Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7266355

Cl.O=C(O)C=Cc1ccc(Cc2ncc[nH]2)cc1

nearest known ligand 0.54

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
HDAC8 known ✓ Q9BY41 3/20 0.45
HDAC3 known ✓ O15379 2/20 0.45
HDAC4 known ✓ P56524 2/20 0.45
HDAC1 known ✓ Q13547 2/20 0.45
HDAC7 known ✓ Q8WUI4 2/20 0.45
HDAC2 known ✓ Q92769 2/20 0.45
HDAC10 known ✓ Q969S8 2/20 0.45
HDAC11 known ✓ Q96DB2 2/20 0.45
HDAC6 known ✓ Q9UBN7 2/20 0.45
HDAC9 known ✓ Q9UKV0 2/20 0.45
HDAC5 known ✓ Q9UQL6 2/20 0.45
CA2 known ✓ P00918 1/20 0.42
ESR1 known ✓ P03372 1/20 0.42
DPP4 known ✓ P27487 1/20 0.42
ESR2 known ✓ Q92731 1/20 0.42
TBXAS1 P24557 6/20 0.54
TAAR1 Q96RJ0 2/20 0.54
CYP1A2 P05177 2/20 0.45
USP2 O75604 1/20 0.45
LMNA P02545 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 SCHEMBL10848541 0.99 TBXAS1 (0.53) TBXAS1TAAR1HDAC8HDAC3HDAC4
Hydrochloric Acid SCHEMBL11261045 0.99 TBXAS1 (0.53) TBXAS1TAAR1HDAC8HDAC3HDAC4
SCHEMBL9507338 0.99 TAAR1 (0.55) TBXAS1TAAR1HDAC8HDAC3HDAC4
SCHEMBL9401700 0.99 TAAR1 (0.55) TBXAS1TAAR1HDAC8HDAC3HDAC4
SCHEMBL11107735 0.83 CA12 (0.49) TAAR1HDAC8HDAC3HDAC4HDAC1
SCHEMBL11260195 0.82 CA12 (0.55) TAAR1HDAC8HDAC3HDAC4HDAC1
SCHEMBL10845162 0.82 CA12 (0.55) TAAR1HDAC8HDAC3HDAC4HDAC1
SCHEMBL11476379 0.81 NPC1 (0.51) TAAR1HDAC8HDAC3HDAC4HDAC1
SCHEMBL8319084 0.80 TAAR1 (0.43) TBXAS1TAAR1HDAC8HDAC3HDAC4
SCHEMBL7299851 0.79 TAAR1 (0.62) TAAR1LMNACYP2D6KDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0058079-B1 4-(1-IMIDAZOLYLMETHYL)CINNAMIC ACID HYDROCHLORIDE MONOHYDRATE, METHOD OF PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME Kissei Pharmaceutical Co. Ltd. (JP) 1985-01-23 EP claimed
JP-57131769-A None JP disclosed
EP-0294814-B1 Treating agents for renal diseases DAIICHI SEIYAKU CO (JP) 1994-01-12 EP disclosed
EP-0298465-B1 ANTIDIABETIC AGENT DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1993-02-17 EP disclosed
US-4942171-A The compound, 6-(1-imidazolyl methyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid and salts thereof having antidiabetic activity DAIICHI SEIYAKU CO., LTD. (JP) 1990-07-17 US disclosed
EP-0135177-B1 BENZOCYCLOALKANE DERIVATIVES DAIICHI SEIYAKU CO., LTD. (JP) 1989-12-06 EP disclosed
EP-0298465-A2 Antidiabetic agent DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1989-01-11 EP disclosed
EP-0294814-A2 Treating agents for renal diseases DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1988-12-14 EP disclosed
US-4777257-A CARDIOVASCULAR DISORDERS DAIICHI SEIYAKU CO., LTD. (JP) 1988-10-11 US disclosed
US-4665188-A Certain [(1-imidazolyl)-lower-alkylene]-tetrahydronaphthalenecarboxylic acids or corresponding idan-carboxylic acids which are thromboxane A2 DAIICHI SEIYAKU CO., LTD. (JP) 1987-05-12 US disclosed
US-4607046-A THROMBOXANE SYNTHETASE INHIBITOR KISSEI PHARMACEUTICAL CO., LTD. (JP) 1986-08-19 US disclosed
EP-0135177-A2 Benzocycloalkane derivatives DAIICHI SEIYAKU CO., LTD. (JP) 1985-03-27 EP disclosed
EP-0058079-B1 4-(1-IMIDAZOLYLMETHYL)CINNAMIC ACID HYDROCHLORIDE MONOHYDRATE, METHOD OF PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME Kissei Pharmaceutical Co. Ltd. (JP) 1985-01-23 EP disclosed
EP-0058079-A2 4-(1-Imidazolylmethyl)cinnamic acid hydrochloride monohydrate, method of preparation thereof, and pharmaceutical composition containing same Kissei Pharmaceutical Co. Ltd. (JP) 1982-08-18 EP disclosed
JP-S57131769-A 4-(1-IMIDAZOLYLMETHYL)CINNAMIC ACID HYDROCHLORIDE MONOHYDRATE, ITS PREPARATION AND DRUG CONTAINING THE SAME KISSEI PHARMACEUT CO LTD 1982-08-14 JP disclosed
US-4226878-A ANTIINFLAMMATORY, HYPOTENSIVES, ANTIHISTAMINES KISSEI PHARMACEUTICAL CO., LTD. (JP) 1980-10-07 US disclosed