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 SCHEMBL5469303 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL135828 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL4441521 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL28239268 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL23295133 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL6063968 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL249448 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL930844 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL11016935 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL225121 | 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
Appears in 2003 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116813686-B | Asymmetric synthesis method and application of 7-oxo-resorcinol lactone | 欣凯医药化工中间体（上海）有限公司 | 2026-05-15 | — | — | CN | claimed |
| US-20250320221-A1 | NOVEL INTERMEDIATE, METHOD FOR PREPARING THE SAME AND APPLICATION THEREOF | UNIV SICHUAN (CN) | 2025-10-16 | — | — | US | claimed |
| CN-120189948-A | Method for solid phase synthesis of nickel phyllosilicate catalyst under solvent-free condition | 山东科技大学 | 2025-06-24 | — | — | CN | claimed |
| CN-116851038-B | Magnetic nano diacid catalyst and preparation method and catalytic application thereof | 河北师范大学 | 2025-06-13 | — | — | CN | claimed |
| CN-120081738-A | Preparation method of 2, 6-naphthalene dicarboxylic acid and esterified derivative thereof | 东华大学 | 2025-06-03 | — | — | CN | claimed |
| CN-120081474-A | Double-component composite flocculant and preparation method, using method and application thereof | 中国海洋石油集团有限公司 | 2025-06-03 | — | — | CN | claimed |
| US-20250171493-A1 | PROCESSES FOR SYNTHESIS OF WITHANOLIDES AND WITHAFERINS AND ANALOGS THEREOF | H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. | 2025-05-29 | — | — | US | claimed |
| CN-120039825-A | Magnesium-based composite solid hydrogen storage material, hydrogen fuel cell system and hydrogen energy electric bicycle | 江苏兴邦能源科技有限公司 | 2025-05-27 | — | — | CN | claimed |
| CN-120015867-A | Corrosion-resistant candle dust/MXene functional coating and preparation method and application thereof | 上海电力大学 | 2025-05-16 | — | — | CN | claimed |
| CN-119954609-A | 2-Iodo-3, 4,5,6-d4Process for the preparation of phenol | 广州瑞安博医药科技有限公司 | 2025-05-09 | — | — | CN | claimed |
| EP-0650489-A1 | RAPAMYCIN DERIVATIVES | SMITHKLINE BEECHAM CORPORATION (US) | 1995-05-03 | — | — | EP | claimed |
| EP-0234737-B1 | Preparation of piperidinylcyclopentylheptenoic acid derivatives | GLAXO GROUP LTD (GB) | 1994-07-27 | — | — | EP | claimed |
| WO-1994014789-A1 | COUMARIN DERIVATIVES AS RETROVIRAL INHIBITORS | SMITHKLINE BEECHAM CORPORATION (US) | 1994-07-07 | — | — | WO | claimed |
| WO-1994002485-A1 | RAPAMYCIN DERIVATIVES | SMITHKLINE BEECHAM CORPORATION (US) | 1994-02-03 | — | — | WO | claimed |
| EP-0462588-A2 | Olefin block copolymer and method of producing same | MITSUBISHI PETROCHEMICAL CO., LTD. (JP) | 1991-12-27 | — | — | EP | claimed |
| US-4851514-A | ANGIOTENSIN CONVERTING ENZYME INHIBITOR, REACTING CERIUM TRICHLORIDE WITH PHENYLLITHIUM TO PRODUCE TRIPHENYL CERIUM | E. R. SQUIBB & SONS, INC. (US) | 1989-07-25 | — | — | US | claimed |
| US-4835278-A | Preparation of piperidinylcyclopentylheptenoic acid derivatives | GLAXO GROUP LIMITED (GB) | 1989-05-30 | — | — | US | claimed |
| EP-0234737-A1 | Preparation of piperidinylcyclopentylheptenoic acid derivatives | GLAXO GROUP LIMITED (GB) | 1987-09-02 | — | — | EP | claimed |
| US-4590216-A | SYNTHESIS GAS | UNION CARBIDE CORPORATION (US) | 1986-05-20 | — | — | US | claimed |
| US-4524195-A | HALOGENATED HALIDE RARE METALS DISSOLVED WITH ORGANOPHOSPHATE OR ORGANOPHOSPHORAMIDE, REACTED WITH HALOGEN COMPOUND OF TRANSITION METAL | PHILLIPS PETROLEUM COMPANY (US) | 1985-06-18 | — | — | US | claimed |