Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3475007

Cl.O=C(c1ccc(OCCC2CCCCN2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12

nearest known ligand 0.66

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 20/20 0.66
ESR2 known ✓ Q92731 19/20 0.66
ADRA2A known ✓ P08913 1/20 0.65
ADRB3 known ✓ P13945 1/20 0.65
DRD2 known ✓ P14416 1/20 0.65
ADRA2B known ✓ P18089 1/20 0.65
ADRA2C known ✓ P18825 1/20 0.65
DRD1 known ✓ P21728 1/20 0.65
ACHE known ✓ P22303 1/20 0.65
SLC6A2 known ✓ P23975 1/20 0.65
HRH2 known ✓ P25021 1/20 0.65
ADRA1D known ✓ P25100 1/20 0.65
HTR2A known ✓ P28223 1/20 0.65
HTR2C known ✓ P28335 1/20 0.65
SLC6A4 known ✓ P31645 1/20 0.65
ADRA1A known ✓ P35348 1/20 0.65
PTGS2 known ✓ P35354 1/20 0.65
OPRM1 known ✓ P35372 1/20 0.65
DRD3 known ✓ P35462 1/20 0.65
OPRD1 known ✓ P41143 1/20 0.65

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
SCHEMBL5309771 0.99 ESR1 (0.67) ESR1ESR2MEN1ALDH1A1LMNA
1,2-Dichloroethane SCHEMBL6766354 0.97 ESR1 (0.62) ESR1ESR2MEN1ALDH1A1LMNA
SCHEMBL6763195 0.96 ESR1 (0.68) ESR1ESR2MEN1ALDH1A1LMNA
SCHEMBL6832617 0.90 ESR1 (0.61) ESR1ESR2MEN1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL6767144 0.89 ESR1 (0.67) ESR1ESR2MEN1ALDH1A1LMNA
SCHEMBL6773068 0.88 ESR1 (0.66) ESR1ESR2MEN1ALDH1A1LMNA
SCHEMBL6979219 0.86 ESR1 (0.70) ESR1ESR2MEN1ALDH1A1LMNA
SCHEMBL5706934 0.86 ESR1 (0.56) ESR1ESR2MEN1ALDH1A1LMNA
Hydrochloric Acid SCHEMBL7638256 0.85 ESR1 (0.65) ESR1ESR2MEN1ALDH1A1LMNA
SCHEMBL11185523 0.84 ESR1 (0.64) ESR1ESR2MEN1ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6713494-B1 SUCH AS 6-HYDROXY-2-(4-HYDROXYPHENYL)-3-(4-(2-PIPERIDINYL-ETHOXY)BENZOYL)BENZOTHIOPHENE HYDROCHLORIDE SALT; OSTEO-POROSIS ELI LILLY AND COMPANY 2004-03-30 US claimed
WO-2010145010-A1 TREATMENT OF HOT FLUSHES, VASOMOTOR SYMPTOMS, AND NIGHT SWEATS WITH SEX STEROID PRECURSORS IN COMBINATION WITH SELECTIVE ESTROGEN RECEPTOR MODULATORS ENDORECHERCHE, INC. (CA) 2010-12-23 WO disclosed
WO-2009049643-A1 IMPROVED PHARMACEUTICAL COMPOSITION CONTAINING A SELECTIVE ESTROGEN RECEPTOR MODULATOR AND METHOD FOR THE PREPARATION THEREOF PHARMATHEN S.A. (GR) 2009-04-23 WO disclosed
US-6713494-B1 SUCH AS 6-HYDROXY-2-(4-HYDROXYPHENYL)-3-(4-(2-PIPERIDINYL-ETHOXY)BENZOYL)BENZOTHIOPHENE HYDROCHLORIDE SALT; OSTEO-POROSIS ELI LILLY AND COMPANY 2004-03-30 US disclosed
EP-0826682-B1 Amorphous Bentothiophene, method of preparation and method of use. LILLY CO ELI (US) 2003-03-12 EP disclosed
EP-1251855-A1 SELECTIVE ESTROGEN RECEPTOR MODULATORS IN COMBINATION WITH ESTROGENS Endorecherche, Inc. (CA) 2002-10-30 EP disclosed
WO-2001054699-A1 SELECTIVE ESTROGEN RECEPTOR MODULATORS IN COMBINATION WITH ESTROGENS ENDORECHERCHE, INC. (CA) 2001-08-02 WO disclosed
EP-0826682-A1 Amorphous benzothiophenes, methods of preparation, and methods of use ELI LILLY AND COMPANY (US) 1998-03-04 EP disclosed