Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4340573

Cl.[Pt].c1ccc(-n2cccn2)c(-n2cccn2)c1

nearest known ligand 0.62

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 0.54
ADRA2A known ✓ P08913 1/20 0.45
ADRA1A known ✓ P35348 1/20 0.45
CHRM1 known ✓ P11229 1/20 0.40
KCNA5 known ✓ P22460 1/20 0.39
GLA known ✓ P06280 1/20 0.38
DRD2 known ✓ P14416 1/20 0.36
DRD4 known ✓ P21917 1/20 0.36
DRD3 known ✓ P35462 1/20 0.36
HCRTR1 known ✓ O43613 1/20 0.35
HCRTR2 known ✓ O43614 1/20 0.35
MAPK1 P28482 3/20 0.62
NPC1 O15118 2/20 0.62
ALDH1A1 P00352 4/20 0.54
KDM4E B2RXH2 3/20 0.54
MAPT P10636 2/20 0.54
LMNA P02545 2/20 0.54
MEN1 O00255 1/20 0.54
G6PD P11413 1/20 0.54
KMT2A Q03164 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 SCHEMBL4336588 0.98 MAPK1 (0.64) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL4332969 0.98 MAPK1 (0.64) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL4341886 0.95 MAPK1 (0.67) MAPK1NPC1ALDH1A1KDM4EMAPT
Hydrochloric Acid SCHEMBL4340576 0.93 MAPK1 (0.64) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL255914 0.80 MAPK1 (0.56) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL16291306 0.80 MAPK1 (0.56) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL1531523 0.80 MAPK1 (0.56) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL255339 0.80 MAPK1 (0.56) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL20205325 0.80 MAPK1 (0.56) MAPK1NPC1ALDH1A1KDM4EMAPT
SCHEMBL206362 0.80 KDM4E (0.64) MAPK1NPC1ALDH1A1KDM4EMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110301351-A1 Platinum (II) Di (2-Pyrazolyl) Benzene Chloride Analogs and Uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-12-08 US claimed
WO-2009086209-A2 PLATINUM(II) DI(2-PYRAZOLYL)BENZENE CHLORIDE ANALOGS AND USES ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2009-07-09 WO claimed
US-9082989-B2 Platinum (II) di (2-pyrazolyl) benzene chloride analogs and uses Arizona Board of Regents for and on behalf of Arizona State Univesity (US) 2015-07-14 US disclosed
US-9082989-B2 Platinum (II) di (2-pyrazolyl) benzene chloride analogs and uses Arizona Board of Regents for and on behalf of Arizona State Univesity (US) 2015-07-14 US disclosed
US-8846940-B2 Platinum (II) di (2-pyrazolyl) benzene chloride analogs and uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2014-09-30 US disclosed
US-8846940-B2 Platinum (II) di (2-pyrazolyl) benzene chloride analogs and uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2014-09-30 US disclosed
US-20140066628-A1 Platinum (II) Di (2-Pyrazolyl) Benzene Chloride Analogs and Uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2014-03-06 US disclosed
US-20140066628-A1 Platinum (II) Di (2-Pyrazolyl) Benzene Chloride Analogs and Uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2014-03-06 US disclosed
US-20110301351-A1 Platinum (II) Di (2-Pyrazolyl) Benzene Chloride Analogs and Uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-12-08 US disclosed
US-20110301351-A1 Platinum (II) Di (2-Pyrazolyl) Benzene Chloride Analogs and Uses ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2011-12-08 US disclosed
WO-2009086209-A3 PLATINUM(II) DI(2-PYRAZOLYL)BENZENE CHLORIDE ANALOGS AND USES ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2009-10-08 WO disclosed
WO-2009086209-A2 PLATINUM(II) DI(2-PYRAZOLYL)BENZENE CHLORIDE ANALOGS AND USES ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2009-07-09 WO disclosed
WO-2009086209-A2 PLATINUM(II) DI(2-PYRAZOLYL)BENZENE CHLORIDE ANALOGS AND USES ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2009-07-09 WO 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 (1 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-20110301351-A1 Platinum (II) Di (2-Pyrazolyl) Benzene Chloride Analogs and Uses PDCD1LG2, PDCD2L, IDH1 GAA 4558/4885ADRA2A 3639/4885ADRA1A 4514/4885

“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.