SCHEMBL1965312

SCHEMBL1965312

[Na+].[NaH].[O-]Cl

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
SCHEMBL5544620 0.89
Sodium Hypochlorite SCHEMBL5239 0.89
SCHEMBL9842290 0.89
SCHEMBL5465998 0.80
SCHEMBL3195381 0.80
SCHEMBL6828918 0.80
Potassium Ion SCHEMBL14739178 0.80
SCHEMBL6828919 0.80
Water SCHEMBL9463314 0.80
Bromide SCHEMBL1831908 0.80

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109045963-A A kind of method that oxidation-absorption removes gaseous state selenium dioxide in coal-fired flue-gas 华北电力大学 2018-12-21 CN claimed
JP-62290136-A None JP disclosed
US-11603596-B2 Electrolytic cell for hypochlorite generation Electrichlor, LLC (US) 2023-03-14 US disclosed
CN-115109022-A Preparation method of 5, 7-difluorochroman-4-one 常州工程职业技术学院 2022-09-27 CN disclosed
EP-3956330-A1 SUBSTITUTED 2-AMINO-PYRAZOLYL-[1,2,4]TRIAZOLO[1,5A] PYRIDINE DERIVATIVES AND USE THEREOF The Johns Hopkins University (US) 2022-02-23 EP disclosed
WO-2020215094-A1 SUBSTITUTED 2-AMINO-PYRAZOLYL-[1,2,4]TRIAZOLO[1,5A] PYRIDINE DERIVATIVES AND USE THEREOF THE JOHNS HOPKINS UNIVERSITY (US) 2020-10-22 WO disclosed
US-20200291534-A1 ELECTROLYTIC CELL FOR HYPOCHLORITE GENERATION ELECTRICHLOR TECHNOLOGIES LLC 2020-09-17 US disclosed
CN-108498539-A A kind of preparation method of water solubility chalybeate complex bulk pharmaceutical chemicals 东营天东制药有限公司 2018-09-07 CN disclosed
CN-104074085-B The multistage catalysis carboxylation of mercerized cellulose fiber 韦尔豪泽NR公司 2016-08-10 CN disclosed
EP-2334636-A2 HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS Pfizer Inc. (US) 2011-06-22 EP disclosed
WO-2010032147-A2 HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS PFIZER INC. (US) 2010-03-25 WO disclosed
EP-1833920-A2 IMPROVEMENTS IN OR RELATING TO BIODEGRADABLE COMPOSITES KORDE, Shree Prakash (GB) 2007-09-19 EP disclosed
WO-2006059112-A2 IMPROVEMENTS IN OR RELATING TO BIODEGRADABLE COMPOSITES KORDE, SHREE, PRAKASH (GB) 2006-06-08 WO disclosed
JP-S62290136-A MIRROR POLISHING LIQUID FOR GAAS WAFER NIPPON MINING CO LTD 1987-12-17 JP disclosed