Hydrochloric Acid

Hydrochloric Acid

SCHEMBL10522176

Cl.Cl.Cl.Cl.O=C1c2c(O)ccc(O)c2C(=O)c2c(NCCNCCNCCO)ccc(NCCNCCNCCO)c21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
TOP2A known ✓ P11388 2/20 0.97
CACNA1F known ✓ O60840 1/20 0.97
EGFR known ✓ P00533 1/20 0.97
ESR1 known ✓ P03372 1/20 0.97
ERBB2 known ✓ P04626 1/20 0.97
CHRM2 known ✓ P08172 1/20 0.97
CHRM4 known ✓ P08173 1/20 0.97
CHRM1 known ✓ P11229 1/20 0.97
SLC6A2 known ✓ P23975 1/20 0.97
HRH2 known ✓ P25021 1/20 0.97
HTR2C known ✓ P28335 1/20 0.97
ADRA1A known ✓ P35348 1/20 0.97
PTGS2 known ✓ P35354 1/20 0.97
DRD3 known ✓ P35462 1/20 0.97
OPRK1 known ✓ P41145 1/20 0.97
HTR2B known ✓ P41595 1/20 0.97
CACNA1D known ✓ Q01668 1/20 0.97
KCNH2 known ✓ Q12809 1/20 0.97
CACNA1S known ✓ Q13698 1/20 0.97
CACNA1C known ✓ Q13936 1/20 0.97

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
Mitoxantrone SCHEMBL29462659 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Hydrochloric Acid SCHEMBL11305688 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL29366412 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL1256885 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Hydrochloric Acid SCHEMBL11039686 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL532914 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL66384 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL3928 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Mitoxantrone SCHEMBL2342900 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA
Hydrochloric Acid SCHEMBL11278695 1.00 MEN1 (1.00) MEN1KMT2AMAPK1TDP1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4820738-A ANTITUMOR AGENTS; CHELATING AGENTS; GROWTH INHIBITORS; LEUKEMIA AMERICAN CYANAMID COMPANY (US) 1989-04-11 US disclosed
US-4614618-A CHELATING AGENTS AND ANTICANCER AGENTS AMERICAN CYANAMID COMPANY (US) 1986-09-30 US disclosed
US-4540519-A CHELATE COMPOUNDS, ANTICANCER AGENTS AMERICAN CYANAMID COMPANY (US) 1985-09-10 US disclosed
US-4526989-A And ascorbic acid salt AMERICAN CYANAMID COMPANY (US) 1985-07-02 US disclosed
US-4456552-A CHELATION, ANTITUMOR AMERICAN CYANAMID COMPANY (US) 1984-06-26 US disclosed
US-4430501-A CHELATION, ANTITUMOR, COMPLEXING, SEQUESTERING AMERICAN CYANAMID COMPANY (US) 1984-02-07 US disclosed
EP-0037486-B1 METAL CHELATES OF 1,4-BIS(SUBSTITUTED-AMINO)-5,8-DIHYDROXY-ANTHRAQUINONES AMERICAN CYANAMID COMPANY (US) 1984-01-25 EP disclosed
US-4296030-A ANTITUMOR AGENTS, DYES AMERICAN CYANAMID COMPANY (US) 1981-10-20 US disclosed
EP-0037486-A2 Metal chelates of 1,4-bis(substituted-amino)-5,8-dihydroxy-anthraquinones AMERICAN CYANAMID COMPANY (US) 1981-10-14 EP disclosed
US-4278689-A ANTITUMOR AGENTS AMERICAN CYANAMID COMPANY (US) 1981-07-14 US disclosed
US-4197249-A ANTITUMOR AGENTS AMERICAN CYANAMID COMPANY (US) 1980-04-08 US disclosed