Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3504243

Cl.Cl.Cl.Cl.Nc1ccc(-c2ccc(N)c(N)c2N)cc1.O.O

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
PRKCZ known ✓ Q05513 1/20 0.32
MAOA known ✓ P21397 1/20 0.31
MAOB known ✓ P27338 1/20 0.31
CA2 known ✓ P00918 1/20 0.31
FLT3 known ✓ P36888 3/20 0.31
KIT known ✓ P10721 2/20 0.31
KDR known ✓ P35968 2/20 0.31
GAA known ✓ P10253 1/20 0.30
JAK2 known ✓ O60674 1/20 0.30
ABL1 known ✓ P00519 1/20 0.30
NTRK1 known ✓ P04629 1/20 0.30
RET known ✓ P07949 1/20 0.30
MET known ✓ P08581 1/20 0.30
NTRK2 known ✓ Q16620 1/20 0.30
ALDH1A1 P00352 4/20 0.43
CYP3A4 P08684 3/20 0.43
TDP1 Q9NUW8 3/20 0.43
TP53 P04637 3/20 0.43
HSD17B10 Q99714 3/20 0.37
TAAR1 Q96RJ0 2/20 0.37

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 SCHEMBL28663126 1.00 ALDH1A1 (0.43) ALDH1A1CYP3A4TDP1TP53HSD17B10
Hydrochloric Acid SCHEMBL28335260 1.00 ALDH1A1 (0.43) ALDH1A1CYP3A4TDP1TP53HSD17B10
Hydrochloric Acid SCHEMBL992776 0.98 CYP3A4 (0.46) ALDH1A1CYP3A4TDP1TP53HSD17B10
Water SCHEMBL7066183 0.98 TDP1 (0.46) ALDH1A1CYP3A4TDP1TP53HSD17B10
Hydrochloric Acid SCHEMBL999548 0.98 CYP3A4 (0.46) ALDH1A1CYP3A4TDP1TP53HSD17B10
Hydrochloric Acid SCHEMBL134929 0.98 CYP3A4 (0.46) ALDH1A1CYP3A4TDP1TP53HSD17B10
SCHEMBL21373 0.95 TDP1 (0.48) ALDH1A1CYP3A4TDP1TP53HSD17B10
SCHEMBL5983370 0.95 TDP1 (0.48) ALDH1A1CYP3A4TDP1TP53HSD17B10
SCHEMBL30272720 0.95 TDP1 (0.48) ALDH1A1CYP3A4TDP1TP53HSD17B10
SCHEMBL3507048 0.93 TDP1 (0.46) ALDH1A1CYP3A4TDP1TP53HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4816387-A ELECTROPHORESIS, COLORIMETRIC ANALYSIS BIO-RESEARCH LABORATORIES, INC. (US) 1989-03-28 US claimed
WO-1987007647-A1 METHOD FOR DETECTION OF ANTIBODIES TO HTLV-III VIRUS AND DIAGNOSTIC TEST KIT USEFUL THEREWITH TEXAS BIO-RESEARCH LABORATORIES, INC. (US) 1987-12-17 WO claimed
WO-2023076921-A1 METHODS FOR ENHANCED BCMA IMMUNOHISTOCHEMISTRY DETECTION IN HUMAN AND MONKEY TISSUE JANSSEN BIOTECH, INC. (US) 2023-05-04 WO disclosed
US-9097716-B2 Assay for anti-TR antibodies ERASMUS UNIVERSITY MEDICAL CENTER (NL) 2015-08-04 US disclosed
US-20150050668-A1 ASSAY FOR ANTI-TR ANTIBODIES ERASMUS UNIVERSITY MEDICAL CENTER ROTTERDAM (NL) 2015-02-19 US disclosed
US-8883745-B2 C—glycolipids with enhanced Th-1 profile NEW YORK UNIVERSITY (US) 2014-11-11 US disclosed
WO-2013129913-A1 ASSAY FOR ANTI - TR ANTIBODIES ERASMUS UNIVERSITY MEDICAL CENTER ROTTERDAM (NL) 2013-09-06 WO disclosed
CN-101500580-B C-glycolipids with enhanced Th-1 profile NEW YORK UNIVERSITY (US) 2011-12-07 CN disclosed
US-20100233207-A1 C-GLYCOLIPIDS WITH ENHANCED TH-1 PROFILE NEW YORK UNIVERSITY (US) 2010-09-16 US disclosed
CN-101500580-A C-glycolipids with enhanced Th-1 profile UNIV NEW YORK (US) 2009-08-05 CN disclosed
WO-2009040136-A1 METHODS AND COMPOSITIONS TO TREAT AQUATIC ORGANISMS GHENT UNIVERSITY (BE) 2009-04-02 WO disclosed
US-5583102-A ADMINISTERING TO STIMULATE WOUND REGENERATION, DECREASE SCAR FORMATION UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 1996-12-10 US disclosed
EP-0324834-B1 METHOD FOR RAPID AND SENSITIVE DETECTION OF HIV-I ANTIBODIES VERIGEN INC (US) 1995-11-08 EP disclosed
EP-0324834-A4 METHOD FOR RAPID AND SENSITIVE DETECTION OF HIV-I ANTIBODIES 1992-05-06 EP disclosed
US-4885235-A ELECTROPHORETICALLY RESOLVED HIV-I ANTIGEN IS INCUBATED IN THE PRESENCE OF MILK PROTEIN 501 BIO-RESEARCH LABORATORIES, INC. (US) 1989-12-05 US disclosed
EP-0324834-A1 METHOD FOR RAPID AND SENSITIVE DETECTION OF HIV-I ANTIBODIES VERIGEN, INC. (US) 1989-07-26 EP disclosed
US-4816387-A ELECTROPHORESIS, COLORIMETRIC ANALYSIS BIO-RESEARCH LABORATORIES, INC. (US) 1989-03-28 US disclosed
WO-1989000207-A1 METHOD FOR RAPID AND SENSITIVE DETECTION OF HIV-I ANTIBODIES BIO RES LAB INC (US) 1989-01-12 WO disclosed
US-4792520-A Methods and kits for identifying mutagenic agents and molecular mutations in DNA in mammalian cells UNIVERSITY OF CINCINNATI (US) 1988-12-20 US disclosed
WO-1987007647-A1 METHOD FOR DETECTION OF ANTIBODIES TO HTLV-III VIRUS AND DIAGNOSTIC TEST KIT USEFUL THEREWITH TEXAS BIO-RESEARCH LABORATORIES, INC. (US) 1987-12-17 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-20100233207-A1 C-GLYCOLIPIDS WITH ENHANCED TH-1 PROFILE ICOS, CD69, TSLP PRKCZ 2146/4885MAOA 4512/4885MAOB 4346/4885

“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.