Hydrochloric Acid

Hydrochloric Acid

SCHEMBL630213

CC(N)Cc1c[nH]cn1.Cl.Cl

nearest known ligand 0.43

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 3/20 0.43
GLA known ✓ P06280 1/20 0.40
SLC6A2 known ✓ P23975 5/20 0.33
SLC6A3 known ✓ Q01959 3/20 0.33
SLC6A4 known ✓ P31645 2/20 0.33
MAOA known ✓ P21397 1/20 0.33
SIGMAR1 known ✓ Q99720 1/20 0.33
ADRB1 known ✓ P08588 1/20 0.33
HTR1A known ✓ P08908 1/20 0.33
ADRA2A known ✓ P08913 1/20 0.33
HTR1D known ✓ P28221 1/20 0.33
HTR1B known ✓ P28222 1/20 0.33
HTR2A known ✓ P28223 1/20 0.33
HTR2C known ✓ P28335 1/20 0.33
HTR1E known ✓ P28566 1/20 0.33
HTR7 known ✓ P34969 1/20 0.33
HTR2B known ✓ P41595 1/20 0.33
HTR6 known ✓ P50406 1/20 0.33
HRH4 Q9H3N8 3/20 0.43
ALDH1A1 P00352 2/20 0.43

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 SCHEMBL9700185 1.00 HRH4 (0.43) HRH4HRH3ALDH1A1LMNAAPEX1
Hydrochloric Acid SCHEMBL4609656 1.00 HRH4 (0.43) HRH4HRH3ALDH1A1LMNAAPEX1
Hydrochloric Acid SCHEMBL7111958 1.00 HRH4 (0.43) HRH4HRH3ALDH1A1LMNAAPEX1
SCHEMBL396350 0.98
SCHEMBL4008535 0.98
Bromide SCHEMBL1397996 0.96 HRH4 (0.40) HRH4HRH3ALDH1A1LMNAAPEX1
Bromide SCHEMBL4608777 0.96 HRH4 (0.40) HRH4HRH3ALDH1A1LMNAAPEX1
SCHEMBL14900011 0.82 DPP4 (0.35) HRH4HRH3ALDH1A1LMNAAPEX1
SCHEMBL19187383 0.82 DPP4 (0.35) HRH4HRH3ALDH1A1LMNAAPEX1
Choline SCHEMBL27844516 0.82 MEN1 (0.34) HRH4HRH3ALDH1A1LMNAAPEX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240277668-A1 HISTAMINE RECEPTOR AGONISTS FOR CANCER THERAPY IN CANCER PATIENTS UNRESPONSIVE TO CANCER IMMUNOTHERAPY AND WITH ELEVATED MYELOID DERIVED SUPPRESSOR CELLS TSP THERAPEUTICS INC. 2024-08-22 US claimed
EP-4376835-A1 HISTAMINE RECEPTOR AGONISTS FOR CANCER THERAPY IN CANCER PATIENTS UNRESPONSIVE TO CANCER IMMUNOTHERAPY AND WITH ELEVATED MYELOID DERIVED SUPPRESSOR CELLS TSP Therapeutics Inc. (US) 2024-06-05 EP claimed
US-20240165082-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT TSP THERAPEUTICS INC. 2024-05-23 US claimed
EP-4340838-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT Paz, Alberto (US) 2024-03-27 EP claimed
WO-2023009261-A1 HISTAMINE RECEPTOR AGONISTS FOR CANCER THERAPY IN CANCER PATIENTS UNRESPONSIVE TO CANCER IMMUNOTHERAPY AND WITH ELEVATED MYELOID DERIVED SUPPRESSOR CELLS PAZ ALBERTO (US) 2023-02-02 WO claimed
WO-2022245650-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT PAZ ALBERTO (US) 2022-11-24 WO claimed
EP-2419099-A2 COMPOSITION AND USE OF N-ALPHA-METHYLHISTAMINE Epicept Corporation (US) 2012-02-22 EP claimed
WO-2010120649-A2 COMPOSITION AND USE OF N-ALPHA-METHYLHISTAMINE DIHYDROCHLORIDE FOR THE REDUCTION OF OXYGEN RADICAL FORMATION EPICEPT CORPORATION (US) 2010-10-21 WO claimed
US-20240277668-A1 HISTAMINE RECEPTOR AGONISTS FOR CANCER THERAPY IN CANCER PATIENTS UNRESPONSIVE TO CANCER IMMUNOTHERAPY AND WITH ELEVATED MYELOID DERIVED SUPPRESSOR CELLS TSP THERAPEUTICS INC. 2024-08-22 US disclosed
EP-4376835-A1 HISTAMINE RECEPTOR AGONISTS FOR CANCER THERAPY IN CANCER PATIENTS UNRESPONSIVE TO CANCER IMMUNOTHERAPY AND WITH ELEVATED MYELOID DERIVED SUPPRESSOR CELLS TSP Therapeutics Inc. (US) 2024-06-05 EP disclosed
US-20240165082-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT TSP THERAPEUTICS INC. 2024-05-23 US disclosed
EP-4340838-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT Paz, Alberto (US) 2024-03-27 EP disclosed
WO-2023009261-A1 HISTAMINE RECEPTOR AGONISTS FOR CANCER THERAPY IN CANCER PATIENTS UNRESPONSIVE TO CANCER IMMUNOTHERAPY AND WITH ELEVATED MYELOID DERIVED SUPPRESSOR CELLS PAZ ALBERTO (US) 2023-02-02 WO disclosed
WO-2022245650-A1 ORALLY ADMINISTERED COMPOSITIONS FOR CANCER TREATMENT PAZ ALBERTO (US) 2022-11-24 WO disclosed
US-6166060-A 1H-4(5)-substituted imidazole derivatives GLIATECH, INC. (US) 2000-12-26 US disclosed
EP-0841922-A4 1H-4(5)-SUBSTITUTED IMIDAZOLE DERIVATIVES GLIATECH INC (US) 1999-03-10 EP disclosed
CN-1192144-A 1H-4(5)-substituted imidazole derivatives GLIATECH INC (US) 1998-09-02 CN disclosed
EP-0841922-A1 1H-4(5)-SUBSTITUTED IMIDAZOLE DERIVATIVES GLIATECH, INC. (US) 1998-05-20 EP disclosed
WO-1996038142-A1 1H-4(5)-SUBSTITUTED IMIDAZOLE DERIVATIVES GLIATECH, INC. (US) 1996-12-05 WO disclosed
US-5162541-A Using palladium containing catalysts and a hydrogen donor SCHERING CORPORATION (US) 1992-11-10 US disclosed