Aspartic Acid

Aspartic Acid

SCHEMBL3379838

N[C@@H](CC(=O)O)C(=O)O.O=P(O)(O)O

nearest known ligand 0.55

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Known targets — ChEMBL curated mechanism

SSTR1SSTR2SSTR3SSTR5

The experimentally established mechanism targets of Aspartic 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 0.48
GRM6 O15303 2/20 0.48
GRM7 Q14831 2/20 0.48
GRM4 Q14833 2/20 0.48
GRIK1 P39086 2/20 0.48
GRIK2 Q13002 2/20 0.48
GRM1 Q13255 2/20 0.48
GRM2 Q14416 2/20 0.48
FOLH1 Q04609 1/20 0.46
SLC7A5 Q01650 1/20 0.46
GRIN2D O15399 1/20 0.46
GRIN3B O60391 1/20 0.46
GSR P00390 1/20 0.46
CYP1A2 P05177 1/20 0.46
GRM5 P41594 1/20 0.46
GRIA1 P42261 1/20 0.46
GRIA2 P42262 1/20 0.46
GRIA3 P42263 1/20 0.46
SLC1A3 P43003 1/20 0.46
SLC1A2 P43004 1/20 0.46

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
Aspartic Acid SCHEMBL3379835 1.00 GRM8 (0.48) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL1891183 0.93 GRM8 (0.47) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL1891184 0.93 GRM8 (0.47) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL11300995 0.91 SLC7A5 (0.48) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL3231 0.89
D-Aspartate SCHEMBL145539 0.89
Aspartic Acid SCHEMBL1526976 0.89 GRIK1 (0.56) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL11065189 0.89 GRIK1 (0.56) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL11065185 0.89 GRIK1 (0.56) GRM8GRM6GRM7GRM4GRIK1
Aspartic Acid SCHEMBL996424 0.89 GRIK1 (0.56) GRM8GRM6GRM7GRM4GRIK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120040763-A Polyimide and polyvinyl alcohol composite material with random copolymerization and preparation method thereof 常州大学 2025-05-27 CN claimed
CN-117024801-A Preparation method of conductive flame-retardant double-property polyvinyl alcohol transparent film 安徽理工大学环境友好材料与职业健康研究院(芜湖) 2023-11-10 CN claimed
CN-120040763-A Polyimide and polyvinyl alcohol composite material with random copolymerization and preparation method thereof 常州大学 2025-05-27 CN disclosed
CN-118184831-A Carbomer carrier structure polymer formed by carbomer and phosphoric acid amino acid, and preparation and application thereof 吉林省远志医学科技有限公司 2024-06-14 CN disclosed
WO-2024011666-A1 L-HOMOSERINE HIGH-YIELD STRAIN, CONSTRUCTION METHOD THEREFOR, AND USE THEREOF 南京盛德生物科技研究院有限公司 2024-01-18 WO disclosed
CN-117024801-A Preparation method of conductive flame-retardant double-property polyvinyl alcohol transparent film 安徽理工大学环境友好材料与职业健康研究院(芜湖) 2023-11-10 CN disclosed
CN-117024801-A Preparation method of conductive flame-retardant double-property polyvinyl alcohol transparent film 安徽理工大学环境友好材料与职业健康研究院(芜湖) 2023-11-10 CN disclosed
CN-116286566-A L-homoserine high-yield strain and construction method and application thereof 南京盛德生物科技研究院有限公司 2023-06-23 CN disclosed
CN-115725537-A Aspartokinase mutant and application thereof in producing L-homoserine 中国科学院天津工业生物技术研究所 2023-03-03 CN disclosed
CN-111607551-B Method for producing aspartic acid, derivatives thereof and glutamic acid based on halophilic bacteria 清华大学 2022-10-21 CN disclosed
CN-113201514-B Polypeptides having aspartokinase activity and their use for producing amino acids 中国科学院天津工业生物技术研究所 2022-09-06 CN disclosed
WO-2007011939-A2 USE OF DIMETHYL DISULFIDE FOR METHIONINE PRODUCTION IN MICROORGANISMS BASF AG (DE) 2007-01-25 WO disclosed
CN-1333361-A Novel polypeptide--human L-3-phosphoserine phosphatase 10.01 and polynucleotide for encoding said polypeptide BODE GENE DEV CO LTD SHANGHAI (CN) 2002-01-30 CN disclosed
CN-1068351-C Prepn. method and application of amino acid condensation polymers and their hydrolytic products RHONE POULENC CHIMIE (FR) 2001-07-11 CN disclosed
US-5824765-A Preparation of polycondensates of amino acids and the biodegradable polypeptide hydrolysates thereof RHONE-POULENC CHIMIE (FR) 1998-10-20 US disclosed
US-5688903-A Process for the preparation of polycondensates of amino acids and the biodegradable polypeptide hydrolysates thereof, and their use in detergent compositions RHONE-POULENC CHIMIE (FR) 1997-11-18 US disclosed
CN-1128771-A Prepn. method and application of amino acid condensation polymers and their hydrolytic products RHONE POULENC CHIMIE (FR) 1996-08-14 CN disclosed
US-5009994-A Uniform distribution EM DIAGNOSTIC SYSTEMS, INC. (US) 1991-04-23 US disclosed
US-4820627-A SPRAYING AQUEOUS SOLUTIONS OF LABILE BIOCHEMICALS ONTO BULKING AGENTS EM DIAGNOSTIC SYSTEMS, INC. (US) 1989-04-11 US disclosed
US-4390625-A ERGOCORNINE AND ERGOCRYPTINE RICHTER GEDEON VEGYESZETI GYAR RT (HU) 1983-06-28 US disclosed