SCHEMBL3904265

SCHEMBL3904265

O=S(=O)([O-])CCN1CCN(CCO)CC1.O=S(=O)([O-])CCN1CCN(CCO)CC1.[Na+].[Na+]

nearest known ligand 0.42

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 20)

geneUniProtsupporting neighboursconfidence
CA12 known ✓ O43570 1/20 0.38
CA1 known ✓ P00915 1/20 0.38
CA2 known ✓ P00918 1/20 0.38
ALDH1A1 P00352 3/20 0.42
KDM4E B2RXH2 2/20 0.42
CA9 Q16790 1/20 0.38
CHRM2 P08172 1/20 0.37
CHRM1 P11229 1/20 0.37
KMT2A Q03164 4/20 0.36
LMNA P02545 1/20 0.36
HTT P42858 1/20 0.36
MEN1 O00255 2/20 0.36
GAA P10253 1/20 0.35
CYP3A4 P08684 2/20 0.35
CYP2C19 P33261 2/20 0.35
CYP2C9 P11712 1/20 0.35
HSD11B1 P28845 1/20 0.35
MAPT P10636 3/20 0.34
ALOX15 P16050 1/20 0.34
NPSR1 Q6W5P4 1/20 0.33

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
SCHEMBL229142 1.00 ALDH1A1 (0.42) ALDH1A1KDM4ECA12CA1CA2
Hydrochloric Acid SCHEMBL934319 0.98 ALDH1A1 (0.41) ALDH1A1KDM4ECA12CA1CA2
Water SCHEMBL1121994 0.98 ALDH1A1 (0.41) ALDH1A1KDM4ECA12CA1CA2
SCHEMBL3717130 0.96 ALDH1A1 (0.42) ALDH1A1KDM4ECA12CA1CA2
SCHEMBL29552462 0.96 ALDH1A1 (0.42) ALDH1A1KDM4ECA12CA1CA2
SCHEMBL3365753 0.96 ALDH1A1 (0.42) ALDH1A1KDM4ECA12CA1CA2
Potassium Ion SCHEMBL366682 0.96 ALDH1A1 (0.42) ALDH1A1KDM4ECA12CA1CA2
SCHEMBL14894927 0.96 ALDH1A1 (0.42) ALDH1A1KDM4ECA12CA1CA2
Hydrochloric Acid SCHEMBL23532725 0.94 ALDH1A1 (0.41) ALDH1A1KDM4ECA12CA1CA2
Water SCHEMBL4269781 0.94 ALDH1A1 (0.41) ALDH1A1KDM4ECA12CA1CA2

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
CN-118584689-A Photodynamic bacteriostatic contact lens and product thereof 王德华 2024-09-03 CN claimed
CN-119386200-A Pesticide scavenger and preparation method and application thereof 苏州大学 2025-02-07 CN disclosed
CN-118584689-A Photodynamic bacteriostatic contact lens and product thereof 王德华 2024-09-03 CN disclosed
CN-110251456-B Preparation method and application of nanogel 苏州大学 2023-01-06 CN disclosed
US-7556933-B2 Reagent system and process for adenosine triphosphate monitoring LUMINULTRA TECHNOLOGIES LTD. (CA) 2009-07-07 US disclosed
US-20060073537-A1 Reagent system and process for adenosine triphosphate monitoring LUMINULTRA TECHNOLOGIES LTD. (CA) 2006-04-06 US disclosed