Phenylalanine

Phenylalanine

SCHEMBL246543

N[C@@H](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 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
Dl-Phenylalanine SCHEMBL246542 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 41 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260034169-A1 STABILISED SILICIC ACID SOLUTIONS BARLAA B.V. (NL) 2026-02-05 US disclosed
EP-4565530-A1 STABILISED SILICIC ACID SOLUTIONS Barlaa B.V. (NL) 2025-06-11 EP disclosed
CN-119894823-A Stable silicic acid solutions 巴尔拉有限公司 2025-04-25 CN disclosed
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
WO-2024028039-A1 STABILISED SILICIC ACID SOLUTIONS BARLAA B.V. (NL) 2024-02-08 WO 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-102698808-B The purposes of a kind of composite catalyst and clean catalytic oxidization cyclohexene synthesizing adipic acid thereof BEIJING XUYANG CHEMICAL TECHNOLOGY RESEARCH INSTITUTE CO., LTD. (CN) 2015-07-29 CN disclosed
EP-2330124-B1 Hybrid polypeptides with selectable properties AMYLIN PHARMACEUTICALS LLC (US) 2015-02-25 EP disclosed
WO-2002094873-A2 PREPARATION OF CHOLECYSTOKININ AGONISTS AND ANTAGONISTS, AND THEIR THERAPEUTIC AND DIAGNOSTIC USE BRACCO IMAGING S.P.A. (IT) 2002-11-28 WO disclosed
US-20020102256-A1 Peptide and polypeptide inhibitors of complement C1s ZYMOGENETICS, INC. 2002-08-01 US disclosed
WO-2001098365-A2 PEPTIDE AND POLYPEPTIDE INHIBITORS OF COMPLEMENT C1S ZYMOGENETICS, INC. (US) 2001-12-27 WO disclosed
US-5723576-A POLYPEPTIDES FOR ENZYME INHIBITORS AND HIRUNDIN DEVELOPMENT BIOTECHNOLOGICAL PROCESSES S.N.C. (IT) 1998-03-03 US 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-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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20260034169-A1 STABILISED SILICIC ACID SOLUTIONS HAO2, SMS, SSTR2 SLC7A5 14/4885PTGS1 1633/4885ALPI 2144/4885
US-20020102256-A1 Peptide and polypeptide inhibitors of complement C1s C1S, C1QBP, C1R SLC7A5 3648/4885PTGS1 2655/4885ALPI 3020/4885

“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.