Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2212596

Cl.Cl.O=c1c(O)c(O)c1=O.O=c1c(O)c(O)c1=O

nearest known ligand 0.36

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 16)

geneUniProtsupporting neighboursconfidence
GSTP1 known ✓ P09211 1/20 0.36
GSR P00390 1/20 0.36
TXNRD1 Q16881 1/20 0.36
TXNRD3 Q86VQ6 1/20 0.36
TXNRD2 Q9NNW7 1/20 0.36
KDM4E B2RXH2 2/20 0.36
ALDH1A1 P00352 2/20 0.36
TDP1 Q9NUW8 2/20 0.36
MEN1 O00255 1/20 0.36
MAPT P10636 1/20 0.36
ALOX15 P16050 1/20 0.36
ALOX12 P18054 1/20 0.36
BLM P54132 1/20 0.36
KMT2A Q03164 1/20 0.36
LMNA P02545 1/20 0.33
HSD17B10 Q99714 1/20 0.33

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
SCHEMBL56172 0.95
Ammonia Solution, Strong SCHEMBL7105974 0.90 GSR (0.36) GSRGSTP1TXNRD1TXNRD3TXNRD2
SCHEMBL916303 0.90 GSR (0.36) GSRGSTP1TXNRD1TXNRD3TXNRD2
Fluoride SCHEMBL915482 0.90
Methane SCHEMBL88300 0.90
Water SCHEMBL8171778 0.90
SCHEMBL14716520 0.86 KDM4E (0.43) GSRGSTP1TXNRD1TXNRD3TXNRD2
Water SCHEMBL4930788 0.86 KDM4E (0.40) GSRGSTP1TXNRD1TXNRD3TXNRD2
Water SCHEMBL9057534 0.86 KDM4E (0.40) GSRGSTP1TXNRD1TXNRD3TXNRD2
Water SCHEMBL19019782 0.86 KDM4E (0.40) GSRGSTP1TXNRD1TXNRD3TXNRD2

