SCHEMBL11426005

SCHEMBL11426005

O=C([O-])c1ccc(NCc2ccc3c(c2)OCO3)cc1.[Na+]

nearest known ligand 0.67

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 0.57
MEN1 O00255 6/20 0.67
KMT2A Q03164 6/20 0.67
MAPT P10636 5/20 0.67
ALDH1A1 P00352 5/20 0.67
LMNA P02545 4/20 0.67
ALOX15 P16050 3/20 0.67
USP2 O75604 2/20 0.67
HSD17B10 Q99714 1/20 0.67
ALOX12 P18054 3/20 0.57
GAA P10253 2/20 0.57
TDP1 Q9NUW8 2/20 0.57
KDM4E B2RXH2 2/20 0.57
INSR P06213 2/20 0.56
IGF1R P08069 2/20 0.56
SRC P12931 1/20 0.56
MAPK1 P28482 3/20 0.55
SMN1; SMN2 Q16637 3/20 0.55
L3MBTL1 Q9Y468 2/20 0.55
HTT P42858 2/20 0.55

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
SCHEMBL11230733 0.86 ALDH1A1 (0.70) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL11426003 0.85 ALDH1A1 (0.68) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL11236972 0.80 MAPT (1.00) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL10057818 0.80 INSR (0.77) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL2979012 0.77 MAPT (0.64) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL19476128 0.77 ALDH1A1 (0.83) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL11119339 0.77 MEN1 (0.65) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL9672474 0.77 MAPT (0.63) MEN1KMT2AMAPTALDH1A1LMNA
Hydrochloric Acid SCHEMBL2989075 0.76 MAPT (0.63) MEN1KMT2AMAPTALDH1A1LMNA
SCHEMBL29245024 0.75 ALDH1A1 (0.69) MEN1KMT2AMAPTALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4206223-A Method for treating hyperglycemia in mammals using 4-(((1,3-benzodioxol-5-yl)methyl)amino)benzoic acid or derivatives thereof THE DOW CHEMICAL COMPANY (US) 1980-06-03 US disclosed
US-4133890-A Hypolipidemic compositions and method employing derivatives of 4-(((1,3-benzodioxol-5-yl)methyl)amino)benzoic acid THE DOW CHEMICAL COMPANY (US) 1979-01-09 US disclosed