Homophenylalanine

Homophenylalanine

SCHEMBL1318113

NCC(=O)O.N[C@@H](CCc1ccccc1)C(=O)O

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3PDE3APDE3BPDE4APDE4BPDE4CPDE4D

The experimentally established mechanism targets of Homophenylalanine. 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
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
GRIK1 P39086 3/20 0.55
ERAP1 Q9NZ08 3/20 0.50
ANPEP P15144 2/20 0.50
ERAP2 Q6P179 2/20 0.50
KIF11 P52732 4/20 0.49
SLC1A3 P43003 1/20 0.49
SLC1A2 P43004 1/20 0.49
SLC1A1 P43005 1/20 0.49
GRIA1 P42261 1/20 0.48
GRIA2 P42262 1/20 0.48
GRIA3 P42263 1/20 0.48
GRIA4 P48058 1/20 0.48
GRIK2 Q13002 1/20 0.48
GRIK3 Q13003 1/20 0.48
CNR2 P34972 1/20 0.47

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
Homophenylalanine SCHEMBL44312 0.93 ALPI (0.64) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL130567 0.93 ALPI (0.64) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL44311 0.93 ALPI (0.64) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL1078733 0.93 ALPI (0.64) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL28594537 0.91 ALPI (0.62) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL28287974 0.91 ALPI (0.62) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL2305748 0.91 ALPI (0.62) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL28286602 0.91 ALPI (0.62) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL1245414 0.91 ALPI (0.62) ALPIPKMPTGS1XIAPSLC7A5
Homophenylalanine SCHEMBL1026468 0.91 ALPI (0.62) ALPIPKMPTGS1XIAPSLC7A5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10912839-B2 Methods of treating cancer using compounds containing a vascular disrupting agent ELLIPSES PHARMA LIMITED (GB) 2021-02-09 US disclosed
US-20200316212-A1 METHODS OF TREATING CANCER USING COMPOUNDS CONTAINING A VASCULAR DISRUPTING AGENT ELLIPSES PHARMA LTD (GB) 2020-10-08 US disclosed
US-10556014-B2 Compounds containing a vascular disrupting agent ELLIPSES PHARMA LIMITED (GB) 2020-02-11 US disclosed
US-10201622-B2 Tumour-targeted theranostic THE TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2019-02-12 US disclosed
EP-2349344-B1 MMP ACTIVATED VASCULAR DISRUPTING AGENTS INCANTHERA LTD (GB) 2018-12-05 EP disclosed
EP-3348282-A1 MMP ACTIVATED VASCULAR DISRUPTING AGENTS Incanthera Limited (GB) 2018-07-18 EP disclosed
US-20180177886-A1 Methods Of Treating Cancer Using Compounds Containing A Vascular Disrupting Agent ELLIPSES PHARMA LIMITED (GB) 2018-06-28 US disclosed
EP-2481429-B1 MMP-14 specific cleavage sequence INCANTHERA LTD (GB) 2018-05-09 EP disclosed
US-9956296-B2 Compounds containing a vascular disrupting agent INCANTHERA LTD (GB) 2018-05-01 US disclosed
US-9937267-B2 Methods of treating cancer using compounds containing a vascular disrupting agent INCANTHERA LTD (GB) 2018-04-10 US disclosed
US-8927486-B2 Compounds INCANTHERA LIMITED (GB) 2015-01-06 US disclosed
US-20140179592-A1 Compounds INCANTHERA LIMITED (GB) 2014-06-26 US disclosed
EP-2481429-A2 MMP Activated Vascular Disrupting Agents University of Bradford (GB) 2012-08-01 EP disclosed
EP-2481428-A2 MMP activated vascular disrupting agents University of Bradford (GB) 2012-08-01 EP disclosed
US-20110275554-A1 COMPOUNDS THE UNIVERSITY OF BRADFORD (GB) 2011-11-10 US disclosed
EP-2349344-A1 COMPOUNDS University of Bradford (GB) 2011-08-03 EP disclosed
US-20100168036-A1 GROWTH FACTOR UNIVERSITY OF BRADFORD (GB) 2010-07-01 US disclosed
WO-2010046628-A1 COMPOUNDS UNIVERSITY OF BRADFORD (GB) 2010-04-29 WO disclosed
EP-2134372-A2 MMP ACTIVATED VASCULAR DISRUPTING AGENTS University of Bradford (GB) 2009-12-23 EP disclosed
WO-2008125800-A2 MMP ACTIVATED VASCULAR DISRUPTING AGENTS UNIVERSITY OF BRADFORD (GB) 2008-10-23 WO 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 (7 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-20200316212-A1 METHODS OF TREATING CANCER USING COMPOUNDS CONTAINING A VASCULAR DISRUPTING AGENT MMP10, MMP25, MMP26 ALPI 1062/4885PKM 2526/4885PTGS1 386/4885
US-20110275554-A1 COMPOUNDS ADAM17, MMP3, MMP25 ALPI 2147/4885PKM 2732/4885PTGS1 562/4885
US-10912839-B2 Methods of treating cancer using compounds containing a vascular disrupting agent MMP10, MMP25, MMP26 ALPI 1062/4885PKM 2526/4885PTGS1 386/4885
US-20100168036-A1 GROWTH FACTOR HDGF, VEGFA, PGF ALPI 1570/4885PKM 4229/4885PTGS1 283/4885
US-20180177886-A1 Methods Of Treating Cancer Using Compounds Containing A Vascular Disrupting Agent MMP10, MMP25, MMP26 ALPI 1062/4885PKM 2526/4885PTGS1 386/4885
US-20140179592-A1 Compounds MMP9, MMP3, MMP10 ALPI 983/4885PKM 2760/4885PTGS1 580/4885
US-10556014-B2 Compounds containing a vascular disrupting agent MMP10, MMP11, MMP3 ALPI 1556/4885PKM 3322/4885PTGS1 359/4885

“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.