Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5197296

Cl.O=C1C=CC(=O)C(O)=C1

nearest known ligand 0.43

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
MAOA known ✓ P21397 4/20 0.39
MAOB known ✓ P27338 4/20 0.39
ACHE known ✓ P22303 2/20 0.39
BCHE known ✓ P06276 1/20 0.39
ERBB2 known ✓ P04626 2/20 0.39
GLA known ✓ P06280 1/20 0.36
TOP1 known ✓ P11387 1/20 0.30
MAPT P10636 7/20 0.43
ALDH1A1 P00352 6/20 0.43
HPGD P15428 6/20 0.43
TDP1 Q9NUW8 5/20 0.43
MEN1 O00255 5/20 0.43
KMT2A Q03164 5/20 0.43
RECQL P46063 3/20 0.43
ALOX12 P18054 2/20 0.43
MAPK1 P28482 5/20 0.39
BLM P54132 3/20 0.39
HSD17B10 Q99714 3/20 0.39
APEX1 P27695 2/20 0.39
CASP1 P29466 2/20 0.39

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
SCHEMBL28134388 0.97 MAPT (0.46) MAPTALDH1A1HPGDTDP1MEN1
SCHEMBL221723 0.97
SCHEMBL28131185 0.94 MAPT (0.43) MAPTALDH1A1HPGDTDP1MEN1
SCHEMBL27825791 0.94 MAPT (0.43) MAPTALDH1A1HPGDTDP1MEN1
SCHEMBL28096606 0.94
Methoxymethane SCHEMBL790782 0.87 ERBB2 (0.50) MAPTALDH1A1HPGDTDP1MEN1
Trimethylammonium SCHEMBL27729208 0.87 ERBB2 (0.39) MAPTALDH1A1HPGDTDP1MEN1
Ethylenediamine SCHEMBL9133919 0.85 ALDH1A1 (0.37) MAPTALDH1A1HPGDTDP1MEN1
Phenol SCHEMBL28096443 0.81 TDP1 (0.48) MAPTALDH1A1HPGDTDP1MEN1
Pyrogallol SCHEMBL10768188 0.79 RECQL (0.50) MAPTALDH1A1HPGDTDP1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8642089-B2 Melt extrusion of salts of active ingredients EVONIK ROEHM GMBH (DE) 2014-02-04 US claimed
EP-1478344-B1 MELT EXTRUSION CONSISTING OF SALTS OF ACTIVE INGREDIENTS ROEHM GMBH (DE) 2007-05-23 EP claimed
US-20040253314-A1 Melt extrusion of salts of active ingredients ROEHM GMBH (DE) 2004-12-16 US claimed
CN-106282135-B It the preparation method of quinine ketoreductase RrQR a kind of and its is applied in preparation (R) -3- quinuclidinol 河北省科学院生物研究所 2019-09-27 CN disclosed
US-8642089-B2 Melt extrusion of salts of active ingredients EVONIK ROEHM GMBH (DE) 2014-02-04 US disclosed
US-20040253314-A1 Melt extrusion of salts of active ingredients ROEHM GMBH (DE) 2004-12-16 US disclosed
CN-1205020-A Polyphenylene sulfide resin composition TORAY INDUSTRIES (JP) 1999-01-13 CN disclosed