SCHEMBL3202942

SCHEMBL3202942

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

nearest known ligand 0.00

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL1463995 0.94 MGAM (0.52)
Potassium Ion SCHEMBL344530 0.94
SCHEMBL3181127 0.94
Lithium Ion SCHEMBL3197975 0.94
SCHEMBL3180441 0.94
SCHEMBL25276832 0.94 MGAM (0.52)
Lithium Ion SCHEMBL15950214 0.94 MGAM (0.52)
Tetramethylammonium Ion SCHEMBL4772224 0.89 MGAM (0.48)
Tetrylammonium SCHEMBL4773294 0.83 MGAM (0.42)
Acetoacetic Acid SCHEMBL29060526 0.79 MGAM (0.71)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117865974-A Synthesis method of Rhynchines A-E compound 陕西师范大学 2024-04-12 CN claimed
EP-1878493-B1 Method of making a polyisocyanurate/polyurethane foam using carbocation compounds as trimerization catalysts AIR PROD & CHEM (US) 2013-08-21 EP claimed
US-20080015274-A1 Stabilized carbanions as trimerization catalysts EVONIK OPERATIONS GMBH (DE) 2008-01-17 US claimed
EP-1878493-A1 Stabilized carbanions as trimerization catalysts Air Products and Chemicals, Inc. (US) 2008-01-16 EP claimed
CN-117865974-A Synthesis method of Rhynchines A-E compound 陕西师范大学 2024-04-12 CN disclosed
US-11680923-B2 Technologies using surface-modified pseudo-graphite ABB SCHWEIZ AG (CH) 2023-06-20 US disclosed
US-20230107216-A1 PANTETHEINE DERIVATIVES AND USES THEREOF VECTIVBIO COMET AG, F/K/A COMET THERAPEUTICS, INC. (CH) 2023-04-06 US disclosed
EP-3887353-A1 PANTETHEINE DERIVATIVES AND USES THEREOF Comet Therapeutics, Inc. (US) 2021-10-06 EP disclosed
US-20200284751-A1 Technologies Using Surface-Modified Pseudo-Graphite ABB SCHWEIZ AG (CH) 2020-09-10 US disclosed
WO-2020113209-A1 PANTETHEINE DERIVATIVES AND USES THEREOF COMET THERAPEUTICS, INC. (US) 2020-06-04 WO disclosed
EP-1878493-B1 Method of making a polyisocyanurate/polyurethane foam using carbocation compounds as trimerization catalysts AIR PROD & CHEM (US) 2013-08-21 EP disclosed
US-8445555-B2 Stabilized carbanions as trimerization catalysts AIR PRODUCTS AND CHEMICALS, INC. (US) 2013-05-21 US disclosed
US-4306079-A Novel ester derivatives of polycarboxylic acids and process for making same LEVER BROTHERS COMPANY (US) 1981-12-15 US disclosed
US-4299773-A Ester derivatives of polycarboxylic acids and process for making same LEVER BROTHERS COMPANY (US) 1981-11-10 US disclosed
US-4275007-A β-Lactone esters LEVER BROTHERS COMPANY (US) 1981-06-23 US disclosed
US-4273935-A Salts of propene 1,1,2,3-tetracarboxylic acid LEVER BROTHERS COMPANY (US) 1981-06-16 US disclosed
US-4218381-A Novel ester derivatives of polycarboxylic acids and process for making same LEVER BROTHERS COMPANY (US) 1980-08-19 US disclosed
US-4209636-A Preparation of ester derivatives of polycarboxylic acids LEVER BROTHERS COMPANY (US) 1980-06-24 US disclosed
US-4159388-A Ester derivatives of 1-halo-1,1,2,3-propane tetracarboxylic acid LEVER BROTHERS COMPANY (US) 1979-06-26 US disclosed
US-4123458-A HALOGENATION, DEHYDROGENATION, DECARBOXYLATION LEVER BROTHERS COMPANY (US) 1978-10-31 US disclosed