Hydrochloric Acid

Hydrochloric Acid

SCHEMBL767526

CC(C)CCCCCCCCCCCNCc1ccccc1.Cl

nearest known ligand 0.69

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 15)

geneUniProtsupporting neighboursconfidence
MAOA known ✓ P21397 1/20 0.69
CHRM2 known ✓ P08172 2/20 0.67
SIGMAR1 known ✓ Q99720 4/20 0.61
GAA known ✓ P10253 1/20 0.52
HDAC3 known ✓ O15379 1/20 0.50
HDAC1 known ✓ Q13547 1/20 0.50
HDAC2 known ✓ Q92769 1/20 0.50
HDAC8 known ✓ Q9BY41 1/20 0.50
ACHE known ✓ P22303 3/20 0.48
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
MAPT P10636 1/20 0.52
NCOR2 Q9Y618 1/20 0.50
FOLH1 Q04609 1/20 0.48

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 SCHEMBL199811 1.00 MAOA (0.69) MAOACHRM2SIGMAR1MEN1KMT2A
Hydrochloric Acid SCHEMBL2790069 1.00 MAOA (0.69) MAOACHRM2SIGMAR1MEN1KMT2A
Hydrochloric Acid SCHEMBL2789724 1.00 MAOA (0.69) MAOACHRM2SIGMAR1MEN1KMT2A
Hydrochloric Acid SCHEMBL28399413 1.00 MAOA (0.69) MAOACHRM2SIGMAR1MEN1KMT2A
Hydrochloric Acid SCHEMBL10584193 1.00 MAOA (0.69) MAOACHRM2SIGMAR1MEN1KMT2A
Hydrochloric Acid SCHEMBL2365614 0.98 MAOA (0.67) MAOACHRM2SIGMAR1MEN1KMT2A
SCHEMBL7861380 0.98 MAOA (0.71) MAOACHRM2SIGMAR1MEN1KMT2A
SCHEMBL29380563 0.98 MAOA (0.71) MAOACHRM2SIGMAR1MEN1KMT2A
SCHEMBL372804 0.98 MAOA (0.71) MAOACHRM2SIGMAR1MEN1KMT2A
SCHEMBL640522 0.98 MAOA (0.71) MAOACHRM2SIGMAR1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050036904-A1 Methods for eradication of nanobacteria KAJANDER OLAVI E (FI) 2005-02-17 US claimed
US-6827959-B1 Quaternary onium having long chain alkyl and aromatic functionality modified phyllosilicates; purifying cereals, grains and animal feeds; adsorbs both aflatoxins and nonaflatoxins; low cost SUD-CHEMIE AG (DE) 2004-12-07 US claimed
EP-1094711-B1 METHODS FOR ERADICATION OF NANOBACTERIA NANOBAC OY (FI) 2004-11-24 EP claimed
US-6706290-B1 CALCIUM CHELATION DEMINERALIZATION THEN DISINFECTING; PREVENTING KIDNEY, SALIVARY GLAND AND DENTAL PULP STONES AND ATHEROSCLEROSIS CIFTCIOGLU, NEVA DR. 2004-03-16 US claimed
EP-1094711-A1 METHODS FOR ERADICATION OF NANOBACTERIA Kajander, E. Olavi (FI) 2001-05-02 EP claimed
WO-2000001238-A1 METHODS FOR ERADICATION OF NANOBACTERIA KAJANDER E OLAVI (FI) 2000-01-13 WO claimed
US-5243110-A DEHYDROCHLORINATION OF 1,1-BIS(R-PHENYL)-2,2,2-TRICHLOROETHANES ELF ATOCHEM S.A. (FR) 1993-09-07 US claimed
JP-9316776-A None JP disclosed
JP-58076517-A None JP disclosed
EP-2363498-B1 METHOD FOR QUANTITATIVELY DETERMINING CHOLESTEROL IN LOW-DENSITY LIPOPROTEINS, REAGENT FOR QUANTITATIVE DETERMINATION, AND QUANTITATIVE DETERMINATION KIT KYOWA MEDEX CO LTD (JP) 2016-05-25 EP disclosed
US-8344175-B2 Liquid crystal compositions, polymer networks derived therefrom and process for making the same E I DU PONT DE NEMOURS AND COMPANY (US) 2013-01-01 US disclosed
US-8334393-B2 Chiral compounds and liquid crystal compositions and polymer networks derived therefrom E I DU PONT DE NEMOURS AND COMPANY (US) 2012-12-18 US disclosed
US-20120219683-A1 TOXIN ADSORBENT SUD-CHEMIE AG (DE) 2012-08-30 US disclosed
EP-0003835-B1 A HYDROXY-UREA, PROCESS FOR PRODUCING THE SAME AND A PROCESS FOR PRODUCING A PHENYL-SUBSTITUTED N-METHOXY-N-METHYL-UREA SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1983-03-02 EP disclosed
EP-0063872-A1 Process for the preparation of fluoromethyl pyridines and certain novel products obtained therefrom IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1982-11-03 EP disclosed
US-4328166-A Production of substituted phenylurea SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1982-05-04 US disclosed
US-4263219-A METHYLATION IN TWO-PHASE REACTION MEDIUM SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1981-04-21 US disclosed
US-4172782-A ORGANIC QUATERNARY AMMONIUM SALT USED IN ALKULATION OF BENZYLNITRILE WITH AN ORGANIC HALIDE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1979-10-30 US disclosed
US-4159994-A AMMONIUM OR ALKALI METAL CARBOXYLATE UNIBRA SOCIETE ANONYME (BE) 1979-07-03 US disclosed
US-4153624-A FROM A UREA AND NITROUS ACID, SOLVENTS, PHASE TRANSFER AGENTS IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1979-05-08 US disclosed