Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6018896

Cl.Cl.NCc1cccc(CN)c1

nearest known ligand 0.67

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
HRH3 known ✓ Q9Y5N1 1/20 0.50
MAOB known ✓ P27338 1/20 0.46
GRIN2D known ✓ O15399 1/20 0.46
GRIN3B known ✓ O60391 1/20 0.46
GRIN1 known ✓ Q05586 1/20 0.46
GRIN2A known ✓ Q12879 1/20 0.46
GRIN2B known ✓ Q13224 1/20 0.46
GRIN2C known ✓ Q14957 1/20 0.46
GRIN3A known ✓ Q8TCU5 1/20 0.46
LOXL2 Q9Y4K0 4/20 0.67
PNMT P11086 1/20 0.64
ENPP2 Q13822 1/20 0.64
NOS1 P29475 6/20 0.57
NOS2 P35228 6/20 0.57
NOS3 P29474 4/20 0.57
ALDH1A1 P00352 2/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
PRMT6 Q96LA8 1/20 0.56
CYP3A4 P08684 1/20 0.54
NFKB1 P19838 1/20 0.54

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 SCHEMBL8195914 1.00 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
SCHEMBL10422276 0.97 LOXL2 (0.71) LOXL2PNMTENPP2NOS1NOS2
SCHEMBL36008 0.97 LOXL2 (0.71) LOXL2PNMTENPP2NOS1NOS2
Bromide SCHEMBL28362115 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
SCHEMBL29013584 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
Water SCHEMBL28545356 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
Ammonia Solution, Strong SCHEMBL6899866 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
SCHEMBL7883952 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
Iodide SCHEMBL29198612 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2
Bromide SCHEMBL29013587 0.94 LOXL2 (0.67) LOXL2PNMTENPP2NOS1NOS2

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
US-10882955-B2 Ammonium salt catalyzed benzoxazine polymerization 3M INNOVATIVE PROPERTIES COMPANY (US) 2021-01-05 US disclosed
US-20180162999-A1 AMMONIUM SALT CATALYZED BENZOXAZINE POLYMERIZATION 3M INNOVATIVE PROPERTIES COMPANY 2018-06-14 US disclosed
CN-102503835-A Synthetic method for ammonium salt MEI LUO 2012-06-20 CN disclosed
CN-102329240-A Method for preparing and synthesizing m-xylylenediamine dihydrochloride MEI LUO 2012-01-25 CN disclosed
CN-102329240-A Method for preparing and synthesizing m-xylylenediamine dihydrochloride MEI LUO 2012-01-25 CN disclosed
EP-1569982-B1 METHOD OF PREPARING HIGH MOLECULAR WEIGHT RANDOM POLYHYDROXYPOLYAMIDES UNIV MONTANA (US) 2006-09-13 EP disclosed
EP-1569982-A1 METHOD OF PREPARING HIGH MOLECULAR WEIGHT RANDOM POLYHYDROXYPOLYAMIDES THE UNIVERSITY OF MONTANA (US) 2005-09-07 EP disclosed
WO-2004052959-A1 METHOD OF PREPARING HIGH MOLECULAR WEIGHT RANDOM POLYHYDROXYPOLYAMIDES THE UNIVERSITY OF MONTANA (US) 2004-06-24 WO disclosed