Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2801770

CNc1ccc(NC)cc1.Cl.Cl

nearest known ligand 0.62

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
CA2 known ✓ P00918 2/20 0.50
ADRA2A known ✓ P08913 2/20 0.48
ADRA2B known ✓ P18089 2/20 0.48
ADRA2C known ✓ P18825 2/20 0.48
KCNH2 known ✓ Q12809 1/20 0.39
GLA known ✓ P06280 1/20 0.35
GAA known ✓ P10253 1/20 0.35
EGFR known ✓ P00533 1/20 0.34
TSHR P16473 1/20 0.62
APP P05067 6/20 0.52
ALDH1A1 P00352 3/20 0.52
MAPT P10636 1/20 0.52
RECQL P46063 2/20 0.50
HSD17B10 Q99714 2/20 0.50
CA12 O43570 2/20 0.50
CA1 P00915 1/20 0.50
TP53 P04637 1/20 0.50
CYP3A4 P08684 1/20 0.50
THRB P10828 1/20 0.50
HPGD P15428 1/20 0.50

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 SCHEMBL6241253 1.00 TSHR (0.62) TSHRAPPALDH1A1MAPTRECQL
SCHEMBL153943 0.96 TSHR (0.67) TSHRAPPALDH1A1MAPTRECQL
Bromide SCHEMBL7630752 0.92 TSHR (0.62) TSHRAPPALDH1A1MAPTRECQL
Hydrochloric Acid SCHEMBL9647124 0.88 TSHR (0.59) TSHRAPPALDH1A1MAPTRECQL
Hydrochloric Acid SCHEMBL2866389 0.87 MAPT (0.50) TSHRAPPALDH1A1MAPTRECQL
SCHEMBL7338618 0.85 TSHR (0.56) TSHRAPPALDH1A1MAPTRECQL
SCHEMBL5147226 0.85 KIF11 (0.64) TSHRAPPALDH1A1MAPTRECQL
Hydrochloric Acid SCHEMBL8724196 0.84 ALDH1A1 (0.73) TSHRAPPALDH1A1MAPTRECQL
Hydrochloric Acid SCHEMBL6010014 0.84 TSHR (0.48) TSHRAPPALDH1A1MAPTRECQL
Hydrochloric Acid SCHEMBL10343601 0.84 ALDH1A1 (0.48) TSHRAPPALDH1A1MAPTRECQL

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-11834697-B2 Electrochemical recognition and quantification of cytochrome c oxidase expression in bacteria OXFORD UNIVERSITY INNOVATION LIMITED (GB) 2023-12-05 US disclosed
CN-116940828-A Method for determining total aldehydes in one or more of crude 2, 5-furandicarboxylic acid (FDCA), crude terephthalic acid (TPA), and esters thereof 阿彻丹尼尔斯米德兰德公司 2023-10-24 CN disclosed
US-20200199644-A1 ELECTROCHEMICAL RECOGNITION AND QUANTIFICATION OF CYTOCHROME C OXIDASE EXPRESSION IN BACTERIA OXFORD UNIVERSITY INNOVATION LIMITED (GB) 2020-06-25 US disclosed
US-8530191-B2 Method for preventing formation of trisulfide derivatives of polypeptides NOVO NORDISK A/S (DK) 2013-09-10 US disclosed
US-20100160236-A1 Method for Preventing Formation of Trisulfide Derivatives of Polypeptides NOVO NORDISK HEALTHCARE A/G (CH) 2010-06-24 US disclosed
EP-1833841-B1 METHOD FOR PREVENTING FORMATION OF TRISULFIDE DERIVATIVES OF POLYPEPTIDES NOVO NORDISK HEALTHCARE AG (CH) 2010-04-07 EP disclosed
US-20090131311-A1 Method for Preventing Formation of Trisulfide Derivatives of Polypeptides NOVO NORDISK HEALTHCARE AG 2009-05-21 US disclosed
US-4009154-A Process for preparing aromatic polyamides with sodium carbonate hydrate as acid acceptor TEIJIN LIMITED (JA) 1977-02-22 US disclosed