Hydrochloric Acid

Hydrochloric Acid

SCHEMBL218521

Cl.FC(F)(F)c1ccc(CNC2CC2)cc1

nearest known ligand 0.62

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
BCHE known ✓ P06276 2/20 0.62
ACHE known ✓ P22303 2/20 0.62
MAOA known ✓ P21397 1/20 0.53
MAOB known ✓ P27338 1/20 0.53
HRH3 known ✓ Q9Y5N1 1/20 0.50
JAK2 known ✓ O60674 1/20 0.47
JAK1 known ✓ P23458 1/20 0.47
HDAC1 known ✓ Q13547 1/20 0.44
GRIN2B known ✓ Q13224 1/20 0.43
BACE1 P56817 2/20 0.62
TEAD1 P28347 1/20 0.58
MEN1 O00255 1/20 0.56
RAB9A P51151 1/20 0.56
KMT2A Q03164 1/20 0.56
KDM1A O60341 1/20 0.53
POLB P06746 1/20 0.51
TYK2 P29597 1/20 0.47
JAK3 P52333 1/20 0.47
PHGDH O43175 1/20 0.47
ALDH1A1 P00352 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
SCHEMBL5556152 0.98 BCHE (0.64) BCHEACHEBACE1TEAD1MEN1
SCHEMBL24258289 0.91 HRH3 (0.62) BCHEACHEBACE1TEAD1MEN1
SCHEMBL19650799 0.91 BCHE (0.61) BCHEACHEBACE1TEAD1MEN1
SCHEMBL24393407 0.86 BCHE (0.57) BCHEACHEBACE1TEAD1MEN1
SCHEMBL4208525 0.84 ACHE (0.65) BCHEACHEBACE1TEAD1KDM1A
SCHEMBL21729631 0.84 ACHE (0.50) BCHEACHEBACE1TEAD1MEN1
SCHEMBL24258285 0.84 BCHE (0.50) BCHEACHEBACE1TEAD1MEN1
SCHEMBL23545550 0.82 MAOA (0.54) BCHEACHEBACE1TEAD1MEN1
SCHEMBL23545657 0.82 MAOA (0.54) BCHEACHEBACE1TEAD1MEN1
SCHEMBL25253729 0.82 BCHE (0.52) BCHEACHEBACE1TEAD1KDM1A

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2920151-B1 METHOD FOR PRODUCING CARBOXAMIDES BAYER CROPSCIENCE AG (DE) 2017-09-27 EP disclosed
US-9656964-B2 Method for producing carboxamides BAYER CROPSCIENCE AG (DE) 2017-05-23 US disclosed
US-20160009655-A1 METHOD FOR PRODUCING CARBOXAMIDES BAYER CROPSCIENCE AG (DE) 2016-01-14 US disclosed
EP-2920151-A1 METHOD FOR PRODUCING CARBOXAMIDES Bayer Cropscience AG (DE) 2015-09-23 EP disclosed
EP-2351747-B1 Fungicide n-cycloalkyl-benzyl-amide derivatives BAYER IP GMBH (DE) 2014-07-02 EP disclosed
WO-2014076007-A1 METHOD FOR PRODUCING CARBOXAMIDES BAYER CROPSCIENCE AG (DE) 2014-05-22 WO disclosed
EP-1981866-B1 N-cyclopropyl-N-benzylamides as fungicides BAYER CROPSCIENCE AG (DE) 2013-02-27 EP disclosed
CN-101360730-B Fungicide N-cycloalkyl-benzyl-amide derivatives BAYER CROPSCIENCE SA 2012-06-27 CN disclosed
US-8088927-B2 Fungicide N-cycloalkyl-benzyl-amide derivatives BAYER CROPSCIENCE AG (DE) 2012-01-03 US disclosed
EP-2351747-A1 Fungicide n-cycloalkyl-benzyl-amide derivatives Bayer CropScience AG (DE) 2011-08-03 EP disclosed
US-20100286221-A1 Fungicide N-Cycloalkyl-Benzyl-Amide Derivatives BAYER CROPSCIENCE AKTIENGESELLSCHAFT (DE) 2010-11-11 US disclosed
CN-101360730-A Fungicide N-cycloalkyl-benzyl-amide derivatives BAYER CROPSCIENCE SA (FR) 2009-02-04 CN disclosed
EP-1981866-A1 FUNGICIDE N-CYCLOALKYL-BENZYL-AMIDE DERIVATIVES Bayer CropScience S.A. (FR) 2008-10-22 EP disclosed
WO-2007087906-A1 FUNGICIDE N-CYCLOALKYL-BENZYL-AMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2007-08-09 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 (2 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-20160009655-A1 METHOD FOR PRODUCING CARBOXAMIDES CBR3, NQO2, CPS1 BCHE 450/4885ACHE 2576/4885MAOA 1395/4885
US-20100286221-A1 Fungicide N-Cycloalkyl-Benzyl-Amide Derivatives CYP51A1, CBR3, ERG28 BCHE 81/4885ACHE 1038/4885MAOA 677/4885

“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.