Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2957420

C=CCN(CC=C)C1CCCCC1.Cl

nearest known ligand 0.40

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 13)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 1/20 0.35
ALDH1A1 P00352 1/20 0.40
ADH1A P07327 8/20 0.34
ADH1C P00326 5/20 0.34
NOS1 P29475 1/20 0.32
NOS2 P35228 1/20 0.32
CYP2D6 P10635 2/20 0.32
CYP2C9 P11712 2/20 0.32
HSD17B10 Q99714 1/20 0.32
TSHR P16473 1/20 0.32
ADH4 P08319 1/20 0.31
ADH1B P00325 1/20 0.30
KDM4E B2RXH2 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
SCHEMBL30750 0.98 ALDH1A1 (0.41) ALDH1A1SIGMAR1ADH1AADH1CNOS1
Fluoride SCHEMBL9620616 0.95 ALDH1A1 (0.40) ALDH1A1SIGMAR1ADH1AADH1CCYP2D6
Ammonia Solution, Strong SCHEMBL17439397 0.95 ALDH1A1 (0.40) ALDH1A1SIGMAR1ADH1AADH1CCYP2D6
SCHEMBL2163192 0.95 ALDH1A1 (0.38) ALDH1A1SIGMAR1ADH1AADH1CNOS1
SCHEMBL10582372 0.88 ALDH1A1 (0.39) ALDH1A1ADH1AADH1CCYP2D6CYP2C9
SCHEMBL2363531 0.85 SIGMAR1 (0.35) SIGMAR1
SCHEMBL10975387 0.85 ALDH1A1 (0.37) ALDH1A1ADH1AADH1CNOS1NOS2
SCHEMBL3467156 0.85 ADH1A (0.44) ALDH1A1SIGMAR1ADH1AADH1CADH1B
SCHEMBL10716961 0.81 ALDH1A1 (0.42) ALDH1A1ADH1ACYP2D6CYP2C9HSD17B10
SCHEMBL3429552 0.81 ADH1A (0.47) ALDH1A1ADH1AADH1C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190217311-A1 CATIONIC POLYMER SELECTIVE DEPRESSANTS AND USE THEREOF IN MINERAL ORE PURIFICATION METHODS KEMIRA OYJ (FI) 2019-07-18 US claimed
EP-1759058-A1 METHOD FOR MANUFACTURING PAPER OR SIMILAR STFI-Packforsk AB (SE) 2007-03-07 EP claimed
WO-2005124020-A1 METHOD FOR MANUFACTURING PAPER OR SIMILAR STFI-PACKFORSK AB (SE) 2005-12-29 WO claimed
US-20050061750-A1 Methods for the purification of contaminated waters POLYMER VENTURES, INC. (US) 2005-03-24 US claimed
US-6361652-B2 ADDED WITH FLOCCULANT TO PAPERMAKING FURNISH AS RETENSION AID NALCO CHEMICAL COMPANY 2002-03-26 US claimed
US-20010030032-A1 Method of increasing retention in papermaking using colloidal borosilicates ECOLAB USA INC. 2001-10-18 US claimed
US-20010023752-A1 Method of increasing drainage in papermaking using colloidal borosilicates ECOLAB USA INC. 2001-09-27 US claimed
US-20010023753-A1 Method for flocculating a papermaking furnish using colloidal borosilicates ECOLAB USA INC. 2001-09-27 US claimed
US-6270627-B1 IN CONJUNCTION WITH A HIGH MOLECULAR WEIGHT SYNTHETIC FLOCCULANT AND/OR STARCH, WITH OR WITHOUT THE ADDITON OF A CATIONIC COAGULANT; IMPROVED LEVELS OF RETENTION, FORMATION, UNIFORM POROSITY, AND OVERALL DEWATERING NALCO CHEMICAL COMPANY 2001-08-07 US claimed
CN-1275116-A Colloidal borosilicates and their use in poduction of paper NALCO CHEMICAL CO (US) 2000-11-29 CN claimed
EP-1023241-A1 COLLOIDAL BOROSILICATES AND THEIR USE IN THE PRODUCTION OF PAPER NALCO CHEMICAL COMPANY (US) 2000-08-02 EP claimed
WO-1999016708-A1 COLLOIDAL BOROSILICATES AND THEIR USE IN THE PRODUCTION OF PAPER NALCO CHEMICAL COMPANY (US) 1999-04-08 WO claimed
US-4655934-A BASIC ALUMINUM HALIDE AS FLOCCULANTS TO CLARIFY WATER NALCO CHEMICAL COMPANY (US) 1987-04-07 US claimed
US-11926543-B2 Use of multiple charged ionic compounds derived from polyamines for waste water clarification ECOLAB USA INC. (US) 2024-03-12 US disclosed
US-11802376-B2 Paper strength improving additives, their manufacture and use in paper making KEMIRA OYJ (FI) 2023-10-31 US disclosed
US-11612898-B2 Cationic polymer selective depressants and use thereof in mineral ore purification methods KEMIRA OYJ (FI) 2023-03-28 US disclosed
EP-0773319-A1 Method to enhance the performance of polymers and copolymers of acrylamide as flocculants and retention aids NALCO CHEMICAL COMPANY (US) 1997-05-14 EP disclosed
US-4812540-A CONTAINING CATIONIC NITROGEN NITTO BOSEKI CO., LTD. (JP) 1989-03-14 US disclosed
EP-0140309-B1 PROCESS FOR THE PREPARATION OF COPOLYMERS OF MONOALLYLAMINE AND DIALLYLAMINE DERIVATIVES NITTO BOSEKI CO., LTD. (JP) 1988-10-19 EP disclosed
EP-0140309-A2 Process for the preparation of copolymers of monoallylamine and diallylamine derivatives NITTO BOSEKI CO., LTD. (JP) 1985-05-08 EP disclosed