Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7206595

Cl.Cn1cnc2ccccc21

nearest known ligand 0.57

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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
TDP1 Q9NUW8 1/20 0.57
GRM5 P41594 1/20 0.51
HTT P42858 4/20 0.50
CYP11B1 P15538 4/20 0.49
CYP11B2 P19099 4/20 0.49
LMNA P02545 3/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
MEN1 O00255 1/20 0.47
HPGD P15428 1/20 0.47
KMT2A Q03164 1/20 0.47
HSD17B10 Q99714 1/20 0.47
PKM P14618 1/20 0.46
POLB P06746 1/20 0.46
TNF P01375 1/20 0.46
EGLN3 Q9H6Z9 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44

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 SCHEMBL3713895 1.00 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL5399 0.98 TDP1 (0.59) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL29359161 0.98 TDP1 (0.59) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL28652434 0.95 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Bromide SCHEMBL10432264 0.95 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Iodide SCHEMBL15375366 0.95 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Bromide SCHEMBL6955674 0.95 TDP1 (0.57) TDP1GRM5HTTCYP11B1CYP11B2
Methylamine SCHEMBL28557648 0.93 TDP1 (0.55) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL30395666 0.90 TDP1 (0.52) TDP1GRM5HTTCYP11B1CYP11B2
SCHEMBL15639423 0.90 TDP1 (0.52) TDP1GRM5HTTCYP11B1CYP11B2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115155655-B Nonmetal liquid phase catalyst, application thereof and method for synthesizing chloroethylene 厦门中科易工化学科技有限公司 2024-08-06 CN claimed
CN-115155655-A Nonmetal liquid phase catalyst, application thereof and method for synthesizing chloroethylene 厦门中科易工化学科技有限公司 2022-10-11 CN claimed
EP-3166981-B1 OLIGOSACCHARIDE COMPOSITIONS AND METHODS FOR PRODUCING THEREOF DSM NUTRITIONAL PRODUCTS LLC (US) 2026-05-13 EP disclosed
CN-119100907-A Synthetic method of chloroethylene and polyvinyl chloride 厦门中科易工化学科技有限公司 2024-12-10 CN disclosed
EP-3459975-B1 POLYMERIC ACID CATALYSTS AND USES THEREOF DSM NUTRITIONAL PRODUCTS LLC (US) 2024-10-02 EP disclosed
CN-115155655-B Nonmetal liquid phase catalyst, application thereof and method for synthesizing chloroethylene 厦门中科易工化学科技有限公司 2024-08-06 CN disclosed
US-11584805-B2 Oligosaccharide compositions and methods for producing thereof DSM NUTRITIONAL PRODUCTS, LLC (US) 2023-02-21 US disclosed
CN-115155655-A Nonmetal liquid phase catalyst, application thereof and method for synthesizing chloroethylene 厦门中科易工化学科技有限公司 2022-10-11 CN disclosed
US-11059791-B2 Non-coordinating anion type benzimidazolium activators EXXONMOBIL CHEMICAL PATENTS INC. (US) 2021-07-13 US disclosed
US-20210002387-A1 OLIGOSACCHARIDE COMPOSITIONS AND METHODS FOR PRODUCING THEREOF HERCULES CAPITAL, INC. 2021-01-07 US disclosed
US-20200339517-A1 Non-Coordinating Anion Type Benzimidazolium Activators EXXONMOBIL CHEMICAL PATENTS INC. 2020-10-29 US disclosed
WO-2013163230-A2 BIO-BASED POLYMERS AND METHODS OF PRODUCING THEREOF Midori Renewables, Inc. (US) 2013-10-31 WO disclosed
US-20130233308-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF Midori Renewables, Inc. (US) 2013-09-12 US disclosed
US-8476388-B2 Polymeric acid catalysts and uses thereof Midori Renewables, Inc. (US) 2013-07-02 US disclosed
US-8466242-B2 Polymeric acid catalysts and uses thereof Midori Renewables, Inc. (US) 2013-06-18 US disclosed
US-20130042859-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF Midori Renewables, Inc. (US) 2013-02-21 US disclosed
US-20120252957-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF Midori Renewables, Inc. (US) 2012-10-04 US disclosed
WO-2012118767-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF Midori Renewables, Inc. (US) 2012-09-07 WO disclosed
US-20120220740-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF Midori Renewables, Inc. (US) 2012-08-30 US disclosed
WO-2003016612-A1 TEXTILE TREATMENT SANYO CHEMICAL INDUSTRIES, LTD. (JP) 2003-02-27 WO 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 (6 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-20210002387-A1 OLIGOSACCHARIDE COMPOSITIONS AND METHODS FOR PRODUCING THEREOF OSTC, FUT5, FUT6 TDP1 4531/4885GRM5 3677/4885HTT 4163/4885
US-11584805-B2 Oligosaccharide compositions and methods for producing thereof OSTC, FUT5, FUT6 TDP1 4531/4885GRM5 3677/4885HTT 4163/4885
US-20120252957-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF MGAM, PGLS, GAA TDP1 1313/4885GRM5 3835/4885HTT 3885/4885
US-20120220740-A1 POLYMERIC ACID CATALYSTS AND USES THEREOF MGAM, PGLS, GAA TDP1 1343/4885GRM5 3811/4885HTT 3784/4885
US-20200339517-A1 Non-Coordinating Anion Type Benzimidazolium Activators VDAC1, MYB, BID TDP1 2981/4885GRM5 4614/4885HTT 828/4885
US-11059791-B2 Non-coordinating anion type benzimidazolium activators VDAC1, MYB, BID TDP1 2981/4885GRM5 4614/4885HTT 828/4885

“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.