Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1032497

Cl.Cn1cc(C(=O)O)c(C(F)F)n1

nearest known ligand 0.41

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 10)

geneUniProtsupporting neighboursconfidence
KLKB1 known ✓ P03952 1/20 0.33
GAA known ✓ P10253 2/20 0.33
IRAK4 Q9NWZ3 7/20 0.34
ACACB O00763 1/20 0.34
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
CYP11B1 P15538 1/20 0.33
CYP11B2 P19099 1/20 0.33
LMNA P02545 2/20 0.32
POLB P06746 1/20 0.32

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 SCHEMBL8932295 1.00 IRAK4 (0.34) IRAK4ACACBMEN1KMT2ACYP11B1
SCHEMBL20141 0.98 IRAK4 (0.35) IRAK4ACACBMEN1KMT2ACYP11B1
SCHEMBL28726067 0.96 IRAK4 (0.35) IRAK4ACACBMEN1KMT2ACYP11B1
SCHEMBL8932291 0.90 CYP11B1 (0.33) IRAK4ACACBMEN1KMT2ACYP11B1
SCHEMBL31265253 0.86 MEN1 (0.32) ACACBMEN1KMT2AKLKB1
SCHEMBL460661 0.84 LMNA (0.34) GAALMNAPOLB
Hydrochloric Acid SCHEMBL31096988 0.84 ADORA2A (0.36) IRAK4ACACBCYP11B1CYP11B2KLKB1
Hydrochloric Acid SCHEMBL38654637 0.84 KLKB1 (0.34) IRAK4ACACBCYP11B1CYP11B2KLKB1
SCHEMBL14010542 0.84 LMNA (0.35) IRAK4ACACBKMT2ACYP11B1CYP11B2
SCHEMBL345169 0.82 ADORA2A (0.37) IRAK4ACACBCYP11B1CYP11B2KLKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114957123-B 3- (difluoromethyl) -pyrazole-4-carboxylic ester derivative and preparation method and application thereof 浙江工业大学 2023-11-28 CN claimed
CN-119735548-A Improved process for preparing biphenylamide compounds 兰升生物科技集团股份有限公司 2025-04-01 CN disclosed
CN-119431246-A Bispyrimidine marked with dichloro benzene ring carbon-14 and preparation method thereof 浙江爱索拓科技有限公司 2025-02-14 CN disclosed
CN-119285548-A Fluoconazole fungus Process for the preparation of amides 湖南化工研究院有限公司 2025-01-10 CN disclosed
CN-115836041-B Process for producing optically active compound 住友化学株式会社 2024-09-17 CN disclosed
US-20230257408-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2023-08-17 US disclosed
EP-4186882-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2023-05-31 EP disclosed
US-11234439-B2 Imide compound and use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2022-02-01 US disclosed
CN-109661388-B Imide compound and use thereof 住友化学株式会社 2021-11-26 CN disclosed
US-20210274786-A1 IMIDE COMPOUND AND USE THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2021-09-09 US disclosed
US-8273783-B2 Microbiocides SYNGENTA CROP PROTECTION LLC (US) 2012-09-25 US disclosed
US-8268877-B2 Microbiocides SYNGENTA CROP PROTECTION, LLC (US) 2012-09-18 US disclosed
WO-2012113696-A1 NOVEL CARBOXAMIDE MICROBIOCIDES SYNGENTA PARTICIPATIONS AG (CH) 2012-08-30 WO disclosed
EP-2451799-A1 NOVEL MICROBIOCIDES Syngenta Participations AG (CH) 2012-05-16 EP disclosed
US-20120108645-A1 NOVEL MICROBIOCIDES SYNGENTA CROP PROTECTION LLC (US) 2012-05-03 US disclosed
US-20110281924-A1 NOVEL MICROBIOCIDES SYNGENTA CROP PROTECTION LLC (US) 2011-11-17 US disclosed
EP-2379536-A1 NOVEL MICROBIOCIDES Syngenta Participations AG (CH) 2011-10-26 EP disclosed
WO-2011003683-A1 NOVEL MICROBIOCIDES SYNGENTA PARTICIPATIONS AG (CH) 2011-01-13 WO disclosed
WO-2010084078-A1 NOVEL MICROBIOCIDES SYNGENTA PARTICIPATIONS AG (CH) 2010-07-29 WO disclosed
US-5498624-A PLANT FUNGICIDES MONSANTO COMPANY (US) 1996-03-12 US 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 (5 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-20110281924-A1 NOVEL MICROBIOCIDES CD14, FPR1, MPO KLKB1 946/4885GAA 1343/4885IRAK4 1321/4885
US-20230257408-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SIRT1, SIRT3, HCCS KLKB1 4685/4885GAA 2814/4885IRAK4 3536/4885
US-20210274786-A1 IMIDE COMPOUND AND USE THEREOF RAB29, RIN1, RICTOR KLKB1 4867/4885GAA 1115/4885IRAK4 1060/4885
US-20120108645-A1 NOVEL MICROBIOCIDES FPR1, CD14, MPO KLKB1 1126/4885GAA 1489/4885IRAK4 1330/4885
US-11234439-B2 Imide compound and use thereof RAB29, RIN1, RICTOR KLKB1 4867/4885GAA 1115/4885IRAK4 1060/4885

“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.