SCHEMBL379185

SCHEMBL379185

[H+].[H+].[Na+].[O-]B([O-])[O-]

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
SCHEMBL379129 1.00
SCHEMBL6678589 1.00
SCHEMBL11652173 1.00
SCHEMBL2941169 1.00
Potassium Ion SCHEMBL21714273 0.93
Lithium Ion SCHEMBL21714352 0.93
SCHEMBL8925484 0.91
SCHEMBL1568303 0.91
SCHEMBL2817974 0.91
SCHEMBL168198 0.91

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-115260341-A High-quality agarose and preparation method thereof 国药集团化学试剂有限公司 2022-11-01 CN claimed
CN-110205463-B Treatment process of pin shaft 乐清海创智能科技有限公司 2021-08-06 CN claimed
CN-110195147-B Preparation method of pin shaft for large medical equipment 丁亮 2021-07-09 CN claimed
US-9410039-B2 Process for preparing surface-reacted calcium carbonate and its use OMYA INTERNATIONAL AG (CH) 2016-08-09 US claimed
US-9403988-B2 Process for preparing surface-reacted calcium carbonate and its use OMYA INTERNATIONAL AG (CH) 2016-08-02 US claimed
US-20140319412-A1 PROCESS FOR PREPARING SURFACE-REACTED CALCIUM CARBONATE AND ITS USE OMYA INTERNATIONAL AG (CH) 2014-10-30 US claimed
US-8809582-B2 Process for preparing surface-reacted calcium carbonate and its use OMYA INTERNATIONAL AG (CH) 2014-08-19 US claimed
US-8785687-B2 For preparing surface-reacted calcium carbonate and its use OMYA INTERNATIONAL AG (CH) 2014-07-22 US claimed
US-20130324762-A1 PROCESS FOR PREPARING SURFACE-REACTED CALCIUM CARBONATE AND ITS USE OMYA INTERNATIONAL AG (CH) 2013-12-05 US claimed
US-20130323489-A1 PROCESS FOR PREPARING SURFACE-REACTED CALCIUM CARBONATE AND ITS USE OMYA INTERNATIONAL AG (CH) 2013-12-05 US claimed
US-20120142965-A1 FOR PREPARING SURFACE-REACTED CALCIUM CARBONATE AND ITS USE OMYA INTERNATIONAL AG (CH) 2012-06-07 US claimed
EP-2264109-B1 Process for preparing surface-reacted calcium carbonate and its use OMYA DEVELOPMENT AG (CH) 2012-01-25 EP claimed
WO-2010146531-A1 PROCESS FOR PREPARING SURFACE-REACTED CALCIUM CARBONATE AND ITS USE OMYA DEVELOPMENT AG (CH) 2010-12-23 WO claimed
EP-2264109-A1 Process for preparing surface-reacted calcium carbonate and its use Omya Development AG (CH) 2010-12-22 EP claimed
EP-0979814-B1 Improved synthesis of haloformimine compounds ROHM & HAAS (US) 2003-10-22 EP claimed
US-6207863-B1 MAINTAINING A PH BETWEEN 2 AND 5 DURING THE HALOGENATION OF FORMIMINES GREATLY INCREASES THE YIELDS OF HALOFORMIMINES AND GREATLY DECREASES THE RATE OF BY-PRODUCT FORMATION. ROHM AND HAAS COMPANY 2001-03-27 US claimed
EP-0979814-A1 Improved synthesis of haloformimine compounds ROHM AND HAAS COMPANY (US) 2000-02-16 EP claimed
US-12623188-B2 Forward osmosis driven by electrolysis PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2026-05-12 US disclosed
EP-0979814-A1 Improved synthesis of haloformimine compounds ROHM AND HAAS COMPANY (US) 2000-02-16 EP disclosed
US-4257944-A CYANATION WITH A NONMETALLIC NITRILE IN THE PRESENCE OF A COPPER CATALYST IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1981-03-24 US disclosed