Hydrochloric Acid

Hydrochloric Acid

SCHEMBL534137

C=C(C)C(=O)OCC(O)C[N+](C)(C)C.Cl

nearest known ligand 0.57

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 20)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 3/20 0.38
CHRM4 known ✓ P08173 3/20 0.38
CHRM1 known ✓ P11229 3/20 0.38
CHRM5 known ✓ P08912 2/20 0.33
CHRM3 known ✓ P20309 2/20 0.33
HRH1 known ✓ P35367 1/20 0.33
HTR1A known ✓ P08908 1/20 0.32
CHRNB4 known ✓ P30926 1/20 0.32
CHRNA3 known ✓ P32297 1/20 0.32
CHRNA7 known ✓ P36544 1/20 0.32
TSHR P16473 5/20 0.57
THRB P10828 1/20 0.40
MAPT P10636 3/20 0.39
SLC22A16 Q86VW1 1/20 0.39
TBXA2R P21731 2/20 0.38
ALDH1A1 P00352 2/20 0.38
SMN1; SMN2 Q16637 3/20 0.37
GALR3 O60755 1/20 0.37
BLM P54132 1/20 0.37
LMNA P02545 3/20 0.33

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
SCHEMBL758619 0.98 TSHR (0.59) TSHRTHRBMAPTSLC22A16CHRM2
Hydrochloric Acid SCHEMBL6300759 0.96 TSHR (0.53) TSHRTHRBMAPTSLC22A16CHRM2
Iodide SCHEMBL1255392 0.96 TSHR (0.57) TSHRTHRBMAPTSLC22A16CHRM2
Hydrochloric Acid SCHEMBL204258 0.96 TSHR (0.57) TSHRTHRBMAPTSLC22A16CHRM2
Fluoride Ion SCHEMBL1254970 0.96 TSHR (0.57) TSHRTHRBMAPTSLC22A16CHRM2
Bromide SCHEMBL1254317 0.96 TSHR (0.57) TSHRTHRBMAPTSLC22A16CHRM2
Chloromethane SCHEMBL10796929 0.94 TSHR (0.55) TSHRTHRBMAPTSLC22A16CHRM2
Acetic Acid SCHEMBL22188618 0.93 TSHR (0.53) TSHRTHRBMAPTSLC22A16CHRM2
Sulfuric Acid SCHEMBL8098694 0.90 TSHR (0.50) TSHRTHRBMAPTSLC22A16CHRM2
Phosphoric Acid SCHEMBL8763237 0.90 TSHR (0.50) TSHRTHRBMAPTSLC22A16CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2264486-B1 Ophthalmic, tinted molding composition, molding having high Dk-value and method of its production NOVARTIS AG (CH) 2018-08-22 EP claimed
US-8361492-B2 Drug delivery system and methods of use Ocugenics, LLC (US) 2013-01-29 US claimed
EP-2413917-A2 DRUG DELIVERY SYSTEM AND METHODS OF USE Ocugenics, Llc (US) 2012-02-08 EP claimed
JP-4638127-B2 2011-02-23 JP claimed
EP-2264486-A2 Ophthalmic molding composition Novartis AG (CH) 2010-12-22 EP claimed
US-7847016-B2 Tinted, high DK ophthalmic molding and a method for making same NOVARTIS AG (CH) 2010-12-07 US claimed
WO-2010120489-A2 DRUG DELIVERY SYSTEM AND METHODS OF USE Ocugenics, LLC (US) 2010-10-21 WO claimed
US-20090269392-A1 Drug Delivery System And Methods Of Use Ocugenics, LLC 2009-10-29 US claimed
US-20090096985-A1 Tinted, high DK ophthalmic molding and a method for making same ALCON INC. (CH) 2009-04-16 US claimed
JP-2004517360-A 2004-06-10 JP claimed
EP-1360527-A2 A TINTED, HIGH DK OPHTHALMIC MOLDING AND A METHOD FOR MAKING SAME Novartis AG (CH) 2003-11-12 EP claimed
WO-2002054136-A2 A TINTED, HIGH DK OPHTHALMIC MOLDING AND A METHOD FOR MAKING SAME NOVARTIS AG (CH) 2002-07-11 WO claimed
EP-2951242-B1 WATER SOLUBLE SILICONE MATERIAL MOMENTIVE PERFORMANCE MAT INC (US) 2019-09-11 EP disclosed
US-10118994-B2 Water soluble silicone material MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2018-11-06 US disclosed
EP-2264486-B1 Ophthalmic, tinted molding composition, molding having high Dk-value and method of its production NOVARTIS AG (CH) 2018-08-22 EP disclosed
US-9956168-B2 Extended release drug-delivery contact lenses and methods of making MERCY MEDICAL RESEARCH INSTITUTE (US) 2018-05-01 US disclosed
EP-0819258-A1 EXTENDED WEAR OPHTHALMIC LENS Novartis AG (CH) 1998-01-21 EP disclosed
WO-1997022019-A1 METHODS OF MANUFACTURING CONTACT LENSES NOVARTIS AG (CH) 1997-06-19 WO disclosed
WO-1996036890-A1 POLYSILOXANE-POLYOL MACROMERS, THEIR PREPARATION AND THEIR USE NOVARTIS AG (CH) 1996-11-21 WO disclosed
WO-1996031792-A1 EXTENDED WEAR OPHTHALMIC LENS NOVARTIS AG (CH) 1996-10-10 WO disclosed