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 | |
|---|---|---|---|---|
| ▸ | KDR known ✓ | P35968 | 1/20 | 0.55 |
| ▸ | TOP2A known ✓ | P11388 | 2/20 | 0.55 |
| ▸ | TOP2B known ✓ | Q02880 | 2/20 | 0.55 |
| ▸ | PDGFRB known ✓ | P09619 | 1/20 | 0.47 |
| ▸ | PDGFRA known ✓ | P16234 | 1/20 | 0.47 |
| ▸ | MGAM | O43451 | 1/20 | 0.96 |
| ▸ | CFTR | P13569 | 1/20 | 0.59 |
| ▸ | BCAT1 | P54687 | 1/20 | 0.55 |
| ▸ | RAB9A | P51151 | 5/20 | 0.53 |
| ▸ | PSMD14 | O00487 | 1/20 | 0.53 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.50 |
| ▸ | HPGD | P15428 | 1/20 | 0.50 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.50 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.50 |
| ▸ | MAP4K4 | O95819 | 1/20 | 0.49 |
| ▸ | CSNK1G2 | P78368 | 1/20 | 0.49 |
| ▸ | CLK4 | Q9HAZ1 | 1/20 | 0.49 |
| ▸ | MKNK2 | Q9HBH9 | 1/20 | 0.49 |
| ▸ | MAP4K5 | Q9Y4K4 | 1/20 | 0.49 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.48 |
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 SCHEMBL9114407 | 1.00 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| SCHEMBL28048 | 0.98 | MGAM (1.00) | MGAMCFTRKDRTOP2ATOP2B | |
| SCHEMBL29362407 | 0.98 | MGAM (1.00) | MGAMCFTRKDRTOP2ATOP2B | |
| Fluoride SCHEMBL27513846 | 0.96 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| SCHEMBL27611260 | 0.96 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| Fluoride SCHEMBL27790822 | 0.96 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| Water SCHEMBL28182355 | 0.96 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| SCHEMBL27565246 | 0.96 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| Ammonia Solution, Strong SCHEMBL27447121 | 0.96 | MGAM (0.96) | MGAMCFTRKDRTOP2ATOP2B | |
| Formaldehyde SCHEMBL28117649 | 0.95 | MGAM (0.93) | MGAMCFTRKDRTOP2ATOP2B |
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 60 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-3056489-A | — | — | None | — | — | JP | disclosed |
| CN-118515699-A | Hirsutine alkaloid boric acid derivative and preparation method and application thereof | 中国海洋大学 | 2024-08-20 | — | — | CN | disclosed |
| CN-117986254-A | Hirsutine alkaloid derivative, and preparation method and application thereof | 中国海洋大学 | 2024-05-07 | — | — | CN | disclosed |
| CN-111448192-B | Process for preparing anthelmintic 4-amino-quinoline-3-carboxamide derivatives | 拜耳动物保健有限责任公司 | 2024-04-12 | — | — | CN | disclosed |
| CN-110278711-B | Tricyclosulfones as rory modulators | 百时美施贵宝公司 | 2023-12-15 | — | — | CN | disclosed |
| US-20220380736-A1 | METHODS AND COMPOSITIONS FOR KILLING A TARGET BACTERIUM | Locus Biosciences, Inc. | 2022-12-01 | — | — | US | disclosed |
| CN-113975277-A | Therapeutic agent for respiratory infection | 杏林制药株式会社 | 2022-01-28 | — | — | CN | disclosed |
| EP-3630779-A1 | ANTIBIOTIC RESISTANCE BREAKERS | Kings College London (GB) | 2020-04-08 | — | — | EP | disclosed |
| CN-110278711-A | TRICYCLIC SULFONES AS ROR GAMMA MODULATORS | 百时美施贵宝公司 | 2019-09-24 | — | — | CN | disclosed |
| CN-108395413-B | A kind of preparation method of morpholine -3- carboxylic acid | 上海馨远医药科技有限公司 | 2019-05-28 | — | — | CN | disclosed |
| CN-1007977-B | PROCESS FOR THE PREPARATION OF 7-AMINO-1-CYCLOPXOPYL-6, 8-DIHALOGENO-1, 4-DIHYDRO-4-OXO-3-QUINOLINECARBOXYLIC ACIDS | BAYER AG (DE) | 1990-05-16 | — | — | CN | disclosed |
| US-4885295-A | ANALGESICS; ANTIINFLAMMATORY AGENTS; RHEUMATIC DISEASES | STERLING DRUG INC. (US) | 1989-12-05 | — | — | US | disclosed |
| CN-1033055-A | Quinoline carboxylic acid derivative | NIPPON SHINYAKU CO LTD (JP) | 1989-05-24 | — | — | CN | disclosed |
| US-RE32761-E | ANALGESICS, ANTIRHEUMATIC AND ANTIINFLAMMATORY AGENT | STERLING DRUG INC. (US) | 1988-10-04 | — | — | US | disclosed |
| EP-0085392-B1 | SUNLIGHT-ENERGY-STORING SUBSTANCES AND SUNLIGHT-ENERGY-STORING METHOD USING THE SAME | MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) | 1987-01-21 | — | — | EP | disclosed |
| US-4634776-A | ANALGESIC, ANTIRHEUMATIC, ANTIINFLAMMATORY | STERLING DRUG, INC. (US) | 1987-01-06 | — | — | US | disclosed |
| US-4581354-A | ANALGESICS;ANTI-RHEUMATIC AND ANTI-INFLAMMATORY AGENTS | STERLING DRUG INC. (US) | 1986-04-08 | — | — | US | disclosed |
| EP-0171037-A2 | 3-Carbonyl-1-aminoalkyl-1H-indoles useful as analgesics and preparation thereof | STERLING WINTHROP INC. (US) | 1986-02-12 | — | — | EP | disclosed |
| US-4449516-A | Sunlight-energy-storing method | MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) | 1984-05-22 | — | — | US | disclosed |
| EP-0085392-A2 | Sunlight-energy-storing substances and sunlight-energy-storing method using the same | MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) | 1983-08-10 | — | — | EP | disclosed |