Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1438899

CS(=O)(=O)Oc1ccc(-c2sc3cc(OS(C)(=O)=O)ccc3c2C(=O)c2ccc(OCCN3CCCCC3)cc2)cc1.Cl

nearest known ligand 0.85

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
ESR1 known ✓ P03372 9/20 0.82
ESR2 known ✓ Q92731 7/20 0.77
ADRA2A known ✓ P08913 1/20 0.71
ADRB3 known ✓ P13945 1/20 0.71
DRD2 known ✓ P14416 1/20 0.71
ADRA2B known ✓ P18089 1/20 0.71
ADRA2C known ✓ P18825 1/20 0.71
DRD1 known ✓ P21728 1/20 0.71
ACHE known ✓ P22303 1/20 0.71
SLC6A2 known ✓ P23975 1/20 0.71
HRH2 known ✓ P25021 1/20 0.71
ADRA1D known ✓ P25100 1/20 0.71
HTR2A known ✓ P28223 1/20 0.71
HTR2C known ✓ P28335 1/20 0.71
SLC6A4 known ✓ P31645 1/20 0.71
ADRA1A known ✓ P35348 1/20 0.71
PTGS2 known ✓ P35354 1/20 0.71
OPRM1 known ✓ P35372 1/20 0.71
DRD3 known ✓ P35462 1/20 0.71
OPRD1 known ✓ P41143 1/20 0.71

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
SCHEMBL1439001 0.99 ENPP3 (0.87) ENPP3ESR1STSENPP1ESR2
SCHEMBL10827879 0.99 ENPP3 (0.87) ENPP3ESR1STSENPP1ESR2
SCHEMBL10827744 0.98 ENPP3 (0.85) ENPP3ESR1STSENPP1ESR2
SCHEMBL8596738 0.94 ENPP3 (0.79) ENPP3ESR1STSENPP1ESR2
SCHEMBL6836622 0.94 ENPP3 (0.78) ENPP3ESR1STSENPP1ESR2
SCHEMBL4608181 0.93 STS (0.84) ENPP3ESR1STSESR2MEN1
SCHEMBL10828093 0.90 ENPP3 (0.73) ENPP3ESR1STSENPP1ESR2
Hydrochloric Acid SCHEMBL8388923 0.89 ENPP3 (0.83) ENPP3ESR1STSENPP1ESR2
SCHEMBL18872885 0.89 ESR1 (0.81) ENPP3ESR1STSENPP1ESR2
SCHEMBL10827833 0.88 ENPP3 (0.85) ENPP3ESR1STSENPP1ESR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2011029088-A3 PREPARATION OF RALOXIFENE AND ITS SALTS DR. REDDY'S LABORATORIES LTD. (IN) 2011-11-24 WO disclosed
WO-2011029088-A2 PREPARATION OF RALOXIFENE AND ITS SALTS DR. REDDY'S LABORATORIES LTD. (IN) 2011-03-10 WO disclosed
WO-2011029088-A2 PREPARATION OF RALOXIFENE AND ITS SALTS DR. REDDY'S LABORATORIES LTD. (IN) 2011-03-10 WO disclosed
WO-2009008000-A2 A PROCESS FOR THE PREPARATION OF 6-HYDROXY-2-(4-HYDROXYPHENYL)-3-[4-(2-PIPERIDINO ETHOXY) BENZOYL]BENZO[B]THIOPHENE SUN PHARMACEUTICAL INDUSTRIES LTD. (IN) 2009-01-15 WO disclosed
US-5994371-A OSTEOPOROSIS; ANTICHOLESTEROL AGENT; ANTICANCER AGENT FORMAMMARY GLAND, UTERINE CANCER ELI LILLY AND COMPANY (US) 1999-11-30 US disclosed
EP-0617030-B1 Sulfonate and carbamate derivatives of 3-aroylbenzo (beta) thiophenes LILLY CO ELI (US) 1999-05-26 EP disclosed
US-5605924-A USEFUL IN PREVENTING BONE LOSS, TREATING HYPERCHOLESTEREMIA AND TREATING HORMONE DEPENDENT MAMMALIAN BREAST AND UTERINE CARCINOMA ELI LILLY AND COMPANY (US) 1997-02-25 US disclosed
US-5599833-A ANTICARCER AGENT, OSTEOPOROSIS, ANTICHOLESTEROL AGENT ELI LILLY AND COMPANY (US) 1997-02-04 US disclosed
US-5482949-A INHIBITING BONE LOSS, LOWERING CHOLESTEROL LEVELS, AND TREATING ESTROGEN DEPENDENT MAMMARY OR UTERINE CARCINOMA ELI LILLY AND COMPANY (US) 1996-01-09 US disclosed
EP-0617030-A1 Sulfonate and carbamate derivatives of 3-aroylbenzo (beta) thiophenes ELI LILLY AND COMPANY (US) 1994-09-28 EP disclosed