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)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | OPRM1 known ✓ | P35372 | 1/20 | 0.46 |
| ▸ | SPHK1 | Q9NYA1 | 2/20 | 0.43 |
| ▸ | DNM1 | Q05193 | 4/20 | 0.39 |
| ▸ | LMNA | P02545 | 2/20 | 0.38 |
| ▸ | TP53 | P04637 | 2/20 | 0.38 |
| ▸ | CYP2D6 | P10635 | 2/20 | 0.36 |
| ▸ | ADH1B | P00325 | 1/20 | 0.36 |
| ▸ | ADH1C | P00326 | 1/20 | 0.36 |
| ▸ | ADH1A | P07327 | 1/20 | 0.36 |
| ▸ | ADH4 | P08319 | 1/20 | 0.36 |
| ▸ | ADH7 | P40394 | 1/20 | 0.36 |
| ▸ | PLA2G1B | P04054 | 1/20 | 0.36 |
| ▸ | PLA2G2A | P14555 | 1/20 | 0.36 |
| ▸ | GMNN | O75496 | 1/20 | 0.36 |
| ▸ | POLB | P06746 | 1/20 | 0.36 |
| ▸ | THPO | P40225 | 1/20 | 0.36 |
| ▸ | MTOR | P42345 | 1/20 | 0.36 |
| ▸ | BLM | P54132 | 1/20 | 0.36 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.36 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.36 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL15823526 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL3101949 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL3104729 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL634994 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL9420650 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL1254112 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL637396 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL5138752 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL534401 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 | |
| Hydrochloric Acid SCHEMBL8357940 | 1.00 | OPRM1 (0.46) | OPRM1SPHK1DNM1LMNATP53 |
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 483 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119591470-A | Perfluoro-3-methyl-2-pentene and preparation method and application thereof | 浙江巨化技术中心有限公司 | 2025-03-11 | — | — | CN | claimed |
| US-20240191084-A1 | ANTIMICROBIAL AND ANTIVIRAL BUILDING PANELS | ARMSTRONG WORLD INDUSTRIES, INC. | 2024-06-13 | — | — | US | claimed |
| EP-3408883-B1 | METHOD OF PREPARING BATTERY ELECTRODES | GRST INT LTD (CN) | 2024-05-08 | — | — | EP | claimed |
| EP-3294750-B1 | COMPOSITION AND METHODS FOR EXTRACTING MYCOTOXINS | WATERS TECHNOLOGIES CORP (US) | 2023-10-25 | — | — | EP | claimed |
| EP-3836253-A1 | METHOD OF PREPARING BATTERY ELECTRODES | GRST International Limited (CN) | 2021-06-16 | — | — | EP | claimed |
| CN-107431193-B | Method for preparing battery electrode | 皓智环球有限公司 | 2021-05-04 | — | — | CN | claimed |
| CN-107342392-B | Method for preparing battery electrode | 皓智环球有限公司 | 2021-03-09 | — | — | CN | claimed |
| CN-112301745-A | Oil agent for continuous spunbond fibers and preparation method and application thereof | 沈阳浩博实业有限公司 | 2021-02-02 | — | — | CN | claimed |
| CN-109678871-B | Method for preparing bisbenzylisoquinoline compounds | 山东师范大学 | 2020-09-29 | — | — | CN | claimed |
| US-10563347-B2 | Antibacterial/antifungal finished product production method, and antibacterial/antifungal finished product produced by the method | OSAKA KASEI CO., LTD. (JP) | 2020-02-18 | — | — | US | claimed |
| US-6238550-B1 | HYDROREFINING CATALYST | EXXON RESEARCH AND ENGINEERING COMPANY | 2001-05-29 | — | — | US | claimed |
| WO-2001036328-A1 | METHOD FOR THE SYNTHESIS OF MOLECULAR SIEVES | EXXON CHEMICAL PATENTS INC. (US) | 2001-05-25 | — | — | WO | claimed |
| US-6025404-A | FROTHING A LATEX THAT CONTAINS A DISPERSED POLYMER HAVING PENDANT CATIONIC GROUPS OR ADSORBING CATIONIC MOLECULES OR BOTH, AND PENDANT ACID GROUPS; AND B) RENDERING THE FROTHED LATEX SUFFICIENTLY BASIC TO MAKE THE CELLULAR ARTICLE. | THE DOW CHEMICAL COMPANY (US) | 2000-02-15 | — | — | US | claimed |
| EP-0477198-B1 | METHOD FOR RECOVERING RECOMBINANT PROTEINS | PITMAN MOORE INC (US) | 1993-11-03 | — | — | EP | claimed |
| US-5254273-A | Lubricating oil and intercalation compound of metal phosphorus chalcoenide and alkylamine or alkylammonium chloride | KYODO YUSHI CO., LTD. (JP) | 1993-10-19 | — | — | US | claimed |
| EP-0477198-A1 | METHOD FOR RECOVERING RECOMBINANT PROTEINS. | PITMAN MOORE INC (US) | 1992-04-01 | — | — | EP | claimed |
| US-5101018-A | Somatotropin, Amine Salt or Quaternary Ammonium Salt | INTERNATIONAL MINERALS & CHEMICAL CORP. (US) | 1992-03-31 | — | — | US | claimed |
| WO-1991013122-A1 | SUBSTITUTED XANTHENE COMPOUNDS | STEADFAST, INCORPORATED (US) | 1991-09-05 | — | — | WO | claimed |
| WO-1990015876-A1 | METHOD FOR RECOVERING RECOMBINANT PROTEINS | PITMAN-MOORE, INC. (US) | 1990-12-27 | — | — | WO | claimed |
| US-3997705-A | Method of coagulating a fluoro-elastomer from an aqueous dispersion thereof | DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) | 1976-12-14 | — | — | US | claimed |