Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7264168

CCCCCCCCCCCCCC(N)c1ccccc1.Cl

nearest known ligand 0.63

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 10)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 1/20 0.47
CA2 known ✓ P00918 1/20 0.45
SIGMAR1 known ✓ Q99720 1/20 0.42
OPRM1 known ✓ P35372 2/20 0.41
OPRD1 known ✓ P41143 2/20 0.41
OPRK1 known ✓ P41145 2/20 0.41
SLC2A1 P11166 1/20 0.63
CSNK1E P49674 1/20 0.50
NAAA Q02083 2/20 0.41
OPRL1 P41146 2/20 0.41

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
Hydrochloric Acid SCHEMBL11865537 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
Hydrochloric Acid SCHEMBL11587424 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
Hydrochloric Acid SCHEMBL6676747 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
Hydrochloric Acid SCHEMBL4618375 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
Hydrochloric Acid SCHEMBL1109935 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
Hydrochloric Acid SCHEMBL1160867 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
Hydrochloric Acid SCHEMBL2313878 1.00 SLC2A1 (0.63) SLC2A1CSNK1EHTR2ACA2SIGMAR1
SCHEMBL4080852 0.98 SLC2A1 (0.60) SLC2A1CSNK1EHTR2ACA2SIGMAR1
SCHEMBL7734329 0.98 SLC2A1 (0.60) SLC2A1CSNK1EHTR2ACA2SIGMAR1
SCHEMBL10589876 0.98 SLC2A1 (0.60) SLC2A1CSNK1EHTR2ACA2SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 US claimed
US-4574158-A Acetal purification using phase transfer catalysts CONOCO INC. (US) 1986-03-04 US claimed
US-4513144-A Acetal purification with superoxides CONOCO INC. (US) 1985-04-23 US claimed
US-4412065-A Poly(oxy(silylene) esters) CONOCO INC. (US) 1983-10-25 US claimed
US-4379766-A Silyl esters of carboxylic acids by phase transfer catalysts CONOCO INC. (US) 1983-04-12 US claimed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 US claimed
EP-4342957-B1 OIL-RESISTANT AGENT DAIKIN IND LTD (JP) 2025-09-03 EP disclosed
US-12257567-B2 Process for preparation of superabsorbent polymer UPL LTD (IN) 2025-03-25 US disclosed
EP-4342957-A1 OIL-RESISTANT AGENT DAIKIN INDUSTRIES, LTD. (JP) 2024-03-27 EP disclosed
US-20220097022-A1 A PROCESS FOR PREPARATION OF SUPERABSORBENT POLYMER UPL LTD (IN) 2022-03-31 US disclosed
EP-3917996-A1 A PROCESS FOR PREPARATION OF SUPERABSORBENT POLYMER UPL Ltd (IN) 2021-12-08 EP disclosed
US-11072723-B2 Surface treatment agent DAIKIN INDUSTRIES, LTD. (JP) 2021-07-27 US disclosed
US-11034785-B2 Copolymer, and surface treatment agent DAIKIN INDUSTRIES, LTD. (JP) 2021-06-15 US disclosed
US-4379766-A Silyl esters of carboxylic acids by phase transfer catalysts CONOCO INC. (US) 1983-04-12 US disclosed
EP-0001825-B1 METHOD OF PREPARING 2,4-DIFLUOROANILINE MERCK & CO. INC. (US) 1982-01-13 EP disclosed
EP-0025846-A1 Improved process for the preparation of vinylcyclopropane derivatives NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1981-04-01 EP disclosed
US-4252739-A ALKYLATING AGENT SUCH AS 1,4-DIHALO-2-BUTENE, AN ACTIVE METHYLENE COMPOUND, A CATALYTIC ONIUM COMPOUND, AN ALKALI METAL COMPOUND AND WATER; ONE STEP EMERY INDUSTRIES, INC. (US) 1981-02-24 US disclosed
EP-0001825-A1 Method of preparing 2,4-difluoroaniline MERCK & CO. INC. (US) 1979-05-16 EP disclosed
US-4140719-A Solid-liquid phase transfer catalysis improved method of preparing 2,4-difluoroaniline MERCK & CO., INC. (US) 1979-02-20 US disclosed
US-3992432-A Phase transfer catalysis of heterogeneous reactions by quaternary salts CONTINENTAL OIL COMPANY (US) 1976-11-16 US disclosed