Hydrochloric Acid

Hydrochloric Acid

SCHEMBL724080

CC(N)Cc1ccccc1O.Cl

nearest known ligand 0.67

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
SLC6A2 known ✓ P23975 3/20 0.49
SLC6A4 known ✓ P31645 2/20 0.49
SLC6A3 known ✓ Q01959 2/20 0.49
ADRB1 known ✓ P08588 1/20 0.49
HTR1A known ✓ P08908 1/20 0.49
ADRA2A known ✓ P08913 1/20 0.49
HTR1D known ✓ P28221 1/20 0.49
HTR1B known ✓ P28222 1/20 0.49
HTR2A known ✓ P28223 1/20 0.49
HTR2C known ✓ P28335 1/20 0.49
HTR1E known ✓ P28566 1/20 0.49
HTR7 known ✓ P34969 1/20 0.49
HTR2B known ✓ P41595 1/20 0.49
HTR6 known ✓ P50406 1/20 0.49
MAOA known ✓ P21397 1/20 0.48
SIGMAR1 known ✓ Q99720 1/20 0.48
POLB P06746 1/20 0.49
MAPK1 P28482 1/20 0.49
IDO1 P14902 1/20 0.48
TAAR1 Q96RJ0 2/20 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
SCHEMBL4742791 0.98 SLC6A2 (0.50) SLC6A2SLC6A4SLC6A3ADRB1HTR1A
SCHEMBL266416 0.98 SLC6A2 (0.50) SLC6A2SLC6A4SLC6A3ADRB1HTR1A
SCHEMBL5914402 0.98 SLC6A2 (0.50) SLC6A2SLC6A4SLC6A3ADRB1HTR1A
Bromide SCHEMBL6052803 0.96 SLC6A2 (0.49) SLC6A2SLC6A4SLC6A3ADRB1HTR1A
Iodide SCHEMBL6052802 0.96 SLC6A2 (0.49) SLC6A2SLC6A4SLC6A3ADRB1HTR1A
SCHEMBL2857779 0.82 SLC6A2 (0.61) SLC6A2SLC6A4SLC6A3ADRB1HTR1A
SCHEMBL632694 0.82 GABRA1 (0.55) SLC6A2SLC6A4SLC6A3TAAR1MAOA
SCHEMBL19971988 0.82 CYP2D6 (0.47) SLC6A2SLC6A4SLC6A3POLBMAPK1
SCHEMBL3071437 0.80 HSPA5 (0.54) SLC6A2SLC6A4SLC6A3POLBIDO1
SCHEMBL108067 0.80 GABRA1 (0.64) POLBMAPK1IDO1TAAR1

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1480677-B8 COMPOSITION FOR STABILIZING HYALURONIC ACID CARL ZEISS MEDITEC SAS (FR) 2012-05-23 EP claimed
EP-1480677-B1 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2012-02-29 EP claimed
CN-102231969-A Macrocyclic lactone compounds and methods for their use ELIXIR MEDICAL CORP 2011-11-02 CN claimed
CN-102215682-A Macrolide compounds and methods of their use ELIXIR MEDICAL CORP 2011-10-12 CN claimed
EP-1480677-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2004-12-01 EP claimed
US-20030133986-A1 Compositions for stabilizing poly (carboxylic acids) TSAO FU-PAO (US) 2003-07-17 US claimed
WO-2003043660-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID NOVARTIS AG (CH) 2003-05-30 WO claimed
EP-1480677-B8 COMPOSITION FOR STABILIZING HYALURONIC ACID CARL ZEISS MEDITEC SAS (FR) 2012-05-23 EP disclosed
EP-1480677-B1 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2012-02-29 EP disclosed
CN-102231969-A Macrocyclic lactone compounds and methods for their use ELIXIR MEDICAL CORP 2011-11-02 CN disclosed
CN-102215682-A Macrolide compounds and methods of their use ELIXIR MEDICAL CORP 2011-10-12 CN disclosed
EP-1480677-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2004-12-01 EP disclosed
US-20030133986-A1 Compositions for stabilizing poly (carboxylic acids) TSAO FU-PAO (US) 2003-07-17 US disclosed
WO-2003043660-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID NOVARTIS AG (CH) 2003-05-30 WO disclosed