Glutamic Acid

Glutamic Acid

SCHEMBL7294273

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

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRB1CDK4CDK6CHRM2CHRM3DPP4DRD2DRD3DRD4EGFRHRH1HTR1BHTR1DHTR1FHTR2AHTR2CHTR4SLC6A2SLC6A4

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
GRM8 O00222 2/20 0.95
GRM6 O15303 2/20 0.95
GRM7 Q14831 2/20 0.95
GRM4 Q14833 2/20 0.95
GSR P00390 2/20 0.95
GRIN2D O15399 1/20 0.95
GRIN3B O60391 1/20 0.95
CYP1A2 P05177 1/20 0.95
GRIK1 P39086 1/20 0.95
GRM5 P41594 1/20 0.95
GRIA1 P42261 1/20 0.95
GRIA2 P42262 1/20 0.95
GRIA3 P42263 1/20 0.95
SLC1A3 P43003 1/20 0.95
SLC1A2 P43004 1/20 0.95
SLC1A1 P43005 1/20 0.95
GRIA4 P48058 1/20 0.95
GRIN1 Q05586 1/20 0.95
GRIN2A Q12879 1/20 0.95
GRIK2 Q13002 1/20 0.95

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
Glutamic Acid SCHEMBL31507089 1.00 GRM8 (0.95) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL28296939 1.00 GRM8 (0.95) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL7294270 1.00 GRM8 (0.95) GRM8GRM6GRM7GRM4GSR
Glutamic Acid SCHEMBL7564767 0.97 GRM8 (0.90) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL1332297 0.97 GRM8 (1.00) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL1330484 0.97 GRM8 (1.00) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL410241 0.97 GRM8 (1.00) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL17127348 0.97 GRM8 (1.00) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL1330824 0.97 GRM8 (1.00) GRM8GRM6GRM7GRM4GSR
D-Glutamate SCHEMBL2201 0.97 GRM8 (1.00) GRM8GRM6GRM7GRM4GSR

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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-104685058-B Microorganisms and methods for making 4-hydroxybutyrate, 1, 4-butanediol, and related compounds 基因组股份公司 2020-07-07 CN claimed
US-20190284282-A1 STABLE PHARMACEUTICAL COMPOSITION DR. REDDY'S LABORATORIES LIMITED (IN) 2019-09-19 US claimed
EP-3402470-A1 STABLE PHARMACEUTICAL COMPOSITION Dr. Reddy's Laboratories Limited (IN) 2018-11-21 EP claimed
CN-108778261-A Stable pharmaceutical composition 雷迪博士实验室有限公司 2018-11-09 CN claimed
WO-2017122121-A1 STABLE PHARMACEUTICAL COMPOSITION DR. REDDY'S LABORATORIES LIMITED (IN) 2017-07-20 WO claimed
US-11713705-B2 Nitrous oxide removal catalysts for exhaust systems BASF CORPORATION (US) 2023-08-01 US disclosed
US-20220010714-A1 NITROUS OXIDE REMOVAL CATALYSTS FOR EXHAUST SYSTEMS BASF MOBILE EMISSIONS CATALYSTS LLC 2022-01-13 US disclosed
EP-3244995-B1 NITROUS OXIDE REMOVAL CATALYSTS FOR EXHAUST SYSTEMS BASF CORP (US) 2021-11-03 EP disclosed
US-11149610-B2 Nitrous oxide removal catalysts for exhaust systems BASF CORPORATION (US) 2021-10-19 US disclosed
US-20200232366-A1 NITROUS OXIDE REMOVAL CATALYSTS FOR EXHAUST SYSTEMS BASF MOBILE EMISSIONS CATALYSTS LLC 2020-07-23 US disclosed
CN-104685058-B Microorganisms and methods for making 4-hydroxybutyrate, 1, 4-butanediol, and related compounds 基因组股份公司 2020-07-07 CN disclosed
US-10634030-B2 Nitrous oxide removal catalysts for exhaust systems BASF CORPORATION (US) 2020-04-28 US disclosed
EP-2460539-A1 NANOSPHERE OR MICROSPHERE DRUG CARRIER, PREPARATION METHOD, COMPOSITION AND USE THEREOF Xi'an Libang Medical Technology Co., Ltd. (CN) 2012-06-06 EP disclosed
EP-1092766-A1 MICROORGANISM BELONGING TO THE GENUS CITROBACTER AND PROCESS FOR PRODUCING SHIKIMIC ACID TORAY INDUSTRIES, INC. (JP) 2001-04-18 EP disclosed
EP-0679084-A4 1995-11-08 EP disclosed
EP-0679084-A1 HYDANTOIN AND SUCCINIMIDE-SUBSTITUTED DERIVATIVES OF SPIROINDANYLCAMPHORSULFONYL OXYTOCIN ANTAGONISTS MERCK & CO. INC. (US) 1995-11-02 EP disclosed
WO-1994014438-A1 HYDANTOIN AND SUCCINIMIDE-SUBSTITUTED DERIVATIVES OF SPIROINDANYLCAMPHORSULFONYL OXYTOCIN ANTAGONISTS MERCK & CO., INC. (US) 1994-07-07 WO disclosed
US-5137904-A Useful in the treatment of atherosclerosis and thrombosis G. D. SEARLE & CO. (US) 1992-08-11 US disclosed
EP-0486280-A2 Piperidinylcamphorsulfonyl oxytocin antagonists MERCK & CO. INC. (US) 1992-05-20 EP disclosed
WO-1992007821-A1 DIASTEREOISOMERS OF BICYCLO-SUBSTITUTED PHENYLACETONITRILE DERIVATIVES G.D. SEARLE & CO. (US) 1992-05-14 WO disclosed