SCHEMBL6461630

SCHEMBL6461630

Cc1ccc(S(=O)(=O)[N-]Cl)cc1.O=C1CC(O)CN1.[Na+]

nearest known ligand 0.56

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 18)

geneUniProtsupporting neighboursconfidence
THRB known ✓ P10828 1/20 0.34
CA1 known ✓ P00915 1/20 0.33
CA2 known ✓ P00918 1/20 0.33
NOD2 known ✓ Q9HC29 2/20 0.32
GAA P10253 2/20 0.34
TSHR P16473 1/20 0.34
ALDH1A1 P00352 4/20 0.34
MAPT P10636 1/20 0.33
RECQL P46063 1/20 0.33
PKM P14618 1/20 0.33
CRBN Q96SW2 1/20 0.33
LMNA P02545 2/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
POLB P06746 1/20 0.32
HTT P42858 1/20 0.32
FPR1 P21462 1/20 0.32
FPR2 P25090 1/20 0.32
KMT2A Q03164 1/20 0.32

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
SCHEMBL8521486 0.79 MAPT (0.42) GAAALDH1A1MAPTRECQLPKM
Ammonia Solution, Strong SCHEMBL3915653 0.78 GAA (0.50) GAAALDH1A1MAPTPKMCA1
Ammonia Solution, Strong SCHEMBL11295239 0.78 GAA (0.50) GAAALDH1A1MAPTPKMCA1
Phosphine SCHEMBL7592008 0.78 GAA (0.50) GAAALDH1A1MAPTPKMCA1
SCHEMBL9283882 0.77 GAA (0.35) GAATSHRALDH1A1CRBNLMNA
SCHEMBL7046780 0.77 HTR6 (0.38) GAATSHRALDH1A1POLBKMT2A
SCHEMBL4726308 0.76 RAB9A (0.37) GAATSHRALDH1A1MAPTCRBN
Methyl Alcohol SCHEMBL7073942 0.76 GAA (0.48) GAAALDH1A1RECQLCA1CA2
Chloramine-T Anhydrous SCHEMBL19335 0.76 GAA (0.52) GAAALDH1A1MAPTPKMCA1
SCHEMBL31448661 0.76 GAA (0.52) GAAALDH1A1MAPTPKMCA1

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
EP-1325146-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE 4-HYDROXY-2-PYRROLIDINONE AND N-SUBSTITUTED 4-HYDROXY-2-PYRROLIDINONES BY ENZYMATIC HYDROXYLATION EIDGENOESSICHE TECH HOCHSCHULE (CH) 2005-12-14 EP claimed
EP-0947505-B1 Process for preparing optically active 4-hydroxy-2-pyrrolidone TAKASAGO PERFUMERY CO LTD (JP) 2002-07-17 EP claimed