Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3719334

Cc1ccc(N2CCNCC2)cc1.Cl

nearest known ligand 0.96

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
ADRB1 known ✓ P08588 9/20 0.96
HTR3A known ✓ P46098 4/20 0.61
HTR3E known ✓ A5X5Y0 3/20 0.61
HTR3B known ✓ O95264 3/20 0.61
HTR3D known ✓ Q70Z44 3/20 0.61
HTR3C known ✓ Q8WXA8 3/20 0.61
SIGMAR1 known ✓ Q99720 3/20 0.61
ADRB2 known ✓ P07550 1/20 0.55
KCNH2 known ✓ Q12809 1/20 0.54
HTR1A known ✓ P08908 2/20 0.51
HTR1D known ✓ P28221 1/20 0.51
HTR1B known ✓ P28222 1/20 0.51
HTR7 known ✓ P34969 1/20 0.51
HTR2B known ✓ P41595 1/20 0.51
HTR5A known ✓ P47898 1/20 0.51
HTR6 known ✓ P50406 1/20 0.51
NCF1 P14598 1/20 0.55
PLD1 Q13393 1/20 0.55
ESRRB O95718 2/20 0.54
ESRRG P62508 2/20 0.54

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 SCHEMBL314404 1.00 ADRB1 (0.96) ADRB1HTR3AHTR3EHTR3BHTR3D
SCHEMBL81940 0.98 ADRB1 (1.00) ADRB1HTR3AHTR3EHTR3BHTR3D
SCHEMBL6645952 0.98 ADRB1 (1.00) ADRB1HTR3AHTR3EHTR3BHTR3D
Water SCHEMBL27430691 0.94 ADRB1 (0.92) ADRB1HTR3AHTR3EHTR3BHTR3D
Dimethylamine SCHEMBL28750709 0.92 ADRB1 (0.88) ADRB1HTR3AHTR3EHTR3BHTR3D
SCHEMBL82301 0.90 ADRB1 (0.85) ADRB1HTR3AHTR3EHTR3BHTR3D
Bicarbonate SCHEMBL11620170 0.88 ADRB1 (0.81) ADRB1HTR3AHTR3EHTR3BHTR3D
SCHEMBL7136974 0.87 ADRB1 (0.79) ADRB1HTR3AHTR3EHTR3BHTR3D
SCHEMBL21548392 0.87 ADRB1 (0.79) ADRB1HTR3AHTR3EHTR3BHTR3D
SCHEMBL2881718 0.87 ADRB1 (0.79) ADRB1HTR3AHTR3EHTR3BHTR3D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103328449-A Novel tetrahydroquinoline derivatives HOFFMANN LA ROCHE 2013-09-25 CN disclosed
CN-102382032-A 1-(phenyl)-4-[3-(4-indoxyl)-2-hydroxypropyl]piperazine derivative and salts thereof as well as preparation method and application thereof UNIV GUANGZHOU MEDICAL 2012-03-21 CN disclosed
US-7666865-B2 for treating pain; STROKES; ANALGESICS; do not contain substituents that are antioxidants, tropolones or coumarins NEUROMED PHARMACEUTICALS LTD. (CA) 2010-02-23 US disclosed
CN-100491357-C Benzimidazole compound and its preparing method and use in medicine production UNIV CHINA PHARMA (CN) 2009-05-27 CN disclosed
CN-1944416-A Benzimidazole compound and its preparing method and use in medicine production CHINA UNIV OF PHARMACY (CN) 2007-04-11 CN disclosed
US-20050256167-A1 Preparation and use of imidazole derivatives for treatment of obesity BAYER PHARMACEUTICALS CORPORATION (US) 2005-11-17 US disclosed
US-6960601-B2 Preparation and use of imidazole derivatives for treatment of obesity BAYER PHARMACEUTICALS CORPORATION (US) 2005-11-01 US disclosed
WO-2005099705-A2 PREPARATION OF IMIDAZOLE DERIVATIVES AND METHODS OF USE BAYER PHARMACEUTICALS CORPORATION (US) 2005-10-27 WO disclosed
US-20040063691-A1 Preparation and use of imidazole derivatives for treatment of obesity BAYER PHARMACEUTICALS CORPORATION 2004-04-01 US disclosed
EP-1205473-A1 VESAMICOL PIPERAZINE DERIVATIVES AND DRUGS CONTAINING THE SAME DAIICHI RADIOISOTOPE LABORATORIES, LTD. (JP) 2002-05-15 EP disclosed
EP-0609031-B1 Process for preparing benzothiazepine derivatives SHIONOGI & CO (JP) 1997-08-13 EP disclosed
US-5473066-A Cyclization, acetylation, hydrolysis, stereoselectivity SHIONOGI & CO., LTD. (JP) 1995-12-05 US disclosed
EP-0609031-A1 Process for preparing benzothiazepine derivatives SHIONOGI & CO., LTD. (JP) 1994-08-03 EP 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 (2 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-20040063691-A1 Preparation and use of imidazole derivatives for treatment of obesity GPR119, GIPR, PGC ADRB1 300/4885HTR3A 466/4885HTR3E 201/4885
US-20050256167-A1 Preparation and use of imidazole derivatives for treatment of obesity GPR119, GIPR, PGC ADRB1 300/4885HTR3A 466/4885HTR3E 201/4885

“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.