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 6)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC6A3 known ✓ | Q01959 | 1/20 | 0.36 |
| ▸ | SLC6A4 known ✓ | P31645 | 3/20 | 0.36 |
| ▸ | HTR2A known ✓ | P28223 | 2/20 | 0.35 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.31 |
| ▸ | KEAP1 | Q14145 | 1/20 | 0.31 |
| ▸ | PNMT | P11086 | 1/20 | 0.30 |
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 SCHEMBL27452976 | 1.00 | SLC6A3 (0.36) | SLC6A3SLC6A4HTR2AALDH1A1KEAP1 | |
| SCHEMBL6220505 | 0.98 | SLC6A3 (0.37) | SLC6A3SLC6A4HTR2AALDH1A1KEAP1 | |
| SCHEMBL3017956 | 0.98 | SLC6A3 (0.37) | SLC6A3SLC6A4HTR2AALDH1A1KEAP1 | |
| SCHEMBL13692462 | 0.79 | PNMT (0.44) | SLC6A3SLC6A4PNMT | |
| SCHEMBL3060436 | 0.79 | PNMT (0.44) | SLC6A3SLC6A4PNMT | |
| SCHEMBL6640956 | 0.79 | PNMT (0.44) | SLC6A3SLC6A4PNMT | |
| SCHEMBL3017954 | 0.76 | SLC6A3 (0.37) | SLC6A3ALDH1A1 | |
| SCHEMBL22863972 | 0.75 | SLC6A3 (0.41) | SLC6A3ALDH1A1KEAP1PNMT | |
| SCHEMBL13211949 | 0.74 | ALDH1A1 (0.43) | SLC6A3SLC6A4ALDH1A1 | |
| SCHEMBL7812782 | 0.72 | SLC6A4 (0.34) | SLC6A4HTR2A |
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 10 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-1122667-C | Process for preparing N6-substituted deaza-adenosine derivatives | AVENTIS PHARM PROD INC (US) | 2003-10-01 | — | — | CN | claimed |
| CN-1333773-A | Process for preparing N6-substituted deaza-adenosine derivatives | AVENTIS PHARM PROD INC (US) | 2002-01-30 | — | — | CN | claimed |
| US-20040127434-A1 | Novel adenosine analogues and their use as pharmaceutical agents | SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) | 2004-07-01 | — | — | US | disclosed |
| CN-1122667-C | Process for preparing N6-substituted deaza-adenosine derivatives | AVENTIS PHARM PROD INC (US) | 2003-10-01 | — | — | CN | disclosed |
| CN-1112354-C | Stereoselective preparation of chiral 1-aryl-and 1-heteroaryl-2-substituted ethyl-2-amines | AVENTIS PHARMACEUTICAL CO (US) | 2003-06-25 | — | — | CN | disclosed |
| EP-1175420-B1 | PROCESS FOR PREPARING N6-SUBSTITUTED DEAZA-ADENOSINE DERIVATIVES | AVENTIS PHARMA INC (US) | 2003-03-26 | — | — | EP | disclosed |
| CN-1388119-A | Stereoselective preparation of chiral 1-aryl-and 1-heteroaryl-2-substituted ethyl-2-amines | AVENTIES PHARMACEUTICALS INC (US) | 2003-01-01 | — | — | CN | disclosed |
| CN-1333773-A | Process for preparing N6-substituted deaza-adenosine derivatives | AVENTIS PHARM PROD INC (US) | 2002-01-30 | — | — | CN | disclosed |
| US-6184382-B1 | 4-(7-((1-((3-CHLOROTHIEN-2-YL)METHYL)PROPYL)AMINO)-3H-IMIDAZO (4, 5-B)PYRID-3-YL) N-ETHYL-2,3-DIHYDROXYCYCLOPENTANECARBOXAMIDE ARE USEFUL AS CARDIOVASCULAR AGENTS, ANTIHYPERTENSIVE, ANTI-ISCHEMIC AGENTS, | AVENTIS PHARMACEUTICALS PRODUCTS INC. | 2001-02-06 | — | — | US | disclosed |
| CN-1230176-A | Stereoselective preparation of chiral 1-aryl-and 1-heteroaryl-2-substituted ethyl-2-amines | RHONE POULENC RORER PHARMA (US) | 1999-09-29 | — | — | CN | disclosed |
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-20040127434-A1 | Novel adenosine analogues and their use as pharmaceutical agents | ADORA1, ADORA2A, ADORA2B | SLC6A3 2716/4885SLC6A4 2280/4885HTR2A 512/4885 |
“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.