Glycine

Glycine

SCHEMBL4201161

NCC(=O)O.Oc1cc2cc-2c1O

nearest known ligand 0.42

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3PDE3APDE3BPDE4APDE4BPDE4CPDE4D

The experimentally established mechanism targets of Glycine. 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
▸ GLRA1 P23415 1/20 0.42
▸ SLC6A9 P48067 1/20 0.42
▸ OR51E2 Q9H255 1/20 0.42
▸ TDP1 Q9NUW8 6/20 0.37
▸ KDM4E B2RXH2 5/20 0.37
▸ MAPT P10636 5/20 0.37
▸ HSD17B10 Q99714 4/20 0.37
▸ ALDH1A1 P00352 3/20 0.37
▸ LMNA P02545 3/20 0.37
▸ HPGD P15428 3/20 0.37
▸ MAPK1 P28482 2/20 0.37
▸ CA12 O43570 1/20 0.37
▸ CA1 P00915 1/20 0.37
▸ CA2 P00918 1/20 0.37
▸ TP53 P04637 1/20 0.37
▸ CA3 P07451 1/20 0.37
▸ SELL P14151 1/20 0.37
▸ SELP P16109 1/20 0.37
▸ FUT4 P22083 1/20 0.37
▸ CA4 P22748 1/20 0.37

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
Acetic Acid SCHEMBL7570296 0.80 KDM4E (0.41) TDP1KDM4EMAPTHSD17B10ALDH1A1
Acetamide SCHEMBL7546231 0.78 LMNA (0.36) TDP1KDM4EMAPTHSD17B10ALDH1A1
Glycine SCHEMBL5386703 0.75 BACE1 (0.44) GLRA1SLC6A9OR51E2TDP1KDM4E
Glycine SCHEMBL5077295 0.73 FFAR4 (0.44) GLRA1SLC6A9OR51E2CA1CA2
Gallic Acid SCHEMBL4126178 0.72 KDM4E (0.74) GLRA1SLC6A9OR51E2TDP1KDM4E
Phloroglucinol SCHEMBL28571198 0.69 GLRA1 (0.59) GLRA1SLC6A9OR51E2LMNACA12
Glycine SCHEMBL30338272 0.68 GLRA1 (0.91) GLRA1SLC6A9OR51E2KDM4EALDH1A1
Glycine SCHEMBL30338545 0.68 GLRA1 (0.91) GLRA1SLC6A9OR51E2KDM4EALDH1A1
Glycine SCHEMBL29906512 0.68 — —
Glycine SCHEMBL252376 0.66 GLRA1 (0.62) GLRA1SLC6A9OR51E2MAPTLMNA

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107952065-A Include the Insulin Aspart for being substituted anionic compound 阿道恰公司 2018-04-24 — — CN claimed
CN-104902922-B Fast acting insulin formulations comprising substituted anionic compounds 阿道恰公司 2017-12-12 — — CN claimed
US-8883716-B2 Method for treating damaged tissue of the CNS MEDTRONIC, INC. (US) 2014-11-11 — — US disclosed
US-20120143272-A1 METHOD FOR TREATING DAMAGED TISSUE OF THE CNS MEDTRONIC, INC. (US) 2012-06-07 — — US disclosed
EP-2027120-A2 MGLUR5 MODULATORS I AstraZeneca AB (SE) 2009-02-25 — — EP disclosed
EP-1919901-A1 SUBSTITUTED PIPERAZINES AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS AstraZeneca AB (SE) 2008-05-14 — — EP disclosed
WO-2007130820-A2 MGLUR5 MODULATORS I ASTRAZENECA AB (SE) 2007-11-15 — — WO disclosed
WO-2007021573-A1 SUBSTITUTED PIPERAZINES AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS ASTRAZENECA AB (SE) 2007-02-22 — — WO disclosed
US-20050123526-A1 Administration of growth factors for neurogenesis and gliagenesis MEDTRONIC INC. (US) 2005-06-09 — — US disclosed
EP-1536790-A2 OXADIAZOLES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR-5 AstraZeneca AB (SE) 2005-06-08 — — EP disclosed
WO-2004014370-A2 OXADIAZOLES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR-5 ASTRAZENECA AB (SE) 2004-02-19 — — WO disclosed
JP-2003335666-A MEDICAMENT FOR SPECIFICALLY INHIBITING NEUROCYTE IN HYPERSTIMULATION KATO NOBUO 2003-11-25 — — JP disclosed
WO-2002068417-A3 HETEROPOLYCYCLIC COMPOUNDS AND THEIR USE AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS SLASSI ABDELMALIK (CA) 2002-11-14 — — WO disclosed
EP-1255735-A2 PYRIDINE DERIVATIVES AS POTENTIATORS OF GLUTAMATE RECEPTORS ELI LILLY AND COMPANY (US) 2002-11-13 — — EP disclosed
WO-2001056990-A2 PYRIDINE DERIVATES AS POTENTIATORS OF GLUTAMATE RECEPTORS ELI LILLY AND COMPANY (US) 2001-08-09 — — WO disclosed
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