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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230279244-A1 RESIN COMPOSITION, COATED AND DRIED PRODUCT, MELT-KNEADED PRODUCT, OPTICAL FILTER, IMAGE DISPLAY DEVICE, SOLID-STATE IMAGING ELEMENT, SQUARYLIUM COMPOUND, AND METHOD FOR PRODUCING THE SAME FUJIFILM CORPORATION (JP) 2023-09-07 US disclosed
US-11342504-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use NOVALED GMBH (DE) 2022-05-24 US disclosed
US-20200152873-A1 Oxocarbon-, Pseudooxocarbon- and Radialene Compounds and Their Use NOVALED GMBH (DE) 2020-05-14 US disclosed
US-10586926-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use NOVALED GMBH (DE) 2020-03-10 US disclosed
EP-3319940-B1 NEW INDOLE COMPOUNDS HAVING ANTIPROTOZOAL ACTIVITY AND ITS USE AS WELL AS METHODS FOR PRODUCING THE SAME UNIV BRAUNSCHWEIG TECH (DE) 2019-05-29 EP disclosed
US-10287271-B2 Indole compounds having antiprotozoal activity and its use as well as methods for producing the same TECHNISCHE UNIVERSITAET BRAUNSCHWEIG (DE) 2019-05-14 US disclosed
US-20180194750-A1 NEW INDOLE COMPOUNDS HAVING ANTIPROTOZOAL ACTIVITY AND ITS USE AS WELL AS METHODS FOR PRODUCING THE SAME TECHNISCHE UNIVERSITAET BRAUNSCHWEIG (DE) 2018-07-12 US disclosed
EP-3319940-A1 NEW INDOLE COMPOUNDS HAVING ANTIPROTOZOAL ACTIVITY AND ITS USE AS WELL AS METHODS FOR PRODUCING THE SAME Technische Universität Braunschweig (DE) 2018-05-16 EP disclosed
US-20180076389-A1 Oxocarbon-, Pseudooxocarbon- and Radialene Compounds and Their Use NOVALED GMBH (DE) 2018-03-15 US disclosed
US-9876172-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use NOVALED GMBH (DE) 2018-01-23 US disclosed
US-8617426-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use NOVALED AG (DE) 2013-12-31 US disclosed
US-20110309309-A1 Oxocarbon-, Pseudooxocarbon- and Radialene Compounds and Their Use NOVALED AG (DE) 2011-12-22 US disclosed
US-7981324-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use NOVALED AG (DE) 2011-07-19 US disclosed
US-20100266507-A1 LUMINESCENT COMPOUNDS SETA BIOMEDICALS, LLC 2010-10-21 US disclosed
US-20080265216-A1 Use as doping agent for doping organic semiconductive matrix material, as blocker material, as charge injection layer, as electrode material as well as organic semiconductor, electronic component; 1,3-Bi(dicyanomethylene)indane-2-ylidene-bis(4-oxo-[3,5-di-t-butyl]-2,5-cyclohexadienylidene)cyclopropane NOVALED AG (DE) 2008-10-30 US disclosed
US-7242542-B2 Filters of electronic displays KYOWA HAKKO CHEMICAL CO., LTD. (JP) 2007-07-10 US disclosed
CN-1320378-C Filter for electronic display device KYOWA HAKKO CHEMICAL CO LTD (JP) 2007-06-06 CN disclosed
US-20060063864-A1 Filters of electronic displays KYOWA HAKKO CHEMICAL CO., LTD (JP) 2006-03-23 US disclosed
CN-1659456-A Filter for electronic display device KYOWA HAKKO CHEMICAL CO LTD (JP) 2005-08-24 CN disclosed
EP-1521107-A1 FILTERS FOR ELECTRONIC DISPLAYS Kyowa Hakko Chemical Co., Ltd. (JP) 2005-04-06 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (10 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100266507-A1 LUMINESCENT COMPOUNDS SQLE, COASY, ZKSCAN2 GSTP1 1960/4885GSR 356/4885TXNRD1 1263/4885
US-20180076389-A1 Oxocarbon-, Pseudooxocarbon- and Radialene Compounds and Their Use DNMT3B, CHRNB1, CHRNB2 GSTP1 4639/4885GSR 4686/4885TXNRD1 4452/4885
US-20180194750-A1 NEW INDOLE COMPOUNDS HAVING ANTIPROTOZOAL ACTIVITY AND ITS USE AS WELL AS METHODS FOR PRODUCING THE SAME IDO1, IDO2, INMT GSTP1 849/4885GSR 347/4885TXNRD1 1717/4885
US-20200152873-A1 Oxocarbon-, Pseudooxocarbon- and Radialene Compounds and Their Use DNMT3B, CHRNB1, CHRNB2 GSTP1 4639/4885GSR 4686/4885TXNRD1 4452/4885
US-10586926-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use DNMT3B, CHRNB1, CHRNB2 GSTP1 4639/4885GSR 4686/4885TXNRD1 4452/4885
US-10287271-B2 Indole compounds having antiprotozoal activity and its use as well as methods for producing the same IDO1, IDO2, INMT GSTP1 788/4885GSR 474/4885TXNRD1 1924/4885
US-20230279244-A1 RESIN COMPOSITION, COATED AND DRIED PRODUCT, MELT-KNEADED PRODUCT, OPTICAL FILTER, IMAGE DISPLAY DEVICE, SOLID-STATE IMAGING ELEMENT, SQUARYLIUM COMPOUND, AND METHOD FOR PRODUCING THE SAME KLK5, KLHDC2, TNFRSF9 GSTP1 4165/4885GSR 4615/4885TXNRD1 3826/4885
US-11342504-B2 Oxocarbon-, pseudooxocarbon- and radialene compounds and their use DNMT3B, CHRNB1, CHRNB2 GSTP1 4639/4885GSR 4686/4885TXNRD1 4452/4885
US-20110309309-A1 Oxocarbon-, Pseudooxocarbon- and Radialene Compounds and Their Use DNMT3B, CHRNB1, CHRNB2 GSTP1 4639/4885GSR 4686/4885TXNRD1 4452/4885
US-20080265216-A1 Use as doping agent for doping organic semiconductive matrix material, as blocker material, as charge injection layer, as electrode material as well as organic semiconductor, electronic component; 1,3-Bi(dicyanomethylene)indane-2-ylidene-bis(4-oxo-[3,5-di-t-butyl]-2,5-cyclohexadienylidene)cyclopropane CHRNB1, GJB2, CHRNB3 GSTP1 4484/4885GSR 4561/4885TXNRD1 4767/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.