Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8675457

Cl.O=C(O)c1cccc2c1C(=O)c1ccccc1C2=O

nearest known ligand 0.96

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
TTR known ✓ P02766 1/20 0.60
ALDH1A1 P00352 4/20 0.96
L3MBTL1 Q9Y468 1/20 0.96
MAPT P10636 8/20 0.82
LMNA P02545 2/20 0.82
MEN1 O00255 4/20 0.62
KMT2A Q03164 4/20 0.62
MAPK1 P28482 4/20 0.62
POLB P06746 2/20 0.62
THRB P10828 2/20 0.62
RECQL P46063 1/20 0.62
KEAP1 Q14145 2/20 0.58
NFE2L2 Q16236 1/20 0.58
KDM4E B2RXH2 3/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
MMP14 P50281 1/20 0.57
CYP1A2 P05177 1/20 0.55
CYP2D6 P10635 1/20 0.55
CYP2C9 P11712 1/20 0.55
TSHR P16473 1/20 0.55

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
SCHEMBL461660 0.98 ALDH1A1 (1.00) ALDH1A1L3MBTL1MAPTLMNAMEN1
Anthraquinone SCHEMBL8941397 0.98 ALDH1A1 (1.00) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL69132 0.92 ALDH1A1 (0.88) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL31276140 0.90 ALDH1A1 (0.85) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL30808237 0.90 ALDH1A1 (0.85) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL581124 0.90 ALDH1A1 (1.00) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL600330 0.90 ALDH1A1 (0.85) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL69960 0.90 ALDH1A1 (0.85) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL27456684 0.87 ALDH1A1 (0.78) ALDH1A1L3MBTL1MAPTLMNAMEN1
SCHEMBL27360880 0.84 ALDH1A1 (0.75) ALDH1A1L3MBTL1MAPTLMNAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5785943-A HYDROGENATION OF SUPPORTED ANTHRAQUINONE TO ANTHRAHYDROQUINONE FOLLOWED BY REACTION WITH OXYGEN; SOLVENT EXTRACTION GUILLET JAMES E (CA) 1998-07-28 US claimed
EP-0673348-A1 PRODUCTION OF HYDROGEN PEROXIDE GUILLET, James Edwin (CA) 1995-09-27 EP claimed
WO-1995010480-A1 PRODUCTION OF HYDROGEN PEROXIDE GUILLET JAMES E (CA) 1995-04-20 WO claimed
EP-3543209-A1 PROCESS FOR MANUFACTURING AN AQUEOUS HYDROGEN PEROXIDE SOLUTION SOLVAY SA (BE) 2019-09-25 EP disclosed
US-5785943-A HYDROGENATION OF SUPPORTED ANTHRAQUINONE TO ANTHRAHYDROQUINONE FOLLOWED BY REACTION WITH OXYGEN; SOLVENT EXTRACTION GUILLET JAMES E (CA) 1998-07-28 US disclosed
EP-0673348-A1 PRODUCTION OF HYDROGEN PEROXIDE GUILLET, James Edwin (CA) 1995-09-27 EP disclosed
WO-1995010480-A1 PRODUCTION OF HYDROGEN PEROXIDE GUILLET JAMES E (CA) 1995-04-20 WO disclosed
US-4329456-A ACYLATION WITHOUT INTERMEDIATE ISOLATION CIBA-GEIGY AG (CH) 1982-05-11 US disclosed
US-4265633-A Process for the manufacture of vat dyes CIBA-GEIGY AG (CH) 1981-05-05 US disclosed