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 SCHEMBL1784388 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL331304 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL2798048 | 1.00 | — | — | |
| Bromide SCHEMBL7458836 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL1827545 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL8679917 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL10917278 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL619693 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL6995881 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL11676046 | 0.82 | — | — |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20160083345-A1 | POLYMORPHIC FORMS OF LOMITAPIDE AND ITS SALTS AND PROCESSES FOR THEIR PREPARATION | CADILA HEALTHCARE LIMITED (IN) | 2016-03-24 | — | — | US | claimed |
| WO-2012001486-A1 | AN IMPROVED PROCESS FOR THE PREPARATION OF PRASUGREL HYDROCHLORIDE AND ITS INTERMEDIATES | MAYUKA LABS PVT. LTD. (IN) | 2012-01-05 | — | — | WO | claimed |
| US-4376080-A | HYDROGEN CYANIDE AND DIAZOACETONITRILE; CATALYTIC COPPER COMPOUND | UBE INDUSTRIES, LTD. (JP) | 1983-03-08 | — | — | US | claimed |
| US-4053530-A | REACTING AMMONIUM BIFLUORIDE WITH CARBON TETRACHLORIDE OR CHLOROFORM USING 2A, FERRIC, OR CHROMIC FLUORIDES AS A CATALYST | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1977-10-11 | — | — | US | claimed |
| JP-61292864-A | — | — | None | — | — | JP | disclosed |
| US-9072721-B2 | Composition for preventing or treating immune-related disease and oxidative-stress-related disease | Kim, Hak Bum (KR) | 2015-07-07 | — | — | US | disclosed |
| WO-2012001486-A1 | AN IMPROVED PROCESS FOR THE PREPARATION OF PRASUGREL HYDROCHLORIDE AND ITS INTERMEDIATES | MAYUKA LABS PVT. LTD. (IN) | 2012-01-05 | — | — | WO | disclosed |
| EP-2066644-A2 | SALTS OF ROSUVASTATIN AND PROCESSES FOR THEIR PREPARATION | Glenmark Pharmaceuticals Limited (IN) | 2009-06-10 | — | — | EP | disclosed |
| WO-2008015563-A2 | SALTS OF ROSUVASTATIN AND PROCESSES FOR THEIR PREPARATION | GLENMARK PHARMACEUTICALS LIMITED (US) | 2008-02-07 | — | — | WO | disclosed |
| US-6375857-B1 | Method to form fuse using polymeric films | CHARTERED SEMICONDUCTOR MANUFACTURING LTD. (TW) | 2002-04-23 | — | — | US | disclosed |
| EP-0447055-B1 | 3-(Substituted phenyl)pyrazole derivatives, a process for producing the same, herbicidal composition containing the same and method of controlling weeds using said composition | NIHON NOHYAKU CO LTD (JP) | 1998-07-08 | — | — | EP | disclosed |
| US-5698585-A | FOR SENILE CATARACT CAUSED BY OXIDATION DISORDER; VISION DEFECTS | KIKKOMAN CORPORATION (JP) | 1997-12-16 | — | — | US | disclosed |
| US-4284783-A | Liquid phase preparation of 2-chloro-5-trifluoromethylpyridine and 2-chloro-5-perchlorofluoromethylpyridine | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1981-08-18 | — | — | US | disclosed |
| US-4257857-A | Liquid phase preparation of 2-chloro-5-trifluoromethylpyridine and 2-chloro-5-perchlorofluoromethylpyridine | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1981-03-24 | — | — | US | disclosed |
| US-4172104-A | DISSOLVING ETHOXYLATE OF FATTY ALCOHOL IN CHLORINATED HYDROCARBON SOLVENT, PRECIPITATION BY TREATMENT WITH STEAM OR HOT WATER | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1979-10-23 | — | — | US | disclosed |
| US-4169105-A | FROM CYANOACETIC ACID AND AN ALLYLIC HALIDE, ACID ACCEPTOR | SHELL OIL COMPANY (US) | 1979-09-25 | — | — | US | disclosed |
| US-4151162-A | Diazomerocyanines and mesomeric forms thereof | L'OREAL (FR) | 1979-04-24 | — | — | US | disclosed |
| US-4122249-A | ALIPHATIC CARBOXYLIC ACID, ALCOHOL, ESTER OR AMIDE LUBRICANT | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1978-10-24 | — | — | US | disclosed |
| US-4107377-A | Process for producing 3-trichloromethyl-5-loweralkylamino-1,2,4-thiadiazole | OLIN CORPORATION (US) | 1978-08-15 | — | — | US | disclosed |
| US-3985499-A | Diazamerocyanines for dyeing keratinous fibers | L'OREAL (FR) | 1976-10-12 | — | — | US | disclosed |