Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4440714

CCC[Si](OC)(OC)OC.Cl.NCC(N)Cc1ccccc1

nearest known ligand 0.53

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 16)

geneUniProtsupporting neighboursconfidence
SCN4A known ✓ P35499 2/20 0.42
SIGMAR1 known ✓ Q99720 4/20 0.41
TACR1 known ✓ P25103 1/20 0.40
SLC6A2 known ✓ P23975 2/20 0.40
MAOA known ✓ P21397 1/20 0.40
SLC6A4 known ✓ P31645 1/20 0.40
SLC6A3 known ✓ Q01959 1/20 0.40
EPHX1 P07099 1/20 0.46
ANPEP P15144 1/20 0.41
TAAR1 Q96RJ0 2/20 0.40
CYP2A6 P11509 1/20 0.40
ADORA2A P29274 1/20 0.40
ADORA1 P30542 1/20 0.40
MMP2 P08253 2/20 0.39
CSNK1E P49674 1/20 0.38
CYP2D6 P10635 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
SCHEMBL1138049 0.98 EPHX1 (0.47) EPHX1SCN4AANPEPSIGMAR1TACR1
SCHEMBL614446 0.80 EPHX1 (0.53) EPHX1SCN4AANPEPSIGMAR1TACR1
Benzylamine SCHEMBL8464424 0.79 LOXL2 (0.52) SIGMAR1SLC6A2TAAR1MAOASLC6A4
Hydrochloric Acid SCHEMBL5567986 0.79 EPHX1 (0.73) EPHX1SCN4AANPEPSIGMAR1SLC6A2
Hydrochloric Acid SCHEMBL18547947 0.79 EPHX1 (0.73) EPHX1SCN4AANPEPSIGMAR1SLC6A2
Benzylamine SCHEMBL18151475 0.78 LOXL2 (0.50) SIGMAR1SLC6A2TAAR1MAOASLC6A4
Hydrochloric Acid SCHEMBL20896980 0.78 EPHX1 (0.47) EPHX1SCN4AANPEPSIGMAR1TACR1
SCHEMBL137074 0.77 EPHX1 (0.76) EPHX1SCN4AANPEPSIGMAR1SLC6A2
SCHEMBL3441656 0.77 EPHX1 (0.76) EPHX1SCN4AANPEPSIGMAR1SLC6A2
SCHEMBL243771 0.77 EPHX1 (0.76) EPHX1SCN4AANPEPSIGMAR1SLC6A2

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2853546-B1 Modified starch compositions, starch composite foam materials and method for preparing the starch composite foam material IND TECH RES INST (TW) 2016-05-25 EP claimed
EP-2853546-A1 Modified starch compositions, starch composite foam materials and method for preparing the starch composite foam material Industrial Technology Research Institute (TW) 2015-04-01 EP claimed
US-20150065591-A1 MODIFIED STARCH COMPOSITIONS, STARCH COMPOSITE FOAM MATERIALS AND METHOD FOR PREPARING THE STARCH COMPOSITE FOAM MATERIAL INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2015-03-05 US claimed
EP-1945750-A2 MICROARRAY HAVING A BASE CLEAVABLE SUCINATE LINKER Combimatrix Corporation (US) 2008-07-23 EP claimed
US-20080125327-A1 Bonding amino moieties to solid surface with reactive hydroxyl groups, bonding succinate moieties to the amine groups through amide bonds to form cleavable linkers attached to the solid surface, bonding a succinate group, a sugar group and a base group, synthesizing oligonucleotides CUSTOMARRAY, INC. 2008-05-29 US claimed
WO-2007035500-A2 MICROARRAY HAVING A BASE CLEAVABLE SUCCINATE LINKER COMBIMATRIX CORPORATION (US) 2007-03-29 WO claimed
US-20070065877-A1 Microarray having a base cleavable succinate linker COMBIMATRIX CORPORATION 2007-03-22 US claimed
US-10428265-B2 Selective acidizing of a subterranean formation HALLIBURTON ENERGY SERVICES, INC. (US) 2019-10-01 US disclosed
US-20190227060-A1 MICROARRAY HAVING A BASE CLEAVABLE LINKER CUSTOMARRAY, INC. (US) 2019-07-25 US disclosed
US-10261075-B2 Microarray having a base cleavable linker CUSTOMARRAY, INC. (US) 2019-04-16 US disclosed
US-20180267032-A1 Microarray Having a Base Cleavable Linker CUSTOMARRAY, INC. (US) 2018-09-20 US disclosed
US-9983204-B2 Microarray having a base cleavable linker CUSTOMARRAY, INC. (US) 2018-05-29 US disclosed
US-9850362-B2 Modified starch compositions, starch composite foam materials and method for preparing the starch composite foam material INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2017-12-26 US disclosed
US-7461697-B2 Methods of modifying particulate surfaces to affect acidic sites thereon HALLIBURTON ENERGY SERVICES, INC. (US) 2008-12-09 US disclosed
EP-1945750-A2 MICROARRAY HAVING A BASE CLEAVABLE SUCINATE LINKER Combimatrix Corporation (US) 2008-07-23 EP disclosed
US-20080125327-A1 Bonding amino moieties to solid surface with reactive hydroxyl groups, bonding succinate moieties to the amine groups through amide bonds to form cleavable linkers attached to the solid surface, bonding a succinate group, a sugar group and a base group, synthesizing oligonucleotides CUSTOMARRAY, INC. 2008-05-29 US disclosed
US-20070114030-A1 Methods of modifying particulate surfaces to affect acidic sites thereon HALLIBURTON ENERGY SERVICES, INC. 2007-05-24 US disclosed
WO-2007057700-A1 METHODS OF MODIFYING PARTICULATE SURFACES TO AFFECT ACIDIC SITES THEREON HALLIBURTON ENERGY SERVICE, INC. (US) 2007-05-24 WO disclosed
WO-2007035500-A2 MICROARRAY HAVING A BASE CLEAVABLE SUCCINATE LINKER COMBIMATRIX CORPORATION (US) 2007-03-29 WO disclosed
US-20070065877-A1 Microarray having a base cleavable succinate linker COMBIMATRIX CORPORATION 2007-03-22 US disclosed