Glycine

Glycine

SCHEMBL28107196

Cl.NCC(=O)O.[Br-].[Na+]

nearest known ligand 0.00

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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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL28107246 0.96
Glycine SCHEMBL28019925 0.92
Glycine SCHEMBL4357419 0.92
Glycine SCHEMBL8201410 0.92
Glycine SCHEMBL6357710 0.92 GLRA1 (0.91)
Glycine SCHEMBL28861283 0.92 GLRA1 (0.91)
Glycine SCHEMBL11056979 0.92 GLRA1 (0.91)
Glycine SCHEMBL433424 0.92
Glycine SCHEMBL30898297 0.92
Glycine SCHEMBL5053459 0.92

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105985245-B Preparation method of salvianolic acid A through chemical conversion 中国科学院上海药物研究所 2024-06-07 CN disclosed
CN-105985245-A Chemical conversion preparing method for salvianolic acid A 中国科学院上海药物研究所 2016-10-05 CN disclosed