Oxaloacetate

Oxaloacetate

SCHEMBL1469849

O=C([O-])CC(=O)C(=O)O.[Na+]

nearest known ligand 0.62

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Oxaloacetate. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ CA4 known ✓ P22748 3/20 0.62
▸ CA2 known ✓ P00918 1/20 0.35
▸ CA1 known ✓ P00915 1/20 0.33
▸ OR51E2 Q9H255 2/20 0.42
▸ CASP1 P29466 1/20 0.42
▸ FEN1 P39748 4/20 0.39
▸ ERCC5 P28715 3/20 0.39
▸ PTPN1 P18031 1/20 0.39
▸ MAPK1 P28482 1/20 0.38
▸ SLC13A3 Q8WWT9 1/20 0.38
▸ EGLN1 Q9GZT9 1/20 0.38
▸ FFAR3 O14843 1/20 0.36
▸ HDAC3 O15379 1/20 0.36
▸ HDAC1 Q13547 1/20 0.36
▸ HDAC2 Q92769 1/20 0.36
▸ HDAC8 Q9BY41 1/20 0.36
▸ HAO1 Q9UJM8 1/20 0.36
▸ FAHD1 Q6P587 1/20 0.35
▸ LMNA P02545 1/20 0.35

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
Oxaloacetate SCHEMBL31087912 1.00 CA4 (0.62) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL9994508 0.97 CA4 (0.60) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL28674017 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL29210051 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL29098309 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL7632482 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL6310312 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL9782823 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL11328363 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5
Oxaloacetate SCHEMBL31027133 0.93 CA4 (0.56) CA4OR51E2CASP1FEN1ERCC5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122080382-A Isosorbide type polycarbonate and preparation method thereof — 2026-05-26 — — CN claimed
WO-2025096390-A1 AUTO-EXPRESSION BROTH AND USES THEREOF UNIVERSITY OF MONTANA (US) 2025-05-08 — — WO claimed
CN-113881749-B Method for rapidly promoting astaxanthin accumulation in haematococcus pluvialis 中国科学院海洋研究所 2023-06-20 — — CN claimed
CN-113881749-A Method for rapidly promoting accumulation of astaxanthin in haematococcus pluvialis 中国科学院海洋研究所 2022-01-04 — — CN claimed
US-6129847-A SEPARATELY RECOVERING MAGNETIC POWDER AND SUBSTRATE MATERIAL BY TREATING WITH SOLUTION OF A POTASSIUM SALT OF A POLYUNSATURATED FATTY ACID, OR BIODEGRADEABLE CLEANING AGENT COMPRISING PHOSPHATES, SURFACTANTS, AND A COMPLEXING AGENT BASF MAGNETICS GMBH (DE) 2000-10-10 — — US claimed
EP-0749457-B1 PROCESS FOR RECOVERING RAW MATERIALS FROM MAGNETIC RECORDING CARRIERS EMTEC MAGNETICS GMBH (DE) 1998-07-29 — — EP claimed
CN-122080382-A Isosorbide type polycarbonate and preparation method thereof — 2026-05-26 — — CN disclosed
EP-3056199-B1 MODIFICATION OF THE PH AND OTHER PHYSICAL PROPERTIES OF OXALOACETIC ACID TO ALLOW FOR ENHANCED STABILITY CASH ALAN B (US) 2026-05-20 — — EP disclosed
US-20250262177-A1 METHOD TO ALLEVIATE THE SYMPTOMS OF PMS CASH ALAN B (US) 2025-08-21 — — US disclosed
US-12324794-B2 Method to alleviate the symptoms of PMS CASH ALAN B (US) 2025-06-10 — — US disclosed
WO-2025096390-A1 AUTO-EXPRESSION BROTH AND USES THEREOF UNIVERSITY OF MONTANA (US) 2025-05-08 — — WO disclosed
CN-114916559-B Low-temperature Leng Lian disinfectant and preparation method thereof 江苏豪凡医疗科技有限公司 2024-05-07 — — CN disclosed
US-20240115529-A1 METHOD TO ALLEVIATE THE SYMPTOMS OF PMS CASH ALAN B (US) 2024-04-11 — — US disclosed
US-6129847-A SEPARATELY RECOVERING MAGNETIC POWDER AND SUBSTRATE MATERIAL BY TREATING WITH SOLUTION OF A POTASSIUM SALT OF A POLYUNSATURATED FATTY ACID, OR BIODEGRADEABLE CLEANING AGENT COMPRISING PHOSPHATES, SURFACTANTS, AND A COMPLEXING AGENT BASF MAGNETICS GMBH (DE) 2000-10-10 — — US disclosed
US-5185434-A Inhibit protein synthsis; low-speed plasma elimination; anticarcinogenic agents SANOFI (FR) 1993-02-09 — — US disclosed
US-4900730-A USING CHELATING AGENT AND SOLVENT; HIGH OSMOTIC PRESSURE TOYO JOZO CO., LTD. (JP) 1990-02-13 — — US disclosed
US-4267268-A Spermatozoa extenders OLD STONE BANK, A RHODE ISLAND BANKING CORP. 1981-05-12 — — US disclosed
US-4126617-A PROPHYLAXIS THE UPJOHN COMPANY (US) 1978-11-21 — — US disclosed
US-3959289-A PROPHYLACTICS IN ALLERGIES THE UPJOHN COMPANY (US) 1976-05-25 — — US disclosed
US-3953598-A ASTHMA OR RHINITIS TREATMENT THE UPJOHN COMPANY (US) 1976-04-27 — — US disclosed
Send feedback