Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2250378

CCOC(=O)COc1cc(C)c(CCN[C@@H](C)[C@H](O)c2ccc(O)cc2)cc1C.Cl

nearest known ligand 0.68

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 15)

geneUniProtsupporting neighboursconfidence
ADRB3 known ✓ P13945 7/20 0.68
SLC6A2 known ✓ P23975 2/20 0.48
SLC6A4 known ✓ P31645 2/20 0.48
OPRM1 known ✓ P35372 2/20 0.48
SIGMAR1 known ✓ Q99720 1/20 0.48
ADRB2 known ✓ P07550 2/20 0.46
ADRB1 known ✓ P08588 1/20 0.46
ADRA1A known ✓ P35348 1/20 0.46
OPRK1 known ✓ P41145 1/20 0.46
SLC6A3 known ✓ Q01959 1/20 0.46
LMNA P02545 2/20 0.48
HIF1A Q16665 2/20 0.48
TMEM97 Q5BJF2 1/20 0.48
CYP2D6 P10635 1/20 0.46
GALR3 O60755 1/20 0.46

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 SCHEMBL4608896 1.00 ADRB3 (0.68) ADRB3LMNASLC6A2SLC6A4OPRM1
SCHEMBL14307655 0.99 ADRB3 (0.68) ADRB3LMNASLC6A2SLC6A4OPRM1
SCHEMBL3027520 0.99 ADRB3 (0.68) ADRB3LMNASLC6A2SLC6A4OPRM1
SCHEMBL2250255 0.99 ADRB3 (0.68) ADRB3LMNASLC6A2SLC6A4OPRM1
SCHEMBL6814376 0.91 ADRB3 (0.75) ADRB3LMNASLC6A2SLC6A4OPRM1
SCHEMBL6814366 0.91 ADRB3 (0.75) ADRB3LMNASLC6A2SLC6A4OPRM1
Ritobegron SCHEMBL2947591 0.89 ADRB3 (0.63) ADRB3LMNASLC6A2SLC6A4OPRM1
Ritobegron SCHEMBL2950593 0.89 ADRB3 (0.63) ADRB3LMNASLC6A2SLC6A4OPRM1
Ritobegron SCHEMBL2949688 0.89 ADRB3 (0.63) ADRB3LMNASLC6A2SLC6A4OPRM1
Ritobegron SCHEMBL2950589 0.89 ADRB3 (0.63) ADRB3LMNASLC6A2SLC6A4OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1620085-B1 USE OF PHENOXYACETIC ACID DERIVATIVES FOR TREATING HYPERACTIVE BLADDER KISSEI PHARMACEUTICAL (JP) 2008-07-23 EP claimed
EP-1620085-A1 USE OF PHENOXYACETIC ACID DERIVATIVES FOR TREATING HYPERACTIVE BLADDER Kissei Pharmaceutical Co., Ltd. (JP) 2006-02-01 EP claimed
US-20050154041-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and alpha-agonist BOEHRINGER INGELHEIN INTERNATIONAL GMBH (DE) 2005-07-14 US claimed
US-20050119239-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and an active substance which influences prostaglandin metabolism BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-06-02 US claimed
US-20050101607-A1 Pharmaceutical composition containing a beta-3-adrenoceptor agonist and an alpha antagonist and/or a 5-alpha reductase inhibitor BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-05-12 US claimed
WO-2004098586-A1 USE OF PHENOXYACETIC ACID DERIVATIVES FOR TREATING HYPERACTIVE BLADDER KISSEI PHARMACEUTICAL CO., LTD. (JP) 2004-11-18 WO claimed
US-20040229947-A1 Method of treating hyperactive bladder using phenoxyacetic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. 2004-11-18 US claimed
US-20170348288-A1 DOSING REGIMENS FOR BETA-3 ADRENOCEPTOR AGONISTS AND ANTI-MUSCARINIC AGENTS FOR THE TREATMENT AND PREVENTION OF LOWER URINARY TRACT SYMPTOMS AND OVERACTIVE BLADDER OXFORD FINANCE LLC, AS COLLATERAL AGENT 2017-12-07 US disclosed
US-8772315-B2 Pharmaceutical composition for treating overactive bladder ASTELLAS PHARMA INC. (JP) 2014-07-08 US disclosed
