Acetonitrile

Acetonitrile

SCHEMBL5226956

CC#N.CC1CN(CC(=O)O)[C@H](c2ccccc2Cl)c2ccsc21.O.O=S(=O)(O)c1cccc2c(S(=O)(=O)O)cccc12

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Acetonitrile. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
HTR6 known ✓ P50406 1/20 0.30
KDM4E B2RXH2 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
RXFP1 Q9HBX9 1/20 0.32
CYP1A2 P05177 1/20 0.32
SLC6A9 P48067 6/20 0.32
FDFT1 P37268 1/20 0.30

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
SCHEMBL5228846 0.96 KDM4E (0.38) KDM4ENPSR1RXFP1CYP1A2SLC6A9
Bromide SCHEMBL5238372 0.85 KDM4E (0.45) KDM4ENPSR1RXFP1SLC6A9FDFT1
SCHEMBL15937933 0.85 KDM4E (0.46) KDM4ENPSR1RXFP1SLC6A9FDFT1
SCHEMBL3901210 0.85 KDM4E (0.46) KDM4ENPSR1RXFP1SLC6A9FDFT1
Bromide SCHEMBL5236979 0.84 KDM4E (0.46) KDM4ENPSR1RXFP1SLC6A9FDFT1
Water SCHEMBL5231972 0.80 HHAT (0.39) KDM4ENPSR1CYP1A2
SCHEMBL1499083 0.77 KDM4E (0.46) KDM4ENPSR1RXFP1SLC6A9FDFT1
Sulfuric Acid SCHEMBL6377500 0.68 TSHR (0.34) KDM4ENPSR1
SCHEMBL4018143 0.66 HHAT (0.48) KDM4ENPSR1
SCHEMBL5439863 0.66 HHAT (0.48) KDM4ENPSR1

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-1740594-A1 CLOPIDOGREL SALT AND POLYMORPHIC FORMS THEREOF Sanofi-Aventis (FR) 2007-01-10 EP claimed
WO-2005103059-A1 CLOPIDOGREL SALT AND POLYMORPHIC FORMS THEREOF SANOFI-AVENTIS (FR) 2005-11-03 WO claimed
EP-1740594-A1 CLOPIDOGREL SALT AND POLYMORPHIC FORMS THEREOF Sanofi-Aventis (FR) 2007-01-10 EP disclosed
WO-2005103059-A1 CLOPIDOGREL SALT AND POLYMORPHIC FORMS THEREOF SANOFI-AVENTIS (FR) 2005-11-03 WO disclosed