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 1)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CTSD | P07339 | 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 SCHEMBL3667602 | 1.00 | CTSD (0.33) | CTSD | |
| Hydrochloric Acid SCHEMBL812503 | 1.00 | CTSD (0.33) | CTSD | |
| Ethane SCHEMBL9190139 | 0.97 | CTSD (0.32) | CTSD | |
| Methane SCHEMBL9190165 | 0.97 | CTSD (0.32) | CTSD | |
| SCHEMBL140407 | 0.97 | CTSD (0.35) | CTSD | |
| Methyl Alcohol SCHEMBL9190282 | 0.95 | CTSD (0.31) | CTSD | |
| Bromide SCHEMBL27948710 | 0.94 | CTSD (0.33) | CTSD | |
| Fluoride SCHEMBL27933141 | 0.94 | CTSD (0.33) | CTSD | |
| Iodide SCHEMBL27933185 | 0.94 | CTSD (0.33) | CTSD | |
| Bromide SCHEMBL1539651 | 0.94 | CTSD (0.33) | CTSD |
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 1098 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119462777-A | Preparation method of pentamethyl cyclopentadienyl titanium trichloride | 中船(邯郸)派瑞特种气体股份有限公司 | 2025-02-18 | — | — | CN | claimed |
| CN-118307592-A | Quaternary phosphate compound and preparation method thereof | 北京大学 | 2024-07-09 | — | — | CN | claimed |
| WO-2024078525-A1 | PHOSPHINE-PHENOL HALF-METALLOCENE COMPLEX, AND PREPARATION METHOD THEREFOR AND USE THEREOF | 中国石油化工股份有限公司 | 2024-04-18 | — | — | WO | claimed |
| CN-115966668-A | Silicon-carbon composite material and preparation method and application thereof | 胜华新材料科技(眉山)有限公司 | 2023-04-14 | — | — | CN | claimed |
| CN-115521529-A | Composite material for preparing test tube cover and preparation method thereof | 深圳市远景医疗器械模具有限公司 | 2022-12-27 | — | — | CN | claimed |
| CN-112645971-B | Method for directly preparing alkyl borate compound from alkyl halide | 中国科学院兰州化学物理研究所 | 2021-12-24 | — | — | CN | claimed |
| CN-112645971-A | Method for directly preparing alkyl borate compound from alkyl halide | 中国科学院兰州化学物理研究所 | 2021-04-13 | — | — | CN | claimed |
| US-20190091657-A1 | HYBRID MATERIAL FOR CHROMATOGRAPHIC SEPARATIONS COMPRISING A SUPERFICIALLY POROUS CORE AND A SURROUNDING MATERIAL | WATERS TECHNOLOGIES CORPORATION | 2019-03-28 | — | — | US | claimed |
| US-20190015815-A1 | SUPERFICIALLY POROUS MATERIALS COMPRISING A COATED CORE HAVING NARROW PARTICLE SIZE DISTRIBUTION; PROCESS FOR THE PREPARATION THEREOF; AND USE THEREOF FOR CHROMATOGRAPHIC SEPARATIONS | WATERS TECHNOLOGIES CORPORATION | 2019-01-17 | — | — | US | claimed |
| EP-3426388-A1 | SUPERFICIALLY POROUS MATERIALS COMPRISING A COATED CORE HAVING NARROW PARTICLE SIZE DISTRIBUTION; PROCESS FOR THE PREPARATION THEREOF; AND USE THEREOF FOR CHROMATOGRAPHIC SEPARATIONS | Waters Technologies Corporation (US) | 2019-01-16 | — | — | EP | claimed |
| US-6284700-B1 | COORDINATION POLYMERIZATION CATALYSTS | SAMSUNG GENERAL CHEMICALS CO., LTD. (KR) | 2001-09-04 | — | — | US | claimed |
| US-6281304-B1 | USING A METALLOCENE COMPLEX | BASF AKTIENGESELLSCHAFT (DE) | 2001-08-28 | — | — | US | claimed |
| US-6277934-B1 | A SYNDIOTACTIC HOMO- OR COPOLYMER FROM A STYRENIC COMPOUND IN THE PRESENCE OF A METALLOCENE OF HIGH, STABLE ACTIVITY COMPRISING A TITANIUM COMPOUND AND AN ORGANIC ALUMINOXY COMPOUND OF SPECIFIC NUCLEAR MAGNETIC RESONANCE SPECTRUM | IDEMITSU PETROCHEMICAL CO., LTD. (JP) | 2001-08-21 | — | — | US | claimed |
| EP-1104774-A1 | Method for selective hydrogenation of polymer containing conjugated diene | Korea Kumho Petrochemical Co. Ltd. (KR) | 2001-06-06 | — | — | EP | claimed |
| US-6013744-A | ADDING A MONO- OR DIHYDROCARBYLSILANE ADJUVANT TO THE MONOMER MIXTURE AND CONTACTING UNDER POLYMERIZATION CONDITIONS WITH A GROUP 4 METAL COMPLEX OF GIVEN FORMULA AND ACTIVATING COCATALYST | THE DOW CHEMICAL COMPANY (US) | 2000-01-11 | — | — | US | claimed |
| EP-0964004-A1 | New metallocene catalyst for olefin or styrene polymerization and polymerization method using the metallocene catalyst | Samsung General Chemicals Co., Ltd. (KR) | 1999-12-15 | — | — | EP | claimed |
| EP-0420134-B1 | Process for producing styrene polymers | IDEMITSU KOSAN CO (JP) | 1996-02-07 | — | — | EP | claimed |
| US-5340892-A | Addition polymerization in presence of a polymerization catalysts mixture consisting of a cyclopentadienyl titanium compound and an alkylaluminoxane to provide a wide molecular weight distribution | IDEMITSU KOSAN CO., LTD. (JP) | 1994-08-23 | — | — | US | claimed |
| US-5023304-A | Using coordination catalyst; highly syndiotactic | IDEMITSU KOSAN CO., LTD. (JP) | 1991-06-11 | — | — | US | claimed |
| EP-0420134-A2 | Process for producing styrene polymers | IDEMITSU KOSAN COMPANY LIMITED (JP) | 1991-04-03 | — | — | EP | claimed |