SCHEMBL10583900

SCHEMBL10583900

O=[PH]([O-])O[PH](=O)[O-].O=[PH]([O-])O[PH](=O)[O-].[Na+].[Na+].[Na+].[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
SCHEMBL1168334 1.00 — —
Ethylene SCHEMBL30862405 0.92 — —
SCHEMBL18187089 0.91 — —
SCHEMBL18187078 0.91 — —
SCHEMBL8335757 0.91 — —
SCHEMBL18187385 0.91 — —
SCHEMBL18187185 0.91 — —
SCHEMBL18188042 0.91 — —
SCHEMBL7735578 0.91 — —
SCHEMBL3782878 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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024152094-A1 METHOD FOR REDUCING THE COLOURING OF SUGAR, PROCESS FOR PRODUCING SUGAR WITH LOW COLOUR, COMPOSITION AND USE OF A CHELATING AGENT ITALMATCH CHEMICALS SPA (IT) 2024-07-25 — — WO claimed
EP-4389885-B1 ALPHA-AMYLASE VARIANTS DANISCO US INC (US) 2025-09-03 — — EP disclosed
WO-2024152094-A1 METHOD FOR REDUCING THE COLOURING OF SUGAR, PROCESS FOR PRODUCING SUGAR WITH LOW COLOUR, COMPOSITION AND USE OF A CHELATING AGENT ITALMATCH CHEMICALS SPA (IT) 2024-07-25 — — WO disclosed
WO-2022231005-A1 OXIDATION HAIR DYE, FIRST AGENT FOR OXIDATION HAIR DYE, AND USAGE METHOD FOR OXIDATION HAIR DYE ホーユー株式会社 2022-11-03 — — WO disclosed
CN-101337919-A Method for synthesizing high-stability thiourea dioxide HENAN HONGYE CHEMICAL CO LTD (CN) 2009-01-07 — — CN disclosed
US-4828766-A FROM 1-/ACYL/-ETHANE-1,1-DIPHOSPHONIC ACID BENCKISER-KNAPSACK GMBH (DE) 1989-05-09 — — US disclosed
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