Glycine

Glycine

SCHEMBL9274191

NCC(=O)O.NCC(=O)O.O=P(O)(O)O

nearest known ligand 0.71

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 0.71
SLC6A9 P48067 1/20 0.71
OR51E2 Q9H255 1/20 0.71
LMNA P02545 6/20 0.47
BLM P54132 4/20 0.47
KMT2A Q03164 3/20 0.47
TSHR P16473 2/20 0.47
MEN1 O00255 2/20 0.47
HPGD P15428 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
GABRR1 P24046 4/20 0.43
ALDH1A1 P00352 2/20 0.40
THRB P10828 2/20 0.38
NPSR1 Q6W5P4 2/20 0.38
GABRR3 A8MPY1 1/20 0.38
GABRP O00591 1/20 0.38
GABRD O14764 1/20 0.38
HDAC3 O15379 1/20 0.38
GABBR2 O75899 1/20 0.38
CYP1A2 P05177 1/20 0.38

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
Glycine SCHEMBL29130842 1.00 GLRA1 (0.71) GLRA1SLC6A9OR51E2LMNABLM
Glycine SCHEMBL1023304 1.00 GLRA1 (0.71) GLRA1SLC6A9OR51E2LMNABLM
Glycine SCHEMBL28244367 0.97 GLRA1 (0.67) GLRA1SLC6A9OR51E2LMNABLM
Glycine SCHEMBL9637396 0.94 OR51E2 (0.62) GLRA1SLC6A9OR51E2LMNABLM
Succinic Acid SCHEMBL14881109 0.91 OR51E2 (0.59) GLRA1SLC6A9OR51E2LMNABLM
Glycine SCHEMBL25331208 0.88 GLRA1 (0.56) GLRA1SLC6A9OR51E2LMNABLM
Glycine SCHEMBL25333156 0.88 GLRA1 (0.56) GLRA1SLC6A9OR51E2LMNABLM
Glycine SCHEMBL11661976 0.87 GLRA1 (0.62) GLRA1SLC6A9OR51E2LMNABLM
Methyl Phosphonate SCHEMBL758011 0.87 GLRA1 (0.62) GLRA1SLC6A9OR51E2LMNABLM
Methyl Phosphonate SCHEMBL15419630 0.87 GLRA1 (0.62) GLRA1SLC6A9OR51E2LMNABLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0290047-B1 Dipyridoxyl phosphate nuclear magnetic resonance imagery contrast agents NYCOMED SALUTAR INC (US) 1995-02-01 EP disclosed
EP-0290041-B1 Radioactive metal chelates of dipyridoxyl phosphate NYCOMED SALUTAR INC (US) 1993-12-08 EP disclosed
US-5223243-A Dipyridoxyl phosphate chelating compound intermediates useful as NMRI contrast agents SALUTAR, INC. (US) 1993-06-29 US disclosed
US-5130431-A Chelate compound intermediates an NMR contrast agents SALUTAR, INC. (US) 1992-07-14 US disclosed
US-5091169-A Water soluble, stable chelates with paramagnetic metal ions SALUTAR, INC. (US) 1992-02-25 US disclosed
US-4992555-A Certain dipyridylphosphate chelatable compounds capable of forming metal ion chelates SALUTAR, INC. (US) 1991-02-12 US disclosed
US-4992554-A Used as contrast agent in nuclear magnetic resonance imagery SALUTAR, INC. (US) 1991-02-12 US disclosed
US-4933456-A STABLE, SOLUBLE SALUTAR, INC. (US) 1990-06-12 US disclosed
US-4842845-A Radioactive metal chelates for dipyridoxyl phosphate SALUTAR, INC. (US) 1989-06-27 US disclosed
EP-0290047-A2 Dipyridoxyl phosphate nuclear magnetic resonance imagery contrast agents NYCOMED SALUTAR, INC. (US) 1988-11-09 EP disclosed