SCHEMBL4438868

SCHEMBL4438868

CC(O)Oc1ccccc1.O=C([O-])CNCO.[Na+]

nearest known ligand 0.43

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
MTNR1A P48039 1/20 0.43
MTNR1B P49286 1/20 0.43
POLB P06746 2/20 0.41
HPGD P15428 1/20 0.40
GAA P10253 2/20 0.40
CYP1A2 P05177 1/20 0.40
CYP2C9 P11712 1/20 0.40
PKM P14618 1/20 0.40
CYP2C19 P33261 1/20 0.40
TAS1R3 Q7RTX0 1/20 0.40
TAS1R1 Q7RTX1 1/20 0.40
TAS1R2 Q8TE23 1/20 0.40
ADRB3 P13945 5/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
RXFP1 Q9HBX9 1/20 0.39
TSHR P16473 2/20 0.38
TDP1 Q9NUW8 1/20 0.38

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
Propionic Acid SCHEMBL28882997 0.80 MTNR1A (0.45) MTNR1AMTNR1BPOLBHPGDGAA
Glycolic Acid SCHEMBL20271336 0.78 MTNR1A (0.46) MTNR1AMTNR1BPOLBHPGDGAA
Benzoic Acid SCHEMBL20515481 0.76 CA2 (0.59) MTNR1AMTNR1BPOLBHPGDGAA
Phenoxyethanol SCHEMBL4438865 0.76 RECQL (0.59) MTNR1AMTNR1BHPGDGAACYP1A2
Glycinebetaine SCHEMBL9710566 0.75 MTNR1A (0.39) MTNR1AMTNR1BPOLBHPGDGAA
Ethylene Glycol SCHEMBL9388302 0.75 LMNA (0.50) MTNR1AMTNR1BPOLBGAACYP1A2
Alcohol SCHEMBL4086513 0.75 LMNA (0.50) MTNR1AMTNR1BPOLBGAACYP1A2
Acetic Acid SCHEMBL27465373 0.75 MTNR1A (0.53) MTNR1AMTNR1BPOLBHPGDGAA
Zinc Ion SCHEMBL3838825 0.75 LMNA (0.48) MTNR1AMTNR1BPOLBHPGDGAA
Hydrochloric Acid SCHEMBL28169465 0.75 LMNA (0.48) MTNR1AMTNR1BPOLBHPGDGAA

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-2124871-A2 FORMULATION FOR INCREASING THE ACTIVITY OF A PLANT EXTRACT FOR COSMETIC USE AND COSMETIC PREPARATION WHICH COMPRISES THE SAME LABO Cosprophar AG (CH) 2009-12-02 EP disclosed
WO-2008104570-A2 FORMULATION FOR INCREASING THE ACTIVITY OF A PLANT EXTRACT FOR COSMETIC USE AND COSMETIC PREPARATION WHICH COMPRISES THE SAME LABO COSPROPHAR AG (CH) 2008-09-04 WO disclosed