US-20130150402-A1 PHARMACEUTICAL COMPOSITION FOR TREATING OVERACTIVE BLADDER ASTELLAS PHARMA INC. (JP) 2013-06-13 US disclosed
EP-2216021-B1 PHARMACEUTICAL COMPOSITION FOR TREATING OVERACTIVE BLADDER ASTELLAS PHARMA INC (JP) 2012-10-17 EP disclosed
US-8003694-B2 Crystal of hydroxynorephedrin derivative hydrochloride ¼ hydrate KISSEI PHARMACEUTICAL CO., LTD. (JP) 2011-08-23 US disclosed
US-20100240697-A1 PHARMACEUTICAL COMPOSITION FOR TREATING OVERACTIVE BLADDER ASTELLAS PHARMA INC. (JP) 2010-09-23 US disclosed
US-20050154041-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and alpha-agonist BOEHRINGER INGELHEIN INTERNATIONAL GMBH (DE) 2005-07-14 US disclosed
US-20050119239-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and an active substance which influences prostaglandin metabolism BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-06-02 US disclosed
WO-2005042021-A2 PHARMACEUTICAL COMPOSITION, CONTAINING A BETA-3-ADRENOCEPTOR AGONIST AND AN ALPHA ANTAGONIST AND/OR A 5-ALPHA-REDUCTASE INHIBITOR BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-05-12 WO disclosed
US-20050101607-A1 Pharmaceutical composition containing a beta-3-adrenoceptor agonist and an alpha antagonist and/or a 5-alpha reductase inhibitor BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-05-12 US disclosed
US-20040242686-A1 Crystals of hydroxynorephedrine derivative KISSEI PHARMACEUTICAL CO. LTD. (JP) 2004-12-02 US disclosed
WO-2004098586-A1 USE OF PHENOXYACETIC ACID DERIVATIVES FOR TREATING HYPERACTIVE BLADDER KISSEI PHARMACEUTICAL CO., LTD. (JP) 2004-11-18 WO disclosed
US-20040229947-A1 Method of treating hyperactive bladder using phenoxyacetic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. 2004-11-18 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050101607-A1 Pharmaceutical composition containing a beta-3-adrenoceptor agonist and an alpha antagonist and/or a 5-alpha reductase inhibitor ADRB1, ADRB3, ADRB2 ADRB3 2/4885SLC6A2 589/4885SLC6A4 1138/4885
US-20050154041-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and alpha-agonist ADRB3, ADRB2, ADRB1 ADRB3 1/4885SLC6A2 257/4885SLC6A4 862/4885
US-20040229947-A1 Method of treating hyperactive bladder using phenoxyacetic acid derivatives BPHL, HTR5A, PNMT ADRB3 123/4885SLC6A2 15/4885SLC6A4 85/4885
US-20050119239-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and an active substance which influences prostaglandin metabolism ADRB3, ADRB2, ADRB1 ADRB3 1/4885SLC6A2 497/4885SLC6A4 1017/4885
US-20130150402-A1 PHARMACEUTICAL COMPOSITION FOR TREATING OVERACTIVE BLADDER BPHL, PDE12, UROD ADRB3 27/4885SLC6A2 846/4885SLC6A4 1600/4885
US-20100240697-A1 PHARMACEUTICAL COMPOSITION FOR TREATING OVERACTIVE BLADDER BPHL, PDE12, UROD ADRB3 23/4885SLC6A2 1015/4885SLC6A4 2087/4885
US-20040242686-A1 Crystals of hydroxynorephedrine derivative ADRA2C, ADRB2, ADRA2A ADRB3 9/4885SLC6A2 151/4885SLC6A4 301/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.