Hydrochloric Acid

Hydrochloric Acid

SCHEMBL28625633

CCCC(=O)Oc1cscc1N.Cl

nearest known ligand 0.41

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 0.33
GAA known ✓ P10253 4/20 0.31
GLA known ✓ P06280 1/20 0.31
HTR1A known ✓ P08908 1/20 0.31
DRD2 known ✓ P14416 1/20 0.31
DRD1 known ✓ P21728 1/20 0.31
HTR2A known ✓ P28223 1/20 0.31
ALOX15 P16050 2/20 0.41
ALDH1A1 P00352 4/20 0.36
BCL9 O00512 1/20 0.36
CTNNB1 P35222 1/20 0.36
LMNA P02545 1/20 0.36
KMT2A Q03164 5/20 0.36
KDM4E B2RXH2 3/20 0.36
MEN1 O00255 3/20 0.36
RECQL P46063 1/20 0.36
RAB9A P51151 2/20 0.32
MAPT P10636 4/20 0.31
POLM Q9NP87 1/20 0.31
POLK Q9UBT6 1/20 0.31

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
SCHEMBL28625769 0.98 ALOX15 (0.42) ALOX15ALDH1A1BCL9CTNNB1LMNA
Hydrochloric Acid SCHEMBL29011989 0.90 KMT2A (0.47) ALOX15LMNAKMT2AKDM4EMEN1
Hydrochloric Acid SCHEMBL29012008 0.86 HIF1A (0.41) ALOX15ALDH1A1LMNAKMT2AKDM4E
SCHEMBL6586460 0.75 ALDH1A1 (0.40) ALOX15ALDH1A1LMNAKMT2AKDM4E
Hydrochloric Acid SCHEMBL28629504 0.74 ALDH1A1 (0.39) ALDH1A1LMNAKMT2AKDM4EMEN1
SCHEMBL13719980 0.73 ALDH1A1 (0.51) ALOX15ALDH1A1BCL9CTNNB1LMNA
SCHEMBL1162157 0.72 KDM4E (0.51) ALOX15ALDH1A1BCL9CTNNB1LMNA
SCHEMBL2744773 0.72 LMNA (0.50) ALOX15ALDH1A1LMNAKMT2AKDM4E
SCHEMBL2744922 0.72 LMNA (0.50) ALOX15ALDH1A1LMNAKMT2AKDM4E
SCHEMBL28834444 0.71 KDM4E (0.46) ALOX15ALDH1A1BCL9CTNNB1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113387959-B Synthesis method of thieno [3,2-c ] pyridine-6-carboxylic acid methyl ester 烟台理工学院 2023-05-05 CN claimed
CN-113387959-A Synthetic method of thieno [3,2-c ] pyridine-6-carboxylic acid methyl ester 烟台理工学院 2021-09-14 CN claimed
CN-113387959-B Synthesis method of thieno [3,2-c ] pyridine-6-carboxylic acid methyl ester 烟台理工学院 2023-05-05 CN disclosed
CN-113387959-A Synthetic method of thieno [3,2-c ] pyridine-6-carboxylic acid methyl ester 烟台理工学院 2021-09-14 CN disclosed
CN-113387959-A Synthetic method of thieno [3,2-c ] pyridine-6-carboxylic acid methyl ester 烟台理工学院 2021-09-14 CN disclosed