SCHEMBL8993575

SCHEMBL8993575

CO[PH](=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
SCHEMBL7120709 1.00
Methylamine SCHEMBL29287030 0.93
Potassium Ion SCHEMBL1674510 0.92
Zinc Ion SCHEMBL28390650 0.92
SCHEMBL2406804 0.92
Potassium Ion SCHEMBL7126706 0.92
SCHEMBL2174035 0.92
SCHEMBL29130614 0.92
SCHEMBL3310167 0.92
SCHEMBL23704367 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118183884-A Reutilization method of water-based fracturing flowback fluid and application thereof 北京爱普聚合科技有限公司 2024-06-14 CN claimed
CN-114507041-A Low-thixotropic ultrahigh-performance concrete and preparation method thereof 江苏苏博特新材料股份有限公司 2022-05-17 CN claimed
US-4414126-A ALKALI METAL MERCAPTOBENZOTHIAZOLE AND A PHOSPHONATE BASF WYANDOTTE CORPORATION (US) 1983-11-08 US claimed
CN-118183884-A Reutilization method of water-based fracturing flowback fluid and application thereof 北京爱普聚合科技有限公司 2024-06-14 CN disclosed
CN-112934473-B Application of copper-nickel sulfide ore flotation inhibitor in copper-nickel sulfide ore flotation 武汉理工大学 2023-08-15 CN disclosed
CN-111732253-B Seawater desalination pretreatment method for improving recovery rate 天津大学 2022-08-30 CN disclosed
CN-114507041-A Low-thixotropic ultrahigh-performance concrete and preparation method thereof 江苏苏博特新材料股份有限公司 2022-05-17 CN disclosed
CN-111732253-A Seawater desalination pretreatment method for improving recovery rate 天津大学 2020-10-02 CN disclosed
CN-101909579-B Cement for dental applications KURARAY MEDICAL INC 2013-11-20 CN disclosed
CN-103118626-A Dental mill blank KURARAY MEDICAL INC 2013-05-22 CN disclosed
CN-101909579-A Cement for dental applications KURARAY MEDICAL INC 2010-12-08 CN disclosed
US-5565616-A MIXING COMPOUND CONTAINING ALKYL BOUND TO HETEROATOM WITH ADDITIVE WHICH REACTS TO FORM SALT INSOLUBLE IN SUPERCRITICAL WATER, REACTING AT OXYGEN CONCENTRATION FAVORING ALKANE PRODUCTION, RECOVERING ALKANE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1996-10-15 US disclosed
US-4108746-A IRRADIATING TO INDUCE OXIDATION THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY (US) 1978-08-22 US disclosed