Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2379468

Cl.O=C(O)c1ccc(-c2cnc3ncc(Cc4ccc5ncccc5c4)n3n2)cc1F

nearest known ligand 0.82

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 3)

geneUniProtsupporting neighboursconfidence
MET known ✓ P08581 20/20 0.82
KCNH2 known ✓ Q12809 1/20 0.54
CDKL5 O76039 1/20 0.82

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 SCHEMBL1427191 1.00 MET (0.82) METCDKL5KCNH2
SCHEMBL1427684 0.99 MET (0.84) METCDKL5KCNH2
Capmatinib SCHEMBL3843257 0.93 MET (0.95) METCDKL5KCNH2
SCHEMBL1951254 0.92 MET (0.81) METCDKL5KCNH2
SCHEMBL13623582 0.92 MET (0.84) METCDKL5KCNH2
Capmatinib SCHEMBL1427109 0.91 MET (0.98) METCDKL5KCNH2
Capmatinib SCHEMBL31061495 0.91 MET (0.98) METCDKL5KCNH2
Capmatinib SCHEMBL30166922 0.91 MET (0.98) METCDKL5KCNH2
Capmatinib SCHEMBL30166924 0.91 MET (0.98) METCDKL5KCNH2
Capmatinib SCHEMBL29362883 0.91 MET (0.97) METCDKL5KCNH2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10919901-B2 Imidazo[1,2-B][1,2,4]triazines as c-Met inhibitors INCYTE HOLDINGS CORPORATION (US) 2021-02-16 US disclosed
US-20200247811-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS INCYTE CORPORATION 2020-08-06 US disclosed
US-9988387-B2 Imidazo[1,2-B][1,2,4]triazines as c-Met inhibitors INCYTE HOLDINGS CORPORATION (US) 2018-06-05 US disclosed
EP-2531509-B1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS INCYTE HOLDINGS CORP (US) 2016-10-05 EP disclosed
US-20160137650-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS INCYTE CORPORATION 2016-05-19 US disclosed
US-9221824-B2 Imidazo[1,2-B][1,2,4]triazines as c-Met inhibitors INCYTE HOLDINGS CORPORATION (US) 2015-12-29 US disclosed
US-20130345224-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS INCYTE CORPORATION (US) 2013-12-26 US disclosed
US-8487096-B2 Imidazo[1,2-B][1,2,4]triazines as C-MET inhibitors INCYTE CORPORATION (US) 2013-07-16 US disclosed
US-20110212967-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS INCYTE CORPORATION (US) 2011-09-01 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-20130345224-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS MET, RET, ERBB2 MET 1/4885KCNH2 2816/4885CDKL5 498/4885
US-20110212967-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS MET, RET, ERBB2 MET 1/4885KCNH2 2816/4885CDKL5 498/4885
US-20200247811-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS MET, RET, ERBB2 MET 1/4885KCNH2 2816/4885CDKL5 498/4885
US-10919901-B2 Imidazo[1,2-B][1,2,4]triazines as c-Met inhibitors MET, RET, ERBB2 MET 1/4885KCNH2 2816/4885CDKL5 498/4885
US-20160137650-A1 IMIDAZO[1,2-B][1,2,4]TRIAZINES AS C-MET INHIBITORS MET, RET, ERBB2 MET 1/4885KCNH2 2816/4885CDKL5 498/4885

“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.