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 | |
|---|---|---|---|---|
| ▸ | DRD2 known ✓ | P14416 | 14/20 | 0.70 |
| ▸ | DRD3 known ✓ | P35462 | 13/20 | 0.70 |
| ▸ | HTR1A known ✓ | P08908 | 3/20 | 0.70 |
| ▸ | DRD4 known ✓ | P21917 | 3/20 | 0.70 |
| ▸ | HTR2A known ✓ | P28223 | 3/20 | 0.70 |
| ▸ | HTR2C known ✓ | P28335 | 3/20 | 0.70 |
| ▸ | ADRA2A known ✓ | P08913 | 2/20 | 0.70 |
| ▸ | HTR7 known ✓ | P34969 | 2/20 | 0.70 |
| ▸ | ADRA1A known ✓ | P35348 | 2/20 | 0.70 |
| ▸ | HRH1 known ✓ | P35367 | 2/20 | 0.70 |
| ▸ | CHRM4 known ✓ | P08173 | 1/20 | 0.70 |
| ▸ | ADRB1 known ✓ | P08588 | 1/20 | 0.70 |
| ▸ | CHRM5 known ✓ | P08912 | 1/20 | 0.70 |
| ▸ | ADRA2B known ✓ | P18089 | 1/20 | 0.70 |
| ▸ | ADRA2C known ✓ | P18825 | 1/20 | 0.70 |
| ▸ | ADRA1D known ✓ | P25100 | 1/20 | 0.70 |
| ▸ | HTR1D known ✓ | P28221 | 1/20 | 0.70 |
| ▸ | HTR1B known ✓ | P28222 | 1/20 | 0.70 |
| ▸ | SLC6A4 known ✓ | P31645 | 1/20 | 0.70 |
| ▸ | ADRA1B known ✓ | P35368 | 1/20 | 0.70 |
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 SCHEMBL1774393 | 1.00 | DRD2 (0.70) | DRD2DRD3HTR1ADRD4HTR2A | |
| SCHEMBL184341 | 0.99 | DRD2 (0.71) | DRD2DRD3HTR1ADRD4HTR2A | |
| Bromide SCHEMBL1775020 | 0.98 | DRD2 (0.69) | DRD2DRD3HTR1ADRD4HTR2A | |
| SCHEMBL1774667 | 0.95 | DRD2 (0.66) | DRD2DRD3HTR1ADRD4HTR2A | |
| Maleic Acid SCHEMBL1774461 | 0.94 | DRD2 (0.64) | DRD2DRD3HTR1ADRD4HTR2A | |
| Hydrochloric Acid SCHEMBL22228320 | 0.91 | DRD2 (0.72) | DRD2DRD3HTR1ADRD4HTR2A | |
| Hydrochloric Acid SCHEMBL22228318 | 0.91 | DRD2 (0.72) | DRD2DRD3HTR1ADRD4HTR2A | |
| SCHEMBL3674514 | 0.90 | DRD2 (0.71) | DRD2DRD3HTR1ADRD4HTR2A | |
| SCHEMBL18041270 | 0.90 | DRD2 (0.71) | DRD2DRD3HTR1ADRD4HTR2A | |
| Bromide SCHEMBL1774914 | 0.89 | DRD2 (0.70) | DRD2DRD3HTR1ADRD4HTR2A |
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 74 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2925324-B1 | TRANS-4-{2-[4-(2,3-DICHLOROPHENYL)-PIPERAZIN-1-YL]-ETHYL}-N,N-DIMETHYLCARBAMOYL-CYCLOHEXYLAMINE FOR TREATING PRIMARY NEGATIVE SYMPTOMS OF SCHIZOPHRENIA | RICHTER GEDEON NYRT (HU) | 2020-12-30 | — | — | EP | claimed |
| EP-3653211-A1 | TRANS-4-{2-[4-(2,3-DICHLOROPHENYL)-PIPERAZIN-1-YL]-ETHYL}-N,N-DIMETHYLCARBAMOYL-CYCLO-HEXYLAMINE FOR TREATING NEGATIVE SYMPTOMS OF SCHIZOPHRENIA | Richter Gedeon Nyrt. (HU) | 2020-05-20 | — | — | EP | claimed |
| EP-2185155-B1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECPTOR LIGANDS | RICHTER GEDEON NYRT (HU) | 2017-10-04 | — | — | EP | claimed |
| EP-2155696-B1 | PIPERAZINE SALTS AS D3/D2 ANTAGONISTS | RICHTER GEDEON NYRT (HU) | 2017-03-22 | — | — | EP | claimed |
| US-20150306094-A1 | TRANS-4--N,N-DIMETHYLCARBAMOYL-CYCLOHEXYLAMINE FOR TREATING NEGATIVE SYMPTOMS OF SCHIZOPHRENIA | RICHTER GEDEON NYRT. (HU) | 2015-10-29 | — | — | US | claimed |
| EP-2925324-A1 | TRANS-4-{2-[4-(2,3-DICHLOROPHENYL)-PIPERAZIN-1-YL]-ETHYL}-N,N-DIMETHYLCARBAMOYL-CYCLOHEXYLAMINE FOR TREATING NEGATIVE SYMPTOMS OF SCHIZOPHRENIA | Richter Gedeon Nyrt. (HU) | 2015-10-07 | — | — | EP | claimed |
