SCHEMBL29883166

SCHEMBL29883166

O=S(=O)([O-])c1ccc(N=Nc2ccc(N=Nc3c(O)c(S(=O)(=O)[O-])cc4cc(S(=O)(=O)[O-])ccc34)c(S(=O)(=O)[O-])c2)cc1.[Na+].[Na+].[Na+].[Na+]

nearest known ligand 0.60

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
THRB known ✓ P10828 2/20 0.60
CD40 P25942 1/20 0.51
CD40LG P29965 1/20 0.51
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
TDP1 Q9NUW8 1/20 0.50
ALDH1A1 P00352 2/20 0.49
HIF1A Q16665 2/20 0.49
ENPP2 Q13822 1/20 0.49
CYP1A2 P05177 2/20 0.47
PTPN7 P35236 1/20 0.47
PTPN11 Q06124 1/20 0.47
PTPN1 P18031 3/20 0.46
USP2 O75604 1/20 0.45
ATM Q13315 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
APEX1 P27695 2/20 0.45
SLC7A11 Q9UPY5 2/20 0.45
APP P05067 1/20 0.44
POLB P06746 1/20 0.43

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
SCHEMBL1598800 1.00 THRB (0.60) THRBCD40CD40LGMEN1KMT2A
SCHEMBL29373132 1.00 THRB (0.60) THRBCD40CD40LGMEN1KMT2A
SCHEMBL26385 1.00 THRB (0.60) THRBCD40CD40LGMEN1KMT2A
SCHEMBL9406984 0.92 THRB (0.53) THRBCD40CD40LGMEN1KMT2A
SCHEMBL30337585 0.86 THRB (0.62) THRBMEN1KMT2ATDP1ALDH1A1
SCHEMBL127635 0.86 THRB (0.62) THRBMEN1KMT2ATDP1ALDH1A1
SCHEMBL29527953 0.83 ALDH1A1 (0.57) THRBMEN1KMT2ATDP1ALDH1A1
Amaranth SCHEMBL185413 0.83 THRB (0.72) THRBMEN1KMT2ATDP1ALDH1A1
Amaranth SCHEMBL8618995 0.83 THRB (0.72) THRBMEN1KMT2ATDP1ALDH1A1
Amaranth SCHEMBL29352916 0.83 THRB (0.72) THRBMEN1KMT2ATDP1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113603177-B Reconfigurable and regenerative azo dye adsorption method and application thereof 北京航空航天大学 2022-09-27 CN disclosed