Glycine

Glycine

SCHEMBL3882403

NCC(=O)O.NN(Cc1ccccc1)Cc1ccccc1

nearest known ligand 0.50

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
AOC3 Q16853 2/20 0.48
AKR1B1 P15121 1/20 0.46
NPC1 O15118 3/20 0.46
RAB9A P51151 3/20 0.46
CA12 O43570 1/20 0.46
CA9 Q16790 1/20 0.46
KDM4E B2RXH2 1/20 0.44
LMNA P02545 1/20 0.44
CA2 P00918 1/20 0.44
KEAP1 Q14145 1/20 0.43
ALDH1A1 P00352 2/20 0.43
NPSR1 Q6W5P4 1/20 0.43
CARM1 Q86X55 1/20 0.42
PRMT6 Q96LA8 1/20 0.42
PRMT8 Q9NR22 1/20 0.42
TSHR P16473 1/20 0.42
GLRA1 P23415 1/20 0.42
SLC6A9 P48067 1/20 0.42
OR51E2 Q9H255 1/20 0.42
GLA P06280 1/20 0.42

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
SCHEMBL833414 0.84 AOC3 (0.64) AOC3CA2ALDH1A1CARM1PRMT6
SCHEMBL1794281 0.84 AOC3 (0.64) AOC3CA2ALDH1A1CARM1PRMT6
SCHEMBL4622916 0.83 AOC3 (0.48) AOC3AKR1B1NPC1RAB9ACA12
Hydrochloric Acid SCHEMBL11779718 0.82 AOC3 (0.61) AOC3LMNACA2ALDH1A1CARM1
Acetic Acid SCHEMBL27673324 0.77 CARM1 (0.55) AOC3NPC1RAB9ACA12CA9
SCHEMBL258776 0.76 AOC3 (0.54) AOC3AKR1B1NPC1RAB9ACA12
SCHEMBL27718040 0.76 AOC3 (0.54) AOC3NPC1RAB9ACA12CA9
Phenylacetic Acid SCHEMBL28668840 0.76 AKR1B1 (0.81) AKR1B1LMNACA2TSHRHTT
SCHEMBL4210846 0.75 LMNA (0.53) AOC3NPC1RAB9AKDM4ELMNA
SCHEMBL17454767 0.74 MAOB (0.60) AOC3NPC1RAB9AKDM4ECA2

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
US-7504521-B2 Methods for the preparation of pyrrolotriazine compounds BRISTOL-MYERS SQUIBB CO. (US) 2009-03-17 US disclosed
US-20060030708-A1 Methods for the preparation of pyrrolotriazine compounds BRISTOL-MYERS SQUIBB COMPANY 2006-02-09 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-20060030708-A1 Methods for the preparation of pyrrolotriazine compounds SDHB, SDHA, DHPS AOC3 548/4885AKR1B1 1398/4885NPC1 2382/4885

“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.