Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6684814

COc1ccc(CC(C)N)cc1S(N)(=O)=O.Cl

nearest known ligand 0.62

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
ADRA1D known ✓ P25100 6/20 0.54
ADRA1A known ✓ P35348 6/20 0.54
ADRA1B known ✓ P35368 6/20 0.54
ADRB2 known ✓ P07550 1/20 0.54
ADRB1 known ✓ P08588 1/20 0.54
HTR1A known ✓ P08908 1/20 0.54
ADRA2A known ✓ P08913 1/20 0.54
DRD2 known ✓ P14416 1/20 0.54
ADRA2B known ✓ P18089 1/20 0.54
ADRA2C known ✓ P18825 1/20 0.54
HTR2A known ✓ P28223 1/20 0.54
HTR7 known ✓ P34969 1/20 0.54
OPRM1 known ✓ P35372 1/20 0.54
DRD3 known ✓ P35462 1/20 0.54
HTR2B known ✓ P41595 1/20 0.54
KCNH2 known ✓ Q12809 1/20 0.54
SLC6A4 known ✓ P31645 1/20 0.46
PKM P14618 1/20 0.49
TAAR1 Q96RJ0 2/20 0.46
ALOX15 P16050 1/20 0.45

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 SCHEMBL3939257 1.00 ADRA1D (0.54) ADRA1DADRA1AADRA1BADRB2ADRB1
SCHEMBL1412240 0.98 ADRA1D (0.55) ADRA1DADRA1AADRA1BADRB2ADRB1
SCHEMBL29519545 0.98 ADRA1D (0.55) ADRA1DADRA1AADRA1BADRB2ADRB1
SCHEMBL1412238 0.98 ADRA1D (0.55) ADRA1DADRA1AADRA1BADRB2ADRB1
SCHEMBL3948856 0.98 ADRA1D (0.55) ADRA1DADRA1AADRA1BADRB2ADRB1
SCHEMBL13880696 0.98 ADRA1D (0.55) ADRA1DADRA1AADRA1BADRB2ADRB1
Cadaverine Tartrate SCHEMBL3944116 0.88 PKM (0.51) ADRA1DADRA1AADRA1BADRB2ADRB1
Cadaverine Tartrate SCHEMBL3952300 0.88 PKM (0.51) ADRA1DADRA1AADRA1BADRB2ADRB1
SCHEMBL14368066 0.88 ADRA1D (0.56) ADRA1DADRA1AADRA1BADRB2ADRB1
Hydrochloric Acid SCHEMBL9634032 0.86 ADRA1D (0.52) ADRA1DADRA1AADRA1BADRB2ADRB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112824378-A Preparation method of tamsulosin hydrochloride 珠海润都制药股份有限公司 2021-05-21 CN disclosed
CN-111320559-A Preparation method of tamsulosin hydrochloride 苏州盛迪亚生物医药有限公司 2020-06-23 CN disclosed
WO-2019058290-A1 IMPROVED PROCESS FOR THE PREPARATION OF OZANIMOD Α-AMINO COMPOUND SUVEN LIFE SCIENCES LIMITED (IN) 2019-03-28 WO disclosed
WO-2004087623-A2 AN IMPROVED PROCESS FOR THE PREPARATION OF (R) (-) TAMSULOSIN HYDROCHLORIDE ALEMBIC LIMITED (IN) 2004-10-14 WO disclosed
EP-0380144-B1 Process for producing optically active benzene-sulfonamide derivatives YAMANOUCHI PHARMA CO LTD (JP) 1994-01-19 EP disclosed
EP-0380144-A1 Process for producing optically active benzene-sulfonamide derivatives YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 1990-08-01 EP disclosed
EP-0257787-A1 Process for producing optically active benzene-sulfonamide derivates YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 1988-03-02 EP disclosed