Dl-Phenylalanine

Dl-Phenylalanine

SCHEMBL288606

NC(Cc1ccccc1)C(=O)O.N[C@@H](Cc1ccccc1)C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SLC7A5 Q01650 4/20 1.00
▸ PTGS1 P23219 2/20 1.00
▸ ALPI P09923 1/20 1.00
▸ PKM P14618 1/20 1.00
▸ XIAP P98170 1/20 1.00
▸ SLC1A3 P43003 2/20 0.69
▸ SLC1A2 P43004 2/20 0.69
▸ SLC1A1 P43005 2/20 0.69
▸ SLC15A1 P46059 1/20 0.63
▸ CYP1A2 P05177 1/20 0.61
▸ LTA4H P09960 1/20 0.59
▸ GRIA2 P42262 1/20 0.59
▸ KDM4E B2RXH2 1/20 0.58
▸ USP2 O75604 1/20 0.58
▸ EGFR P00533 1/20 0.58
▸ LCK P06239 1/20 0.58
▸ FYN P06241 1/20 0.58
▸ ADORA3 P0DMS8 1/20 0.58
▸ ALOX15 P16050 1/20 0.58
▸ HTR2A P28223 1/20 0.58

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 SCHEMBL1331077 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL1449128 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL1332173 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL1331829 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL8835931 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
SCHEMBL23159186 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL1331777 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL2785094 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL1330932 1.00 SLC7A5 (1.00) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL1331205 1.00 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 31 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1261623-B1 NEW RETINOL DERIVATIVES, THE METHOD OF PREPARATIONS AND THE USES THEREOF CHEBIGEN INC (KR) 2009-11-04 — — EP claimed
EP-0652229-A2 Oligopeptides with fungicidal activity ISAGRO S.p.A. (IT) 1995-05-10 — — EP claimed
WO-2022213201-A1 APPARATUS AND METHODOLOGIES FOR DETECTION, DIAGNOSIS, AND PROGNOSIS OF BRAIN INJURY UTI LIMITED PARTNERSHIP (CA) 2022-10-13 — — WO disclosed
WO-2016183093-A1 INHIBITORS OF VIRUSES UNIVERSITY OF KANSAS (US) 2016-11-17 — — WO disclosed
EP-2449488-A1 METHOD FOR NORMALIZATION IN METABOLOMICS ANALYSIS METHODS WITH ENDOGENOUS REFERENCE METABOLITES BIOCRATES Life Sciences AG (AT) 2012-05-09 — — EP disclosed
EP-2427773-A1 METHOD OF DIAGNOSING ASPHYXIA Keller, Matthias (DE) 2012-03-14 — — EP disclosed
CN-101497655-B Polypeptide hydration salt compound and use for anti-depression aspect BEIJING YUANSEN KANGTAI MEDICINE CO LTD 2011-11-23 — — CN disclosed
US-20110275708-A1 POLYCYCLIC COMPOUNDS AND METHODS RELATED THERETO CORNELL UNIVERSITY (US) 2011-11-10 — — US disclosed
CN-1973037-B Process for producing dipeptide or dipeptide derivative KYOWA HAKKO KOGYO KK 2011-10-19 — — CN disclosed
US-7989434-B2 Heterocyclic self-immolative linkers and conjugates SEATTLE GENETICS, INC. (US) 2011-08-02 — — US disclosed
WO-2011000753-A1 METHOD FOR NORMALIZATION IN METABOLOMICS ANALYSIS METHODS WITH ENDOGENOUS REFERENCE METABOLITES BIOCRATES LIFE SCIENCES AG (AT) 2011-01-06 — — WO disclosed
CN-1286535-C Adsorbent for eliminating hepatitis C virus, adsorber, and adsorption method KANEKA CORP (JP) 2006-11-29 — — CN disclosed
US-20050256030-A1 for linking drug moieties to ligands; comprises a peptide sequence that is a substrate for an intracellular enzyme, for example a cathepsin, that cleaves the peptide at an amide bond SEAGEN INC. 2005-11-17 — — US disclosed
CN-1420793-A Absorbents for dilated cardiomyopathy KANEKA CORP (JP) 2003-05-28 — — CN disclosed
CN-1407993-A Gene recombinant antibody and its fragment KYOWA HAKKO KOGYO KK (JP) 2003-04-02 — — CN disclosed
EP-0624377-B1 Lysosomal enzyme-cleavable antitumor drug conjugates BRISTOL MYERS SQUIBB CO (US) 2002-01-23 — — EP disclosed
US-6214345-B1 ANTITUMOR AGENTS; DRUG CONJUGATES WHICH ARE SELECTIVELY ACTIVATIBLE AT THE SITE OF THE TUMOR BRISTOL-MYERS SQUIBB CO. 2001-04-10 — — US disclosed
CN-1251048-A Adsorbent, adsorber and adsorption method for eliminating hepatitis C virus KANEKA CORP (JP) 2000-04-19 — — CN disclosed
CN-1100426-A Lysosomal enzyme-cleavable antitumor drug conjugates BRISTOL MYERS SQUIBB CO (US) 1995-03-22 — — CN disclosed
EP-0624377-A2 Lysosomal enzyme-cleavable antitumor drug conjugates Bristol-Myers Squibb Company (US) 1994-11-17 — — 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-20050256030-A1 for linking drug moieties to ligands; comprises a peptide sequence that is a substrate for an intracellular enzyme, for example a cathepsin, that cleaves the peptide at an amide bond CTSS, CTSE, CTSL SLC7A5 510/4885PTGS1 4140/4885ALPI 2563/4885
US-20110275708-A1 POLYCYCLIC COMPOUNDS AND METHODS RELATED THERETO PKD1, THPO, CCNO SLC7A5 2579/4885PTGS1 34/4885ALPI 290/4885

“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.

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