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 14)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | S1PR1 known ✓ | P21453 | 2/20 | 0.36 |
| ▸ | S1PR4 known ✓ | O95977 | 1/20 | 0.33 |
| ▸ | S1PR3 known ✓ | Q99500 | 1/20 | 0.33 |
| ▸ | S1PR5 known ✓ | Q9H228 | 1/20 | 0.33 |
| ▸ | FDPS | P14324 | 3/20 | 0.44 |
| ▸ | DNM1 | Q05193 | 6/20 | 0.38 |
| ▸ | TSHR | P16473 | 2/20 | 0.38 |
| ▸ | LMNA | P02545 | 1/20 | 0.38 |
| ▸ | SMPD1 | P17405 | 2/20 | 0.36 |
| ▸ | THRB | P10828 | 1/20 | 0.35 |
| ▸ | TNNC1 | P63316 | 5/20 | 0.33 |
| ▸ | SGPL1 | O95470 | 1/20 | 0.33 |
| ▸ | GPR183 | P32249 | 1/20 | 0.33 |
| ▸ | CERS2 | Q96G23 | 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 | |
|---|---|---|---|---|
| SCHEMBL93609 | 0.97 | FDPS (0.46) | FDPSDNM1TSHRLMNAS1PR1 | |
| Hydrochloric Acid SCHEMBL9784204 | 0.94 | FDPS (0.41) | FDPSDNM1TSHRLMNAS1PR1 | |
| Hydrochloric Acid SCHEMBL1820523 | 0.94 | FDPS (0.41) | FDPSDNM1TSHRLMNAS1PR1 | |
| Hydrochloric Acid SCHEMBL5084825 | 0.94 | FDPS (0.44) | FDPSDNM1TSHRS1PR1SMPD1 | |
| Methyl Alcohol SCHEMBL22190212 | 0.94 | FDPS (0.46) | FDPSDNM1TSHRLMNAS1PR1 | |
| Hydrochloric Acid SCHEMBL11836901 | 0.94 | FDPS (0.44) | FDPSDNM1TSHRS1PR1SMPD1 | |
| Fluoride SCHEMBL4871826 | 0.93 | FDPS (0.44) | FDPSDNM1TSHRLMNAS1PR1 | |
| Bromide SCHEMBL309594 | 0.93 | FDPS (0.44) | FDPSDNM1TSHRLMNAS1PR1 | |
| Iodide SCHEMBL553007 | 0.93 | FDPS (0.44) | FDPSDNM1TSHRLMNAS1PR1 | |
| Water SCHEMBL661747 | 0.93 | FDPS (0.44) | FDPSDNM1TSHRLMNAS1PR1 |
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 1032 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4735622-A1 | PROTECTING FULLY FUNCTIONAL NUCLEOTIDES FROM DEGRADATION | Illumina, Inc. (US) | 2026-05-06 | — | — | EP | claimed |
| US-20260015560-A1 | COMPOSITIONS FOR POST-CMP CLEANING OF MICROELECTRONIC DEVICES | ENTEGRIS INC (US) | 2026-01-15 | — | — | US | claimed |
| EP-4536612-A1 | COMPOSITION COMPRISING A EUTECTIC MIXTURE COMPRISING AN ALKYLTHIOPHOSPHORIC TRIAMIDE UREASE INHIBITOR | SPECIALTY OPERATIONS FRANCE (FR) | 2025-04-16 | — | — | EP | claimed |
| CN-116178587-B | Quaternary ammonium glycogen, composite antibacterial hydrogel and preparation method and application thereof | 江南大学 | 2025-04-11 | — | — | CN | claimed |
| WO-2025003459-A1 | PROTECTING FULLY FUNCTIONAL NUCLEOTIDES FROM DEGRADATION | ILLUMINA, INC. (US) | 2025-01-02 | — | — | WO | claimed |
| CN-119144153-A | Flame-retardant antistatic polyamide and preparation method thereof | 中化学科学技术研究有限公司 | 2024-12-17 | — | — | CN | claimed |
| CN-117039207-B | Battery, iodine electrode material and preparation method of electrolyte | 广东工业大学 | 2024-07-30 | — | — | CN | claimed |
| CN-118239909-A | Ketone-containing bisfuranyl monomer compound, preparation method thereof, electronic packaging adhesive and application thereof | 中国科学技术大学 | 2024-06-25 | — | — | CN | claimed |
| WO-2024081696-A2 | COMPOSITIONS CONTAINING PHASE CHANGE MATERIALS, METHODS FOR FORMING OBJECTS USING THE SAME, AND METHOD FOR USING THE SAME | PHASE CHANGE ENERGY SOLUTIONS, INC. (US) | 2024-04-18 | — | — | WO | claimed |
| EP-3704086-B1 | PROCESS FOR PREPARING 4-CHLOROBENZYL PROPARGYL ETHER | BASF SE (DE) | 2024-02-21 | — | — | EP | claimed |
| US-5420274-A | Process for the preparation of 2,4-di(alkylamino)-6-alkylthio-s-triazines | CIBA-GEIGY CORPORATION (US) | 1995-05-30 | — | — | US | claimed |
| EP-0648755-A1 | Improved process for the preparation of 2,4-Di(alkylamino)-6-alkylthio-s-triazines | CIBA-GEIGY AG (CH) | 1995-04-19 | — | — | EP | claimed |
| EP-0315906-B1 | PROCESS FOR THE PREPARATION OF ORTHO-NITROPHENETOLE | HOECHST AKTIENGESELLSCHAFT (DE) | 1993-09-08 | — | — | EP | claimed |
| US-4954657-A | Process for the preparation of o-nitrophenetole | HOECHST AKTIENGESELLSCHAFT (DE) | 1990-09-04 | — | — | US | claimed |
| EP-0171762-B1 | PROCESS FOR PREPARING CARBOXYLATE ESTERS | AIR PRODUCTS AND CHEMICALS, INC. (US) | 1990-07-18 | — | — | EP | claimed |
| US-4847405-A | AMINATION, PHASE TRANSFER AGENT | AMERICAN CYANAMID COMPANY (US) | 1989-07-11 | — | — | US | claimed |
| EP-0263205-A1 | Processes for the preparation of compounds comprising substituted phenyl rings | THE UPJOHN COMPANY (US) | 1988-04-13 | — | — | EP | claimed |
| EP-0231257-A1 | CHEMICAL COMPOUNDS COMRPISING SUBSTITUTED PHENYLRINGS | THE UPJOHN COMPANY (US) | 1987-08-12 | — | — | EP | claimed |
| WO-1987000519-A1 | CHEMICAL COMPOUNDS COMRPISING SUBSTITUTED PHENYLRINGS | THE UPJOHN COMPANY (US) | 1987-01-29 | — | — | WO | claimed |
| EP-0171762-A2 | Process for preparing carboxylate esters | AIR PRODUCTS AND CHEMICALS, INC. (US) | 1986-02-19 | — | — | EP | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20260015560-A1 | COMPOSITIONS FOR POST-CMP CLEANING OF MICROELECTRONIC DEVICES | TET2, ASIC1, PIEZO1 | S1PR1 702/4885S1PR4 1065/4885S1PR3 1349/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.