Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9014930

Cc1c(O)c(N)cc(N)c1O.Cl.Cl

nearest known ligand 0.50

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
GAA known ✓ P10253 3/20 0.50
PIK3CA known ✓ P42336 1/20 0.35
ACHE known ✓ P22303 1/20 0.35
CA2 known ✓ P00918 1/20 0.35
HSP90AA1 known ✓ P07900 1/20 0.34
HSP90AB1 known ✓ P08238 1/20 0.34
ALDH1A1 P00352 5/20 0.50
MAPT P10636 3/20 0.50
KDM4E B2RXH2 3/20 0.50
LMNA P02545 1/20 0.50
PTK2 Q05397 1/20 0.39
ALOX15 P16050 3/20 0.39
HSD17B10 Q99714 2/20 0.39
PKM P14618 1/20 0.38
CYP3A4 P08684 4/20 0.35
TSHR P16473 3/20 0.35
SELL P14151 1/20 0.35
SELP P16109 1/20 0.35
SELE P16581 1/20 0.35
MAPK1 P28482 1/20 0.35

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 SCHEMBL27979336 1.00 ALDH1A1 (0.50) ALDH1A1GAAMAPTKDM4ELMNA
SCHEMBL5028438 0.97 ALDH1A1 (0.52) ALDH1A1GAAMAPTKDM4ELMNA
Benzene SCHEMBL28239798 0.92 ALDH1A1 (0.48) ALDH1A1GAAMAPTKDM4ELMNA
SCHEMBL28575233 0.86 ALDH1A1 (0.48) ALDH1A1GAAMAPTKDM4ELMNA
SCHEMBL19730667 0.83 ALDH1A1 (0.46) ALDH1A1GAAMAPTKDM4ELMNA
Cystamine SCHEMBL28068510 0.81 MAPT (0.42) ALDH1A1GAAMAPTKDM4ELMNA
SCHEMBL9500782 0.79 TRPA1 (0.46) ALDH1A1GAAMAPTKDM4ELMNA
SCHEMBL3618414 0.78 ALDH1A1 (0.46) ALDH1A1GAAMAPTKDM4ELMNA
SCHEMBL12127221 0.78 ALDH1A1 (0.52) ALDH1A1GAAMAPTKDM4ELMNA
Hydrochloric Acid SCHEMBL5162607 0.78 PTK2 (0.47) ALDH1A1GAAMAPTKDM4ELMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107417918-B Cross-linkable PBO copolymer and preparation method and application thereof 郑州大学 2022-03-01 CN claimed
CN-105504270-B The preparation method of crosslinked polyphenylene Benzo-dioxazole film 郑州大学 2018-06-08 CN claimed
CN-106810696-A Cross-linking poly- alkylene Benzo-dioxazole and preparation method thereof 郑州大学 2017-06-09 CN claimed
CN-103980133-B A kind of method preparing 2-methyl-4,6-diaminoresorcinol dihydrochloride 郑州大学 2016-06-08 CN claimed
CN-105504270-A Preparation method of crosslinking poly(p-phenylenebenzobisoxazole) film UNIV ZHENGZHOU 2016-04-20 CN claimed
CN-103980133-A Method for preparing 2-methyl-4,6-diaminoresorcinol hydrochloride UNIV ZHENGZHOU 2014-08-13 CN claimed
CN-107417918-B Cross-linkable PBO copolymer and preparation method and application thereof 郑州大学 2022-03-01 CN disclosed
CN-107417918-B Cross-linkable PBO copolymer and preparation method and application thereof 郑州大学 2022-03-01 CN disclosed
CN-105504270-B The preparation method of crosslinked polyphenylene Benzo-dioxazole film 郑州大学 2018-06-08 CN disclosed
CN-107417918-A Cross-linking PBO copolymers and its production and use 郑州大学 2017-12-01 CN disclosed
CN-106810696-A Cross-linking poly- alkylene Benzo-dioxazole and preparation method thereof 郑州大学 2017-06-09 CN disclosed
CN-103980133-B A kind of method preparing 2-methyl-4,6-diaminoresorcinol dihydrochloride 郑州大学 2016-06-08 CN disclosed
CN-103980133-B A kind of method preparing 2-methyl-4,6-diaminoresorcinol dihydrochloride 郑州大学 2016-06-08 CN disclosed
US-5021580-A Monomer containing aromatic group, two amine, two hydroxy, and a methyl groups THE DOW CHEMICAL COMPANY (US) 1991-06-04 US disclosed
US-4982001-A Process for the preparation of amino-1,3-benzenediol THE DOW CHEMICAL COMPANY (US) 1991-01-01 US disclosed
EP-0392008-A1 COPOLYMERS CONTAINING POLYBENZOXAZOLE, POLYBENZOTHIAZOLE AND POLYBENZIMIDAZOLE MOIETIES THE DOW CHEMICAL COMPANY (US) 1990-10-17 EP disclosed
EP-0368006-A2 Copolymers containing polybenzoxazole polybenzothiazole and polybenzimidazole moieties THE DOW CHEMICAL COMPANY (US) 1990-05-16 EP disclosed
WO-1990003995-A1 COPOLYMERS CONTAINING POLYBENZOXAZOLE, POLYBENZOTHIAZOLE AND POLYBENZIMIDAZOLE MOIETIES THE DOW CHEMICAL COMPANY (US) 1990-04-19 WO disclosed
US-4912246-A 1,3-bis(alkylcarbonato)-nitrobenzenes THE DOW CHEMICAL COMPANY (US) 1990-03-27 US disclosed
EP-0312931-A2 Process for the preparation of amino-1,3 benzenediol THE DOW CHEMICAL COMPANY (US) 1989-04-26 EP disclosed