Glutamic Acid

Glutamic Acid

SCHEMBL5017170

CS(=O)(=O)O.N[C@@H](CCC(=O)O)C(=O)O

nearest known ligand 0.75

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Glutamic Acid. 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
GRIN2D known ✓ O15399 1/20 0.75
GRIN3B known ✓ O60391 1/20 0.75
GRIN1 known ✓ Q05586 1/20 0.75
GRIN2A known ✓ Q12879 1/20 0.75
GRIN2B known ✓ Q13224 1/20 0.75
GRIN2C known ✓ Q14957 1/20 0.75
GRIN3A known ✓ Q8TCU5 1/20 0.75
GRM8 O00222 2/20 0.75
GRM6 O15303 2/20 0.75
GRM7 Q14831 2/20 0.75
GRM4 Q14833 2/20 0.75
CYP1A2 P05177 2/20 0.75
GSR P00390 1/20 0.75
GRIK1 P39086 1/20 0.75
GRM5 P41594 1/20 0.75
GRIA1 P42261 1/20 0.75
GRIA2 P42262 1/20 0.75
GRIA3 P42263 1/20 0.75
SLC1A3 P43003 1/20 0.75
SLC1A2 P43004 1/20 0.75

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
D-Glutamate SCHEMBL5017167 1.00 GRM8 (0.75) GRM8GRM6GRM7GRM4CYP1A2
Glutamic Acid SCHEMBL1667361 0.91 GRM8 (0.82) GRM8GRM6GRM7GRM4CYP1A2
D-Glutamate SCHEMBL28742738 0.91 GRM8 (0.82) GRM8GRM6GRM7GRM4CYP1A2
D-Glutamate SCHEMBL1667360 0.91 GRM8 (0.82) GRM8GRM6GRM7GRM4CYP1A2
D-Glutamate SCHEMBL29060279 0.90 GRM8 (0.72) GRM8GRM6GRM7GRM4CYP1A2
Glutamic Acid SCHEMBL29259695 0.89 GRM8 (0.78) GRM8GRM6GRM7GRM4CYP1A2
D-Glutamate SCHEMBL29259696 0.89 GRM8 (0.78) GRM8GRM6GRM7GRM4CYP1A2
Glutamic Acid SCHEMBL5692202 0.89 GRM8 (0.78) GRM8GRM6GRM7GRM4CYP1A2
Glutamic Acid SCHEMBL28070258 0.89 GRM8 (0.78) GRM8GRM6GRM7GRM4CYP1A2
D-Glutamate SCHEMBL5691701 0.89 GRM8 (0.78) GRM8GRM6GRM7GRM4CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7078564-B2 Process for the preparation of ωbenzyl esters of amino diacids and of alkanesulphonates of these esters, and these alkanesulphonates ISOCHEM (FR) 2006-07-18 US claimed
US-20040133033-A1 Process for the preparation of omega-benzyl esters of amino diacids and of alkanesulphonates of these esters, and these alkanesulphonates ISOCHEM (FR) 2004-07-08 US claimed
CN-110023315-A Novel compound or pharmacologically acceptable salt thereof 国立研究开发法人理化学研究所 2019-07-16 CN disclosed
US-20180256717-A1 PROTEIN COMPOSITIONS AND USE THEREOF DRUG DISCOVERY LABORATORY AS (NO) 2018-09-13 US disclosed
EP-3236942-A1 PROTEIN COMPOSITIONS AND USE THEREOF Drug Discovery Laboratory AS (NO) 2017-11-01 EP disclosed
WO-2016103034-A1 PROTEIN COMPOSITIONS AND USE THEREOF DRUG DISCOVERY LABORATORY AS (NO) 2016-06-30 WO disclosed
US-7399860-B2 Manufacture of polyglutamate-therapeutic agent conjugates CELL THERAPEUTICS INC. (US) 2008-07-15 US disclosed
US-7078564-B2 Process for the preparation of ωbenzyl esters of amino diacids and of alkanesulphonates of these esters, and these alkanesulphonates ISOCHEM (FR) 2006-07-18 US disclosed
EP-1466627-A1 Polyglutamate camptothecin conjugates CELL THERAPEUTICS, INC. (US) 2004-10-13 EP disclosed
US-20040133033-A1 Process for the preparation of omega-benzyl esters of amino diacids and of alkanesulphonates of these esters, and these alkanesulphonates ISOCHEM (FR) 2004-07-08 US disclosed
US-20030224971-A1 Manufacture of polyglutamate-therapeutic agent conjugates CELL THERAPEUTICS, INC. 2003-12-04 US disclosed
EP-0952157-B1 9A, 11B-Dehydro derivatives of 9-oxime-3-keto-6-0-methylerythromycin PFIZER PROD INC (US) 2003-06-18 EP disclosed
US-20030054977-A1 Manufacture of polyglutamate-therapeutic agent conjugates CELL THERAPEUTICS, INC. 2003-03-20 US disclosed
EP-1225917-A2 MANUFACTURE OF POLYGLUTAMATE-THERAPEUTIC AGENT CONJUGATES CELL THERAPEUTICS, INC. (US) 2002-07-31 EP disclosed
US-20020077279-A1 Manufacture of polyglutamate-therapeutic agent conjugates KUMAR ANIL M (US) 2002-06-20 US disclosed
WO-2001026693-A2 MANUFACTURE OF POLYGLUTAMATE-THERAPEUTIC AGENT CONJUGATES CELL THERAPEUTICS, INC. (US) 2001-04-19 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 (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-20040133033-A1 Process for the preparation of omega-benzyl esters of amino diacids and of alkanesulphonates of these esters, and these alkanesulphonates ADH1C, DRD1, ABHD6 GRIN2D 636/4885GRIN3B 3393/4885GRIN1 1623/4885

“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.