Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5683126

C=CC(c1ccccc1)c1ccccc1C(=O)NC(C)N(C)C.Cl

nearest known ligand 0.45

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Hydrochloric Acid. 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
KCNB1 known ✓ Q14721 1/20 0.37
KCNB2 known ✓ Q92953 1/20 0.37
ALDH1A1 P00352 6/20 0.41
KDM4E B2RXH2 4/20 0.41
HPGD P15428 4/20 0.41
HSD17B10 Q99714 4/20 0.41
LMNA P02545 3/20 0.41
L3MBTL1 Q9Y468 2/20 0.37
MEN1 O00255 1/20 0.37
MAPT P10636 1/20 0.37
CYP2C9 P11712 1/20 0.37
KMT2A Q03164 1/20 0.37
TSHR P16473 1/20 0.36
MTOR P42345 1/20 0.35
NPSR1 Q6W5P4 1/20 0.34
POLB P06746 1/20 0.34
MAPK8 P45983 1/20 0.34

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
SCHEMBL29129651 0.77 CTSD (0.41) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL6278245 0.75 ALDH1A1 (0.49) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL7216545 0.72 MEN1 (0.41) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL9542306 0.72 KDM4E (0.41) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL5682092 0.72 MAPT (0.39) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL27432511 0.71 AKR1C3 (0.46) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL19437356 0.70 CXCR2 (0.44) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL3792769 0.70 AKR1C3 (0.44) ALDH1A1KDM4EHSD17B10LMNAMAPT
SCHEMBL20548792 0.68 MEN1 (0.44) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL860493 0.68 CYP2C19 (0.37) ALDH1A1KDM4EHPGDHSD17B10LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1131330-B1 CHEMILUMINESCENT SUBSTRATES FOR NEURAMINIDASE, ASSAYS FOR DETECTION OF NEURAMINIDASE AND KITS THEREFOR APPLERA CORP (US) 2006-03-08 EP disclosed
US-6555698-B1 A 3-(enzymatically cleavable 2-n-acetylneuraminic acid)spiro 1,2-dioxacyclobutane compound, e.g. spiro(adamantane-3,3'-1,2 -dioxabutane; diagnosis for the influenza virus, respiratory system infections; sensitivity; TROPIX, INC. 2003-04-29 US disclosed
EP-1131330-A4 CHEMILUMINESCENT SUBSTRATES FOR NEURAMINIDASE, ASSAYS FOR DETECTION OF NEURAMINIDASE AND KITS THEREFOR TROPIX INC (US) 2002-06-12 EP disclosed
EP-1131330-A1 CHEMILUMINESCENT SUBSTRATES FOR NEURAMINIDASE, ASSAYS FOR DETECTION OF NEURAMINIDASE AND KITS THEREFOR TROPIX, INC. (US) 2001-09-12 EP disclosed
WO-2000029419-A1 CHEMILUMINESCENT SUBSTRATES FOR NEURAMINIDASE, ASSAYS FOR DETECTION OF NEURAMINIDASE AND KITS THEREFOR TROPIX, INC. (US) 2000-05-25 WO disclosed
EP-0619018-B1 IMPROVED MEMBRANE FOR CHEMILUMINESCENT BLOTTING APPLICATIONS TROPIX INC (US) 1998-11-25 EP disclosed
EP-0619018-A4 IMPROVED MEMBRANE FOR CHEMILUMINESCENT BLOTTING APPLICATIONS. TROPIX INC (US) 1997-01-15 EP disclosed
US-5593828-A Membrane for chemiluminescent blotting applications TROPIX, INC. (US) 1997-01-14 US disclosed
EP-0619018-A1 IMPROVED MEMBRANE FOR CHEMILUMINESCENT BLOTTING APPLICATIONS TROPIX, INC. (US) 1994-10-12 EP disclosed
US-5336596-A Polymer coated support; 1,2-dioxetanes as chemiluminescence source TROPIX, INC. (US) 1994-08-09 US disclosed
WO-1993013405-A1 IMPROVED MEMBRANE FOR CHEMILUMINESCENT BLOTTING APPLICATIONS TROPIX, INC. (US) 1993-07-08 WO disclosed