SCHEMBL1446973

SCHEMBL1446973

O=C([O-])Cc1ccc(O)cc1.[Na+]

nearest known ligand 0.64

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.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 4/20 0.62
CA1 known ✓ P00915 1/20 0.52
ESR2 known ✓ Q92731 3/20 0.48
CAMK2A Q9UQM7 1/20 0.62
FNTA P49354 1/20 0.61
FNTB P49356 1/20 0.61
CTBP2 P56545 1/20 0.50
ESR1 P03372 3/20 0.48
NPC1 O15118 2/20 0.48
RAB9A P51151 2/20 0.48
SHBG P04278 1/20 0.48
LMNA P02545 1/20 0.44
ABAT P80404 1/20 0.44
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
SENP1 Q9P0U3 1/20 0.43
CES2 O00748 1/20 0.42
CES1 P23141 1/20 0.42
SLC7A5 Q01650 1/20 0.42

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
SCHEMBL10958914 0.95 CA2 (0.62) CA2CAMK2AFNTAFNTBCA1
Potassium Ion SCHEMBL10912220 0.95 CA2 (0.62) CA2CAMK2AFNTAFNTBCA1
Lithium Ion SCHEMBL3811946 0.95 CA2 (0.62) CA2CAMK2AFNTAFNTBCA1
Hydroxyphenyl Propionic Acid SCHEMBL10954581 0.79 ESR1 (0.54) CA2CAMK2AFNTAFNTBCA1
Bicarbonate SCHEMBL27669090 0.79 CA2 (0.83) CA2CAMK2AFNTAFNTBCTBP2
SCHEMBL7150590 0.79 CA2 (0.68) CA2CAMK2AFNTAFNTBCA1
SCHEMBL9644305 0.78 TDP1 (0.46) CA2CA1CES2CES1
SCHEMBL17003351 0.78 CA2 (0.54) CA2CAMK2AFNTAFNTBCA1
4-Hydroxyphenylpyruvic Acid SCHEMBL24157 0.78 FNTA (0.72) CA2CAMK2AFNTAFNTBCTBP2
SCHEMBL3787818 0.78 CA1 (0.54) CA2CA1NPC1RAB9ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115010679-B Synthesis method of water-soluble benzoxazine 濮阳市恩赢高分子材料有限公司 2024-01-23 CN claimed
CN-114085343-A Modified sulfonated phenolic resin filtrate reducer for drilling fluid and preparation method thereof 中石化石油工程技术服务有限公司 2022-02-25 CN claimed
CN-106554266-B Preparation method of methoxyphenylacetic acid, intermediate thereof and salt thereof 联化科技(盐城)有限公司 2020-02-11 CN claimed
US-5500668-A INK JET PRINTING XEROX CORPORATION (US) 1996-03-19 US claimed
CN-116622354-B Biological chelating agent, scale remover and method for removing biological sulfide scale of oil and gas reservoir 中国石油天然气集团有限公司 2024-08-27 CN disclosed
CN-115010679-B Synthesis method of water-soluble benzoxazine 濮阳市恩赢高分子材料有限公司 2024-01-23 CN disclosed
CN-116622354-A Biological chelating agent, scale remover and method for removing biological sulfide scale of oil and gas reservoir 中国石油天然气集团有限公司 2023-08-22 CN disclosed
CN-114796246-B Medicine for treating heart failure and application thereof 佳木斯大学 2023-08-04 CN disclosed
CN-110652585-B Polysaccharide-protein conjugate immune preparation and application thereof 武汉博沃生物科技有限公司 2023-05-26 CN disclosed
CN-115010679-A Synthetic method of water-soluble benzoxazine 濮阳市恩赢高分子材料有限公司 2022-09-06 CN disclosed
CN-114796246-A Medicine for treating heart failure and application thereof 佳木斯大学 2022-07-29 CN disclosed
CN-114085343-A Modified sulfonated phenolic resin filtrate reducer for drilling fluid and preparation method thereof 中石化石油工程技术服务有限公司 2022-02-25 CN disclosed
EP-1355673-A2 MULTIVALENT MENINGOCOCCAL POLYSACCHARIDE-PROTEIN CONJUGATE VACCINE Aventis Pasteur (US) 2003-10-29 EP disclosed
US-20030068336-A1 Purified capsular polysaccharides from Neisseria meningitidis serogroups are activated and attached to a carriers protein SANOFI PASTEUR INC. 2003-04-10 US disclosed
WO-2002058737-A2 MULTIVALENT MENINGOCOCCAL POLYSACCHARIDE-PROTEIN CONJUGATE VACCINE AVENTIS PASTEUR (US) 2002-08-01 WO disclosed
US-6350795-B1 ACOUSTIC PHASE-CHANGE CONDUCTIVE INK CONTAINING LOW MOLECULAR WEIGHT OXYALKYLENE SEGMENTS COMPLEXED WITH UREA DERIVATIVES XEROX CORPORATION 2002-02-26 US disclosed
US-6096125-A Ink compositions XEROX CORPORATION (US) 2000-08-01 US disclosed
US-5500668-A INK JET PRINTING XEROX CORPORATION (US) 1996-03-19 US disclosed
US-4537724-A Alkanoyloxybenzenesulfonate salt production ETHYL CORPORATION (US) 1985-08-27 US disclosed
EP-0125641-A2 Alkanoyloxybenzenesulfonate salt production ETHYL CORPORATION (US) 1984-11-21 EP disclosed