Hydrochloric Acid

Hydrochloric Acid

SCHEMBL999376

Cl.c1ccc2cc3c(ccc4[nH]ncc43)cc2c1

nearest known ligand 0.47

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
HSP90AA1 known ✓ P07900 1/20 0.47
FGFR1 known ✓ P11362 1/20 0.42
IDO1 P14902 2/20 0.47
CDK2 P24941 1/20 0.47
METAP2 P50579 5/20 0.42
DYRK3 O43781 1/20 0.42
CLK1 P49759 1/20 0.42
CLK2 P49760 1/20 0.42
CLK3 P49761 1/20 0.42
GSK3B P49841 1/20 0.42
CDK5 Q00535 1/20 0.42
DYRK1A Q13627 1/20 0.42
CDK5R1 Q15078 1/20 0.42
DYRK2 Q92630 1/20 0.42
CLK4 Q9HAZ1 1/20 0.42
DYRK1B Q9Y463 1/20 0.42
ALDH1A1 P00352 1/20 0.42
HIF1A Q16665 1/20 0.42
CYP1B1 Q16678 1/20 0.42
HSD17B10 Q99714 1/20 0.42

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
SCHEMBL30486 0.98 IDO1 (0.48) IDO1HSP90AA1CDK2METAP2FGFR1
Pyrrole SCHEMBL27612136 0.90 IDO1 (0.42) IDO1HSP90AA1CDK2METAP2FGFR1
SCHEMBL4141797 0.83 RAF1 (0.40) IDO1HSP90AA1CDK2MKNK1
SCHEMBL17255318 0.81 HASPIN (0.45) FGFR1CLK1DYRK1A
SCHEMBL276443 0.81 IDO1 (0.54) IDO1HSP90AA1CDK2METAP2FGFR1
SCHEMBL29563426 0.81 IDO1 (0.54) IDO1HSP90AA1CDK2METAP2FGFR1
SCHEMBL29450787 0.78 HPRT1 (0.54) IDO1HSP90AA1CDK2METAP2ALDH1A1
SCHEMBL27074503 0.78 HPRT1 (0.54) IDO1HSP90AA1CDK2METAP2ALDH1A1
SCHEMBL7208201 0.78 PTPRC (0.41) IDO1ALDH1A1KDM4EMEN1MAPT
SCHEMBL12321248 0.76 NOS1 (0.56) IDO1HSP90AA1CDK2METAP2DYRK3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7901453-B2 Coated implantable medical device COOK INCORPORATED (US) 2011-03-08 US claimed
US-20080145399-A1 coronary stent has a multilayer coatings for controlled release of immunosuppressive agent active materials, including a porous cover layer COOK MEDICAL TECHNOLOGIES LLC 2008-06-19 US claimed
US-20080145398-A1 coronary stent has a multilayer coatings for controlled release of immunosuppressive agent active materials, including a porous cover layer WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2008-06-19 US claimed
US-20030036794-A1 Coated implantable medical device COOK INCORPORATED 2003-02-20 US claimed
US-8313521-B2 Method of delivering an implantable medical device with a bioabsorbable coating COOK MEDICAL TECHNOLOGIES LLC (US) 2012-11-20 US disclosed
US-8257433-B2 Coated implantable medical device COOK MEDICAL TECHNOLOGIES LLC (US) 2012-09-04 US disclosed
US-7901453-B2 Coated implantable medical device COOK INCORPORATED (US) 2011-03-08 US disclosed
US-7862605-B2 Coated implantable medical device MED INSTITUTE, INC. (US) 2011-01-04 US disclosed
US-20100196439-A1 Angiogenesis Mechanism and Method, and Implantable Device MEDTRONIC, INC. (US) 2010-08-05 US disclosed
US-7611533-B2 Coated implantable medical device COOK INCORPORATED (US) 2009-11-03 US disclosed
WO-2009004496-A2 BISANTHRAPYRAZOLES AS ANTI-CANCER AGENTS UNIVERSITY OF MANITOBA (US) 2009-01-08 WO disclosed
US-7445628-B2 Method of treating a patient with a coated implantable medical device COOK INCORPORATED (US) 2008-11-04 US disclosed
US-20080145399-A1 coronary stent has a multilayer coatings for controlled release of immunosuppressive agent active materials, including a porous cover layer COOK MEDICAL TECHNOLOGIES LLC 2008-06-19 US disclosed
US-20080145398-A1 coronary stent has a multilayer coatings for controlled release of immunosuppressive agent active materials, including a porous cover layer WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2008-06-19 US disclosed
US-20070168012-A1 Coated implantable medical device MED INSTITUTE, INC. (US) 2007-07-19 US disclosed
US-20070150047-A1 Implantable medical device with bioabsorbable coating MED INSTITUTE, INC. (US) 2007-06-28 US disclosed
WO-2007047539-A2 LOCALIZED DELIVERY TO THE LYMPHATIC SYSTEM MEDTRONIC, INC. (US) 2007-04-26 WO disclosed
US-20070087029-A1 Localized delivery to the lymphatic system MEDTRONIC, INC. 2007-04-19 US disclosed
US-20040047909-A1 Providing a structure comprising a base material; positioning a bioactive agent; positioning at least one porous layer over bioactive, porous layer being of a thickness adequate to provide a controlled release of bioactive agent COOK MEDICAL TECHNOLOGIES LLC 2004-03-11 US disclosed
US-20030036794-A1 Coated implantable medical device COOK INCORPORATED 2003-02-20 US disclosed