SCHEMBL4277329

SCHEMBL4277329

CC(C)(C)N(C(=O)c1cccc([O-])c1)C(C)(C)C.[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 17)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.43
CYP2C9 P11712 1/20 0.43
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
TDP1 Q9NUW8 2/20 0.37
HPGD P15428 1/20 0.37
ABCB1 P08183 2/20 0.36
ACHE P22303 3/20 0.36
POLB P06746 1/20 0.36
ERN1 O75460 1/20 0.33
LMNA P02545 1/20 0.33
HSD17B1 P14061 1/20 0.33
HSD17B2 P37059 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
ALDH1A1 P00352 1/20 0.33
TSHR P16473 1/20 0.33
HSD17B10 Q99714 1/20 0.33

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
SCHEMBL7898354 0.79 CYP3A4 (0.49) CYP3A4CYP2C9MEN1KMT2ATDP1
SCHEMBL4284750 0.79 CA12 (0.52) CYP3A4CYP2C9HSD17B1HSD17B2ALDH1A1
SCHEMBL15339830 0.79 HPGD (0.59) CYP3A4CYP2C9MEN1KMT2ATDP1
SCHEMBL12084828 0.77 CES2 (0.55) CYP3A4CYP2C9MEN1KMT2AALDH1A1
SCHEMBL26398184 0.76 CYP3A4 (0.40) CYP3A4CYP2C9MEN1KMT2ATDP1
SCHEMBL11122024 0.75 POLB (0.56) CYP3A4CYP2C9TDP1HPGDPOLB
SCHEMBL12084023 0.75 CES2 (0.61) MEN1KMT2AHPGDABCB1POLB
SCHEMBL12084895 0.73 GSK3B (0.51) CYP3A4CYP2C9MEN1KMT2APOLB
SCHEMBL13640725 0.73 CYP3A4 (0.41) CYP3A4CYP2C9MEN1KMT2ATDP1
SCHEMBL22221326 0.71 ACHE (0.46) CYP3A4CYP2C9MEN1KMT2AABCB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7608731-B2 Phenylacetic acid compounds ROCHE PALO ALTO LLC (US) 2009-10-27 US disclosed
US-20080108810-A1 Phenylacetic acid compounds ROCHE PALO ALTO LLC 2008-05-08 US disclosed
US-7291729-B2 Process for preparing 3-aryloxy-phenylacetic acid compounds ROCHE PALO ALTO LLC (US) 2007-11-06 US disclosed
EP-1737827-A1 PROCESS FOR PREPARING PYRIDAZINONE COMPOUNDS F.HOFFMANN-LA ROCHE AG (CH) 2007-01-03 EP disclosed
WO-2005100323-A1 PROCESS FOR PREPARING PYRIDAZINONE COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2005-10-27 WO disclosed
US-20050234236-A1 Process for preparing pyridazinone compounds ROCHE PALO ALTO LLC 2005-10-20 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080108810-A1 Phenylacetic acid compounds CYP2A6, CYP2B6, DDC CYP3A4 100/4885CYP2C9 288/4885MEN1 3993/4885
US-20050234236-A1 Process for preparing pyridazinone compounds CYP2A6, CYP2B6, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 CYP3A4 73/4885CYP2C9 226/4885MEN1 3802/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.