SCHEMBL7009018

SCHEMBL7009018

C/C(O)=C(\C#N)C(=O)[O-].[Na+]

nearest known ligand 0.41

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
CA4 known ✓ P22748 3/20 0.41
CA1 known ✓ P00915 2/20 0.38
THRB known ✓ P10828 1/20 0.34
DHODH Q02127 5/20 0.37
ALDH1A1 P00352 3/20 0.34
MEN1 O00255 2/20 0.34
KMT2A Q03164 2/20 0.34
CYP1A2 P05177 1/20 0.34
CYP3A4 P08684 1/20 0.34
GAA P10253 1/20 0.34
CYP2C9 P11712 1/20 0.34
PKM P14618 1/20 0.34
ALOX15 P16050 1/20 0.34
TSHR P16473 1/20 0.34
LMNA P02545 1/20 0.34
BLM P54132 1/20 0.34
BTK Q06187 1/20 0.34
NPSR1 Q6W5P4 1/20 0.34
PLK3 Q9H4B4 1/20 0.34
FAHD1 Q6P587 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
SCHEMBL7009022 1.00 CA4 (0.41) CA4CA1DHODHALDH1A1MEN1
SCHEMBL4507427 0.76
SCHEMBL4507423 0.76
SCHEMBL4507425 0.76
SCHEMBL12700930 0.76
Butane SCHEMBL16534920 0.73 CA1 (0.37) CA1CYP3A4TSHRNPSR1
SCHEMBL7180210 0.72
SCHEMBL30298582 0.72 CA4 (0.43) CA4CA1TSHR
SCHEMBL7180208 0.72
Acetic Acid SCHEMBL9078867 0.69 CA1 (0.53) CA4CA1MEN1KMT2ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1054859-A4 PROCESSES AND INTERMEDIATES USEFUL TO MAKE ANTIFOLATES LILLY CO ELI (US) 2003-03-05 EP disclosed
US-6426417-B1 CYCLIZATION OF A CYANO-ESTER DERIVATIVE WITH 2,6-DIAMINO-6-HYDROXYPYRIMIDINE IN THE PRESENCE OF ACETIC ACID AND ACETONITRILE ELI LILLY AND COMPANY 2002-07-30 US disclosed
EP-1054859-A1 PROCESSES AND INTERMEDIATES USEFUL TO MAKE ANTIFOLATES ELI LILLY AND COMPANY (US) 2000-11-29 EP disclosed
WO-1999041230-A1 PROCESSES AND INTERMEDIATES USEFUL TO MAKE ANTIFOLATES ELI LILLY AND COMPANY (US) 1999-08-19 WO disclosed