Phenylalanine

Phenylalanine

SCHEMBL1675272

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

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3PDE3APDE3BPDE4APDE4BPDE4CPDE4D

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
▸ ADORA3 known ✓ P0DMS8 1/20 0.51
▸ 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 0.61
▸ LTA4H P09960 1/20 0.57
▸ CYP1A2 P05177 1/20 0.53
▸ GRIA2 P42262 1/20 0.53
▸ CPA1 P15085 2/20 0.52
▸ CPB1 P15086 1/20 0.52
▸ CPA3 P15088 1/20 0.52
▸ CPB2 Q96IY4 1/20 0.52
▸ KDM4E B2RXH2 1/20 0.51
▸ USP2 O75604 1/20 0.51
▸ EGFR P00533 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 SCHEMBL1637917 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL4862934 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL1011892 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
D-Phenylalanine SCHEMBL1537448 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL3496164 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL2679075 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL9650016 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Phenylalanine SCHEMBL218898 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL21816915 1.00 SLC7A5 (0.85) SLC7A5PTGS1ALPIPKMXIAP
Dl-Phenylalanine SCHEMBL27579186 1.00 SLC7A5 (0.85) 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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102670428-A Preparation method and applications for cyclodextrin collagen tripeptide inclusion complex water solution UNIV FUDAN 2012-09-19 — — CN claimed
EP-0173233-B1 CHROMATOGRAPHIC METHOD AND MEANS PURDUE RESEARCH FOUNDATION (US) 1989-01-18 — — EP claimed
EP-0173233-A2 Chromatographic method and means PURDUE RESEARCH FOUNDATION (US) 1986-03-05 — — EP claimed
US-4544485-A HYDROPHOBIC COATING ON INNER SURFACES, HYDROPHILIC COATINGS ON OUTER SURFACES; SMALL PORE SIZE PURDUE RESEARCH FOUNDATION (US) 1985-10-01 — — US claimed
US-4340592-A OLICOPEPTIDES FOR DIETARY PURPOSES ADIBI SIAMAK A 1982-07-20 — — US claimed
US-20230014151-A1 COMBINATION ANTIVIRAL THERAPY FOR MEASLES CORNELL UNIVERSITY 2023-01-19 — — US disclosed
EP-4025586-A2 COMBINATION ANTIVIRAL THERAPY FOR MEASLES The Trustees of Columbia University in the City of New York (US) 2022-07-13 — — EP disclosed
WO-2021046398-A2 COMBINATION ANTIVIRAL THERAPY FOR MEASLES THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2021-03-11 — — WO disclosed
CN-107811996-A New type water-solubility tanshinone IIA polypeptide hydrogel nanometer medicine-carried system 中国药科大学 2018-03-20 — — CN disclosed
CN-107488209-A Gelator and its hydrogel prepare and application 四川大学 2017-12-19 — — CN disclosed
US-9006170-B2 Compositions for elastogenesis and connective tissue treatment HUMAN MATRIX SCIENCES, LLC (US) 2015-04-14 — — US disclosed
US-8871707-B2 Elastin producing fibroblast formulations and methods of using the same HUMAN MATRIX SCIENCES, LLC (US) 2014-10-28 — — US disclosed
WO-2004037848-A2 PROCESS FOR DETERMINING TARGET FUNCTION AND IDENTIFYING DRUG LEADS SLANETZ ALFRED E (US) 2004-05-06 — — WO disclosed
EP-1344060-A2 PROCESS FOR DETERMINING TARGET FUNCTION AND IDENTIFYING DRUG LEADS Slanetz, Alfred E. (US) 2003-09-17 — — EP disclosed
WO-2002058533-A2 PROCESS FOR DETERMINING TARGET FUNCTION AND IDENTIFYING DRUG LEADS SLANETZ ALFRED E (US) 2002-08-01 — — WO disclosed
US-20020046966-A1 Use of support materials in capillary electrochromatography EVOTEC BIOSYSTEMS AG (DE) 2002-04-25 — — US disclosed
US-5164090-A Separation of hydrophobic material, glass beads, controlled pore size E. R. SQUIBB & SONS, INC. (US) 1992-11-17 — — US disclosed
EP-0173233-B1 CHROMATOGRAPHIC METHOD AND MEANS PURDUE RESEARCH FOUNDATION (US) 1989-01-18 — — EP disclosed
EP-0173233-A2 Chromatographic method and means PURDUE RESEARCH FOUNDATION (US) 1986-03-05 — — EP disclosed
US-4544485-A HYDROPHOBIC COATING ON INNER SURFACES, HYDROPHILIC COATINGS ON OUTER SURFACES; SMALL PORE SIZE PURDUE RESEARCH FOUNDATION (US) 1985-10-01 — — 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-20230014151-A1 COMBINATION ANTIVIRAL THERAPY FOR MEASLES HM13, LRPPRC, TFRC ADORA3 4161/4885SLC7A5 2450/4885PTGS1 4770/4885

“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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