Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1648808

Cc1cc(O)c2ccccc2c1N.Cl

nearest known ligand 0.61

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 2/20 0.47
HDAC3 known ✓ O15379 1/20 0.43
HTT P42858 2/20 0.61
LMNA P02545 1/20 0.61
EP300 Q09472 3/20 0.56
MAPT P10636 4/20 0.47
KDM4E B2RXH2 3/20 0.47
HSD17B10 Q99714 2/20 0.47
TP53 P04637 1/20 0.47
PKM P14618 2/20 0.47
IDO1 P14902 2/20 0.43
KAT2B Q92831 2/20 0.43
KAT8 Q9H7Z6 2/20 0.43
NCOR2 Q9Y618 1/20 0.43
TRPM4 Q8TD43 1/20 0.43
ALDH1A1 P00352 2/20 0.42
MEN1 O00255 1/20 0.40
NSD2 O96028 1/20 0.40
POLB P06746 1/20 0.40
KMT2A Q03164 1/20 0.40

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
SCHEMBL353534 0.98 HTT (0.63) HTTLMNAEP300MAPTKDM4E
Hydrochloric Acid SCHEMBL10719596 0.78 PKM (0.61) HTTEP300KDM4EHSD17B10TP53
Hydrochloric Acid SCHEMBL5691548 0.78 PKM (0.61) HTTEP300KDM4EHSD17B10TP53
SCHEMBL866443 0.78 CYP1A2 (0.43) HTTLMNAEP300KDM4EGAA
SCHEMBL1562090 0.78 CYP1A2 (0.50) LMNAEP300KDM4EGAAHSD17B10
SCHEMBL29999289 0.78 CYP1A2 (0.50) LMNAEP300KDM4EGAAHSD17B10
SCHEMBL29462977 0.78 CYP1A2 (0.43) HTTLMNAEP300KDM4EGAA
SCHEMBL352532 0.76 PKM (0.63) HTTLMNAEP300MAPTKDM4E
SCHEMBL29405295 0.76 PKM (0.63) HTTLMNAEP300MAPTKDM4E
Vitamin K3H2 SCHEMBL297164 0.76 HTT (1.00) HTTLMNAEP300MAPTKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20150283290-A1 STERILIZED COMPOSITIONS OF CYANOACRYLATE MONOMERS AND NAPHTHOQUINONE 2,3-OXIDES ADHEZION BIOMEDICAL, LLC (US) 2015-10-08 US claimed
US-4764201-A Plant growth regulation TOMOE KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1988-08-16 US claimed
JP-62190101-A None JP disclosed
JP-62190102-A None JP disclosed
JP-62192302-A None JP disclosed
JP-4046103-A None JP disclosed
US-9717699-B2 Sterilized compositions of cyanoacrylate monomers and naphthoquinone 2,3-oxides ADHEZION BIOMEDICAL, LLC (US) 2017-08-01 US disclosed
US-20160331700-A1 Sterilized Compositions of Cyanoacrylate Monomers and Naphthoquinone 2,3-Oxides H.B. FULLER MEDICAL ADHESIVE TECHNOLOGIES, LLC. 2016-11-17 US disclosed
US-9421297-B2 Sterilized compositions of cyanoacrylate monomers and naphthoquinone 2,3-oxides ADHEZION BIOMEDICAL, LLC (US) 2016-08-23 US disclosed
US-20150283290-A1 STERILIZED COMPOSITIONS OF CYANOACRYLATE MONOMERS AND NAPHTHOQUINONE 2,3-OXIDES ADHEZION BIOMEDICAL, LLC (US) 2015-10-08 US disclosed
EP-2305224-B1 Vitamin K analog for treatment of skin or mucosal ulceration EINSTEIN COLL MED (US) 2015-03-11 EP disclosed
EP-1538136-B1 Fertilizer composition to stimulate the absorption of nutritive substances in plants VALAGRO SPA (IT) 2006-03-08 EP disclosed
WO-2005054156-A1 FERTILIZER COMPOSITION TO STIMULATE THE ABSORPTION OF NUTRITIVE SUBSTANCES IN PLANTS VALAGRO S.P.A. (IT) 2005-06-16 WO disclosed
EP-1538136-A1 Fertilizer composition to stimulate the absorption of nutritive substances in plants Valagro S.p.A. (IT) 2005-06-08 EP disclosed
US-20050119127-A1 Fertilizer composition to stimulate the absorption of nutritive substances in plants VALAGRO S.P.A. (IT) 2005-06-02 US disclosed
JP-H0446103-A GROWTH ACTIVATING AGENT OF CROP FOR AGRICULTURE AND HORTICULTURE AND METHOD FOR REDUCING PHYTOTOXICITY BY HERBICIDE TOMOE KAGAKU KOGYO KK 1992-02-17 JP disclosed
US-4764201-A Plant growth regulation TOMOE KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1988-08-16 US disclosed
JP-S62192302-A STOCK HYPODYNAMIC INHIBITOR FOR STRAWBERRY TOMOE KAGAKU KOGYO KK 1987-08-22 JP disclosed
JP-S62190102-A ADDITIVE FOR SEEDLING RAISING MAT OF PADDY RICE PLANT TOMOE KAGAKU KOGYO KK 1987-08-20 JP disclosed
JP-S62190101-A MATURITY PROMOTER FOR AGRICULTURAL AND HORTICULTURAL CROP TOMOE KAGAKU KOGYO KK 1987-08-20 JP 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 (1 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-20160331700-A1 Sterilized Compositions of Cyanoacrylate Monomers and Naphthoquinone 2,3-Oxides PROC, CCNK, MMS19 GAA 4091/4885HDAC3 3820/4885HTT 4554/4885

“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.