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 | |
|---|---|---|---|---|
| ▸ | ESR1 known ✓ | P03372 | 1/20 | 0.44 |
| ▸ | ESR2 known ✓ | Q92731 | 1/20 | 0.44 |
| ▸ | NR3C1 known ✓ | P04150 | 2/20 | 0.36 |
| ▸ | SLC6A2 known ✓ | P23975 | 1/20 | 0.33 |
| ▸ | SLC6A4 known ✓ | P31645 | 1/20 | 0.33 |
| ▸ | SLC6A3 known ✓ | Q01959 | 1/20 | 0.33 |
| ▸ | KMT2A | Q03164 | 3/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.36 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.36 |
| ▸ | HTT | P42858 | 1/20 | 0.36 |
| ▸ | TSHR | P16473 | 2/20 | 0.35 |
| ▸ | MAPT | P10636 | 1/20 | 0.35 |
| ▸ | TAS2R14 | Q9NYV8 | 1/20 | 0.33 |
| ▸ | TRPM8 | Q7Z2W7 | 1/20 | 0.33 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.33 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.33 |
| ▸ | MEN1 | O00255 | 1/20 | 0.33 |
| ▸ | NPC1 | O15118 | 1/20 | 0.33 |
| ▸ | RAB9A | P51151 | 1/20 | 0.33 |
| ▸ | AOC3 | Q16853 | 1/20 | 0.33 |
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 SCHEMBL3922809 | 0.80 | ALDH1A1 (0.46) | ALDH1A1TSHRCYP2C19AOC3 | |
| SCHEMBL266738 | 0.78 | ALDH1A1 (0.48) | ALDH1A1TSHRCYP2C19AOC3SLC6A2 | |
| Hydrochloric Acid SCHEMBL9147171 | 0.73 | TSHR (0.47) | ALDH1A1TSHRCYP2C19MAPK1AOC3 | |
| Hydrochloric Acid SCHEMBL859872 | 0.72 | ESR1 (0.50) | ESR1ESR2ALDH1A1HTTMAPT | |
| SCHEMBL2038161 | 0.72 | ESR1 (0.72) | ESR1ESR2KMT2AALDH1A1ALOX12 | |
| Hydrochloric Acid SCHEMBL11126993 | 0.71 | KCNH2 (0.48) | KMT2AMAPT | |
| SCHEMBL22016404 | 0.71 | TAS2R14 (0.42) | NR3C1KMT2AALDH1A1TSHRMAPT | |
| SCHEMBL8415458 | 0.71 | TSHR (0.48) | ALDH1A1TSHRCYP2C19MAPK1AOC3 | |
| Hydrochloric Acid SCHEMBL28173092 | 0.71 | CALM1 (0.44) | KMT2ATSHRMAPTCYP2C19MEN1 | |
| SCHEMBL1276090 | 0.70 | CALM1 (0.48) | ESR1ESR2KMT2ATSHRCYP2C19 |
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 19 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4394016-B1 | CHEMILUMINESCENT SUBSTRATE SOLUTION, CHEMILUMINESCENCE ENHANCER AND USE THEREOF | SHENZHEN MINDRAY BIOMEDICAL ELECTRONICS CO LTD (CN) | 2025-08-20 | — | — | EP | disclosed |
| EP-4394016-A1 | CHEMILUMINESCENT SUBSTRATE SOLUTION, CHEMILUMINESCENCE ENHANCER AND USE THEREOF | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (CN) | 2024-07-03 | — | — | EP | disclosed |
| CN-113717714-A | Chemiluminescence reinforcing agent, preparation method thereof and application thereof in chemiluminescence liquid | 大连博格林生物科技有限公司 | 2021-11-30 | — | — | CN | disclosed |
| US-20160033497-A1 | Luminescence methods and reagents for analyte detection | WANG TIANXIN (US) | 2016-02-04 | — | — | US | disclosed |
| US-20150323541-A1 | METHODS AND REAGENTS FOR ANALYTE DETECTION | ORANGENE INC. (US) | 2015-11-12 | — | — | US | disclosed |
| US-20110097723-A1 | Methods and reagents for analyte detection | ORANGENE INC. | 2011-04-28 | — | — | US | disclosed |
| US-6022964-A | SPIROADAMANTYL DIOXETANES WITH AN ALKOXY SUBSTITUENT AND A NAPHTHYL SUBSTITUENT ON THE DIOXETANE RING WHICH CAN BE ACTIVATED BY ENZYMATIC CLEAVAGE OF LABILE GROUP; KINETICS AND SIGNAL INTENSITY DEPENDS ON ELECTRON-ACTIVATING GROUP | TROPIX, INC. (US) | 2000-02-08 | — | — | US | disclosed |
| EP-0649417-A1 | IMPROVED CHEMILUMINESCENT 1,2-DIOXETANES | TROPIX, INC. (US) | 1995-04-26 | — | — | EP | disclosed |
| EP-0649417-A4 | IMPROVED CHEMILUMINESCENT 1,2-DIOXETANES. | TROPIX INC (US) | 1995-02-27 | — | — | EP | disclosed |
| WO-1994026726-A1 | IMPROVED CHEMILUMINESCENT 1,2-DIOXETANES | TROPIX, INC. (US) | 1994-11-24 | — | — | WO | disclosed |
| EP-0009411-B2 | PHOTOGRAPHIC RECORDING MATERIAL CONTAINING POLYMERS WHICH COORDINATE WITH METAL IONS | EASTMAN KODAK COMPANY (a New Jersey corporation) (US) | 1986-11-26 | — | — | EP | disclosed |
| EP-0056664-B1 | ADDITION POLYMERS AND METAL COMPLEXES THEREOF | EASTMAN KODAK COMPANY (a New Jersey corporation) (US) | 1986-11-12 | — | — | EP | disclosed |
| US-4454060-A | Liquid detergent composition with a cationic foam stabilizing copolymer containing pendant quaternary nitrogen groups and pendant hydrophobic groups | COLGATE-PALMOLIVE COMPANY (US) | 1984-06-12 | — | — | US | disclosed |
| EP-0009411-B1 | PHOTOGRAPHIC RECORDING MATERIAL CONTAINING POLYMERS WHICH COORDINATE WITH METAL IONS | EASTMAN KODAK COMPANY (a New Jersey corporation) (US) | 1983-06-01 | — | — | EP | disclosed |
| EP-0056664-A2 | Addition polymers and metal complexes thereof | EASTMAN KODAK COMPANY (a New Jersey corporation) (US) | 1982-07-28 | — | — | EP | disclosed |
| US-4228257-A | Polymers for use in image receiving elements for metallizable dyes in image transfer film units | EASTMAN KODAK COMPANY (US) | 1980-10-14 | — | — | US | disclosed |
| EP-0009411-A2 | Photographic recording material containing polymers which coordinate with metal ions | EASTMAN KODAK COMPANY (a New Jersey corporation) (US) | 1980-04-02 | — | — | EP | disclosed |
| US-4193796-A | CONTAINING AMIDE OR ANIONIC SULFONATE UNITA AND IMINODIACETIC ACID UNITS; USED AS OR WITH MORDANT | EASTMAN KODAK COMPANY (US) | 1980-03-18 | — | — | US | disclosed |
| US-4080346-A | DIFFUSION TRANSFER IMAGE DYE MORDANTS | POLAROID CORPORATION (US) | 1978-03-21 | — | — | US | disclosed |