SCHEMBL22729973

SCHEMBL22729973

CC(Cc1ccc(OCC(=O)[O-])cc1)NCC(O)c1cccc(Cl)c1.[Na+]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 16)

geneUniProtsupporting neighboursconfidence
ADRB3 P13945 14/20 1.00
ADRB2 P07550 12/20 1.00
CYP2D6 P10635 2/20 1.00
CYP3A4 P08684 1/20 1.00
HIF1A Q16665 1/20 1.00
ADRB1 P08588 8/20 0.81
ADRA1D P25100 1/20 0.81
ADRA1A P35348 1/20 0.81
ADRA1B P35368 1/20 0.81
CYP1A2 P05177 1/20 0.81
CYP2C9 P11712 1/20 0.81
CYP2C19 P33261 1/20 0.81
GLA P06280 1/20 0.80
SLC2A1 P11166 4/20 0.71
ALOX15 P16050 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61

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
SCHEMBL6678497 1.00 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
Water SCHEMBL15421413 0.99 ADRB3 (0.98) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL304308 0.90 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL302998 0.90 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL304309 0.90 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL302999 0.90 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL3692642 0.90 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL5144151 0.89 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL9006835 0.89 ADRB3 (1.00) ADRB3ADRB2CYP2D6CYP3A4HIF1A
SCHEMBL4344462 0.89 ADRB3 (0.98) ADRB3ADRB2CYP2D6CYP3A4HIF1A

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
EP-2891490-B1 BETA-3 ADRENOCEPTOR AGONISTS FOR THE TREATMENT OF PULMONARY HYPERTENSION DUE TO LEFT HEART DISEASE FUNDACION CENTRO NAC DE INVESTIGACIONES CARDIOVASCULARES CARLOS III CNIC (ES) 2020-12-09 EP disclosed