| EP-2164572-B2 | CARBAMOYL-CYCLOHEXANES FOR TREATING ACUTE MANIA | RICHTER GEDEON NYRT (HU) | 2015-09-16 | — | — | EP | claimed |
| WO-2014083522-A1 | TRANS-4-{2-[4-(2,3-DICHLOROPHENYL)-PIPERAZIN-1-YL]-ETHYL}-N,N-DIMETHYLCARBAMOYL-CYCLOHEXYLAMINE FOR TREATING NEGATIVE SYMPTOMS OF SCHIZOPHRENIA | RICHTER GEDEON NYRT. (HU) | 2014-06-05 | — | — | WO | claimed |
| EP-2164572-B1 | CARBAMOYL-CYCLOHEXANES FOR TREATING ACUTE MANIA | RICHTER GEDEON NYRT (HU) | 2012-11-14 | — | — | EP | claimed |
| US-20120028991-A1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECEPTOR LIGANDS | FOREST LABORATORIES HOLDINGS LTD. (BM) | 2012-02-02 | — | — | US | claimed |
| EP-2185155-A1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECPTOR LIGANDS | Forest Laboratories Holdings Limited (BM) | 2010-05-19 | — | — | EP | claimed |
| EP-2164572-A2 | CARBAMOYL-CYCLOHEXANES FOR TREATING ACUTE MANIA | Richter Gedeon NYRT (HU) | 2010-03-24 | — | — | EP | claimed |
| EP-2164492-A1 | (THIO) -CARBAMOYL-CYCLOHEXANE DERIVATIVES AND METHOD FOR TREATING SCHIZOPHRENIA | Richter Gedeon NYRT (HU) | 2010-03-24 | — | — | EP | claimed |
| EP-2155696-A2 | PIPERAZINE SALTS AS D3/D2 ANTAGONISTS | Richter Gedeon NYRT (HU) | 2010-02-24 | — | — | EP | claimed |
| WO-2009020897-A1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECPTOR LIGANDS | FOREST LABORATORIES HOLDINGS LIMITED (BM) | 2009-02-12 | — | — | WO | claimed |
| US-20090036468-A1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECEPTOR LIGANDS | FOREST LABORATORIES HOLDINGS LIMITED (BM) | 2009-02-05 | — | — | US | claimed |
| US-20090023750-A1 | NOVEL SALTS OF PIPERAZINE COMPOUNDS AS D3/D2 ANTAGONISTS | RICHTER GEDEON NYRT. (HU) | 2009-01-22 | — | — | US | claimed |
| WO-2008142463-A2 | CARBAMOYL-CYCLOHEXANES FOR TREATING ACUTE MANIA | RICHTER GEDEON NYRT. (HU) | 2008-11-27 | — | — | WO | claimed |
| WO-2008142462-A1 | (THIO) -CARBAMOYL-CYCLOHEXANE DERIVATIVES AND METHOD FOR TREATING SCHIZOPHRENIA | RICHTER GEDEON NYRT. (HU) | 2008-11-27 | — | — | WO | claimed |
| WO-2008139235-A2 | NOVEL PIPERAZINE SALTS AS D3/D2 ANTAGONISTS | RICHTER GEDEON NYRT. (HU) | 2008-11-20 | — | — | WO | 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 (3 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-20120028991-A1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECEPTOR LIGANDS | HTR5A, SLC6A3, HTR1A | DRD2 12/4885DRD3 54/4885HTR1A 3/4885 |
| US-20090036468-A1 | PHARMACEUTICAL COMPOSITIONS CONTAINING DOPAMINE RECEPTOR LIGANDS AND METHODS OF TREATMENT USING DOPAMINE RECEPTOR LIGANDS | HTR5A, SLC6A3, HTR1A | DRD2 12/4885DRD3 54/4885HTR1A 3/4885 |
| US-20090023750-A1 | NOVEL SALTS OF PIPERAZINE COMPOUNDS AS D3/D2 ANTAGONISTS | DRD2, DRD3, DRD4 | DRD2 1/4885DRD3 2/4885HTR1A 130/4885 |
“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.