Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6767821

Cl.O=C(O)Cc1ccccc1CC(=O)O

nearest known ligand 0.73

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
PTGS1 known ✓ P23219 2/20 0.50
GAA known ✓ P10253 1/20 0.50
PTGS2 known ✓ P35354 2/20 0.48
TTR known ✓ P02766 1/20 0.48
ADRA1A known ✓ P35348 1/20 0.48
MMP1 known ✓ P03956 1/20 0.48
MMP8 known ✓ P22894 1/20 0.48
MMP13 known ✓ P45452 1/20 0.48
GRIN2D known ✓ O15399 1/20 0.47
GRIN3B known ✓ O60391 1/20 0.47
GRIN1 known ✓ Q05586 1/20 0.47
GRIN2A known ✓ Q12879 1/20 0.47
GRIN2B known ✓ Q13224 1/20 0.47
GRIN2C known ✓ Q14957 1/20 0.47
GRIN3A known ✓ Q8TCU5 1/20 0.47
AKR1B1 P15121 2/20 0.73
TDP1 Q9NUW8 1/20 0.61
BCAT2 O15382 1/20 0.53
KDM4E B2RXH2 1/20 0.52
CYP1A2 P05177 1/20 0.52

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 SCHEMBL9621764 1.00 AKR1B1 (0.73) AKR1B1TDP1BCAT2KDM4ECYP1A2
SCHEMBL30359 0.97 AKR1B1 (0.76) AKR1B1TDP1BCAT2KDM4ECYP1A2
SCHEMBL29410826 0.97 AKR1B1 (0.76) AKR1B1TDP1BCAT2KDM4ECYP1A2
Hydrogen Sulfide SCHEMBL27426416 0.94 AKR1B1 (0.73) AKR1B1TDP1BCAT2KDM4ECYP1A2
Iodide SCHEMBL31305035 0.94 AKR1B1 (0.73) AKR1B1TDP1BCAT2KDM4ECYP1A2
SCHEMBL28842838 0.94 AKR1B1 (0.73) AKR1B1TDP1BCAT2KDM4ECYP1A2
Methyl Alcohol SCHEMBL28299530 0.92 AKR1B1 (0.70) AKR1B1TDP1BCAT2KDM4ECYP1A2
Hydrochloric Acid SCHEMBL8100842 0.91 AKR1B1 (0.61) AKR1B1TDP1BCAT2KDM4ECYP1A2
SCHEMBL8851626 0.91 AKR1B1 (0.61) AKR1B1TDP1BCAT2KDM4ECYP1A2
Ethylene Glycol SCHEMBL28068140 0.90 AKR1B1 (0.67) AKR1B1TDP1BCAT2KDM4ECYP1A2

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
US-20040068062-A1 Hydroxyaliphatic functional epoxy resins WALKER LOUIS L (US) 2004-04-08 US disclosed
US-6613849-B2 Curable multifunctional glycidyl ethers and acrylated derivatives thereof, for example the diglycidyl ether of 1,2-bis(4-hydroxyphenyl)-2-hydroxypropane; thermosetting resins; higher reactivity during curing THE DOW CHEMICAL COMPANY 2003-09-02 US disclosed
US-20020091223-A1 Hydroxyaliphatic functional epoxy resins WALKER LOUIS L (US) 2002-07-11 US disclosed
US-6353079-B1 DIGLYCIDYL ETHER OF BISPHENOL CONTAINING HYDROXYALIPHATIC GROUP LINKAGE BETWEEN TWO AROMATIC RINGS OF BISPHENOL THE DOW CHEMICAL COMPANY 2002-03-05 US disclosed
US-3935239-A Process for producing aromatic α-diketones NEILAND OYAR YANOVICH 1976-01-27 US disclosed