Hydrochloric Acid

Hydrochloric Acid

SCHEMBL28051575

Brc1ccc(-c2nc3ccccc3[nH]2)cc1.Cl

nearest known ligand 0.70

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 1/20 0.70
MMP8 known ✓ P22894 3/20 0.64
MMP13 known ✓ P45452 2/20 0.64
HDAC6 known ✓ Q9UBN7 1/20 0.61
NPC1 O15118 8/20 0.70
RAB9A P51151 8/20 0.70
KDM4E B2RXH2 8/20 0.67
ALDH1A1 P00352 8/20 0.67
SMN1; SMN2 Q16637 6/20 0.67
MAPT P10636 4/20 0.67
HPGD P15428 3/20 0.67
HSD17B10 Q99714 3/20 0.67
TP53 P04637 2/20 0.67
POLB P06746 1/20 0.67
GFER P55789 1/20 0.67
MMP2 P08253 3/20 0.64
MMP9 P14780 3/20 0.64
PKN1 Q16512 1/20 0.64
PKN2 Q16513 1/20 0.64
KMT2A Q03164 1/20 0.62

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
SCHEMBL481735 0.98 NPC1 (0.72) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL13942807 0.96 NPC1 (0.70) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL2178266 0.89 NPC1 (0.88) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL29386825 0.89 NPC1 (0.88) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL24295036 0.87 NPC1 (0.84) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL22499602 0.85 NPC1 (0.81) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL2763186 0.85 CA12 (0.59) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL17393603 0.84 NR1H4 (0.61) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL2252555 0.83 NPC1 (0.92) NPC1RAB9AGAAKDM4EALDH1A1
SCHEMBL6503052 0.83 HPSE (0.87) NPC1RAB9AKDM4ESMN1; SMN2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105646591-B It is a kind of using brominated benzimidazole as blue light complex of iridium of cyclic metal complexes and preparation method thereof 福建师范大学 2018-10-19 CN claimed
CN-105646591-A Blue light iridium complex taking bromine-contained benzimidazoles as cyclometalated ligands and preparation method of blue light iridium complex 福建师范大学 2016-06-08 CN claimed
CN-105524115-A Red light iridium complex with bromine-containing benzimidazole as cyclometalated ligand and preparation method thereof UNIV FUJIAN 2016-04-27 CN claimed
CN-105399778-A Green-light iridium complex with bromine-containing benzimidazoles as cyclometalated ligand and preparation method thereof UNIV FUJIAN 2016-03-16 CN claimed
CN-105646591-B It is a kind of using brominated benzimidazole as blue light complex of iridium of cyclic metal complexes and preparation method thereof 福建师范大学 2018-10-19 CN disclosed
CN-105646591-A Blue light iridium complex taking bromine-contained benzimidazoles as cyclometalated ligands and preparation method of blue light iridium complex 福建师范大学 2016-06-08 CN disclosed
CN-105524115-A Red light iridium complex with bromine-containing benzimidazole as cyclometalated ligand and preparation method thereof UNIV FUJIAN 2016-04-27 CN disclosed
CN-105399778-A Green-light iridium complex with bromine-containing benzimidazoles as cyclometalated ligand and preparation method thereof UNIV FUJIAN 2016-03-16 CN disclosed