1/20 0.85
SLC1A3 P43003 2/20 0.61
SLC1A2 P43004 2/20 0.61
SLC1A1 P43005 2/20 0.61
SLC15A1 P46059 1/20 0.56
CYP1A2 P05177 1/20 0.53
LTA4H P09960 1/20 0.53
GRIA2 P42262 1/20 0.53
KDM4E B2RXH2 1/20 0.51
USP2 O75604 1/20 0.51
EGFR P00533 1/20 0.51
LCK P06239 1/20 0.51
FYN P06241 1/20 0.51
ADORA3 P0DMS8 1/20 0.51
ALOX15 P16050 1/20 0.51
HTR2A P28223 1/20 0.51

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
Dl-Phenylalanine SCHEMBL27873303 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL246543 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL11240666 0.98 SLC7A5 (0.81) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL8610376 0.93 SLC7A5 (0.79) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL8610372 0.93 SLC7A5 (0.79) SLC7A5PTGS1ALPIPKMXIAP
SCHEMBL23159186 0.92 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL8118 0.92 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL16398196 0.92 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL385804 0.92 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL8119 0.92 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101684076-B Process for preparing amides CHINA PETROCHEMICAL DEV CORP 2013-04-17 CN claimed
CN-102146051-B Method for separating amide from amino acid ionic liquid CHINA PETROCHEMICAL DEV CORP 2013-03-27 CN claimed
CN-102039179-B Catalytic composition for preparing amide and method for preparing amide CHINA PETROCHEMICAL DEV CORP 2013-03-06 CN claimed
CN-102146051-A Method for separating amide from amino acid ionic liquid CHINA PETROCHEMICAL DEV CORP 2011-08-10 CN claimed
CN-102039179-A Catalytic composition for preparing amide and method for preparing amide CHINA PETROCHEMICAL DEV CORP 2011-05-04 CN claimed
CN-101684076-A Process for preparing amides CHINA PETROCHEMICAL DEV CORP 2010-03-31 CN claimed
CN-113651959-B Nanometer medicine carrying system based on amino acid-hydroxy acid copolymer and preparation method and application thereof 中山大学 2024-05-07 CN disclosed
CN-114438566-B Aluminum product anodic oxidation liquid and use method thereof 四川大学 2024-02-23 CN disclosed
CN-114438566-A Aluminum material anodic oxidation liquid and use method thereof 四川大学 2022-05-06 CN disclosed
CN-112603908-B Nano drug-loading system based on amino acid polymer and preparation method and application thereof 中山大学 2022-02-08 CN disclosed
CN-113651959-A Nano drug loading system based on amino acid-hydroxy acid copolymer and preparation method and application thereof 中山大学 2021-11-16 CN disclosed
CN-112603908-A Nano drug-loading system based on amino acid polymer and preparation method and application thereof 中山大学 2021-04-06 CN disclosed
CN-108135944-A Probiotics and prebiotic compositions and its method and purposes for adjusting microorganism group 伊夫罗生物科学公司 2018-06-08 CN disclosed
EP-0376230-B1 Preparation and isolation of mineral acid salt of an amino methyl ester MITSUI TOATSU CHEMICALS (JP) 1994-11-23 EP disclosed
US-5113009-A PREPARATION AND ISOLATION OF MINERAL ACID SALT OF AN AMINO ACID METHYL ESTER MITSUI TOATSU CHEMICALS, INCORPORATED 1992-05-12 US disclosed
EP-0376230-A2 Preparation and isolation of mineral acid salt of an amino methyl ester MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-07-04 EP disclosed
EP-0057092-B1 PROCESS FOR RACEMIZING AN OPTICALLY ACTIVE ALPHA-AMINO ACID OR A SALT THEREOF Tanabe Seiyaku Co., Ltd. (JP) 1985-05-02 EP disclosed
US-4427762-A DEVELOPMENT WITH ALKALINE DEVELOPER MIXTURE KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1984-01-24 US disclosed
US-4401820-A IN THE PRESENCE OF AN ACYCLIC ACID AND AN ALDEHYDE; STABILITY TANABE SEIYAKU CO., LTD. (JP) 1983-08-30 US disclosed
EP-0057092-A1 Process for racemizing an optically active alpha-amino acid or a salt thereof Tanabe Seiyaku Co., Ltd. (JP) 1982-08-04 EP disclosed