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.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL23888654 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL28348663 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL27671528 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL29157768 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL28257143 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL6286035 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL27882916 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL27481144 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL6444953 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL27914669 | 0.91 | — | — |
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.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-1927725-A | Process of preparing atomic energy level zirconium dioxide and hafnium oxide by methyl isobutanone double solvent extraction method | JIANGXI KINGAN HI TECH CO LTD (CN) | 2007-03-14 | — | — | CN | claimed |
| US-9561493-B2 | Synthesis of pyrochlore nanostructures and uses thereof | BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA, RENO (US) | 2017-02-07 | — | — | US | disclosed |
| US-20150080213-A1 | Synthesis of Pyrochlore Nanostructures and Uses Thereof | BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA (US) | 2015-03-19 | — | — | US | disclosed |
| CN-103149284-B | Tigecycline side chain intermediate detecting method | CHENGDU BAIYU SCIENCE & TECHNOLOGY PHARMACEUTICAL CO LTD | 2014-12-10 | — | — | CN | disclosed |
| US-8900537-B2 | Synthesis of pyrochlore nanostructures and uses thereof | BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA, RENO (US) | 2014-12-02 | — | — | US | disclosed |
| CN-103091424-B | Methods for detecting impurities in tigecycline | CHENGDU BAIYU SCIENCE & TECHNOLOGY PHARMACEUTICAL CO LTD | 2014-11-19 | — | — | CN | disclosed |
| US-8889772-B2 | Method for producing mixtures of alkylphosphonous acid salts and dialkylphosphinic acid salts | CLARIANT FINANCE (BVI) LIMITED (VG) | 2014-11-18 | — | — | US | disclosed |
| CN-103149284-A | Tigecycline side chain intermediate detecting method | CHENGDU BAIYU TECHNOLOGY PHARMACEUTICAL CO LTD | 2013-06-12 | — | — | CN | disclosed |
| US-20130126805-A1 | Method For Producing Alkylphosphonous Acid Salts | CLARIANT FINANCE (BVI) LIMITED (VG) | 2013-05-23 | — | — | US | disclosed |
| US-20130131239-A1 | Method for Producing Mixtures of Alkylphosphonous Acid Salts And Dialkylphosphinic Acid Salts | CLARIANT FINANCE (BVI) LIMITED (VG) | 2013-05-23 | — | — | US | disclosed |
| US-20110281111-A1 | SYNTHESIS OF PYROCHLORE NANOSTRUCTURES AND USES THEREOF | BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA, (US) | 2011-11-17 | — | — | US | disclosed |
| US-7635785-B2 | Process for preparation of dialkylphosphinic salts | Clariant Deutschland GmbH (DE) | 2009-12-22 | — | — | US | disclosed |
| US-7622517-B2 | flame retardant formulation for cellulose-containing moldings ( paperboard, textile, wood), comprising dicyandiamide-formaldehyde resin and a diphoshinic salt of a metal selected from Mg, Ca, Al, Sb, Sn, Ge, Ti, Fe, Zr, Ce, Bi, Sr, Mn, Li | CLARIANT PRODUKTE (DEUTSCHLAND) GMBH (DE) | 2009-11-24 | — | — | US | disclosed |
| US-20090005471-A1 | Phosphorus-containing flame retardant formulation for cellulose-containing moldings | CLARIANT PRODUKTE (DEUTSCHLAND) GMBH | 2009-01-01 | — | — | US | disclosed |
| US-20070213563-A1 | Mixtures composed of monocarboxy-functionalized dialkylphosphinic acid salts, their use und a process for their preparation | CLARIANT INTERNATIONAL LTD | 2007-09-13 | — | — | US | disclosed |
| US-20050222309-A1 | Phosphorus-containing flame retardant formulation for cellulose-containing moldings | CLARIANT GMBH | 2005-10-06 | — | — | US | disclosed |
| US-20050137418-A1 | Process for preparation of dialkylphosphinic salts | CLARIANT GMBH | 2005-06-23 | — | — | US | disclosed |
| EP-0042702-B1 | PROCESS FOR THE RECOVERY OF LEAD AND SILVER FROM MINERALS AND PROCESS RESIDUES | Provincial Holdings Ltd. (CA) | 1984-09-26 | — | — | EP | disclosed |
| US-4372782-A | Recovery of lead and silver from minerals and process residues | PROVINCIAL HOLDINGS LTD. (CA) | 1983-02-08 | — | — | US | disclosed |
| EP-0042702-A1 | Process for the recovery of lead and silver from minerals and process residues | Provincial Holdings Ltd. (CA) | 1981-12-30 | — | — | EP | disclosed |