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 SCHEMBL28412591 | 1.00 | — | — | |
| SCHEMBL1412044 | 0.96 | — | — | |
| Bromide SCHEMBL11751081 | 0.93 | — | — | |
| SCHEMBL28102401 | 0.93 | — | — | |
| Ammonia Solution, Strong SCHEMBL3496168 | 0.93 | — | — | |
| Water SCHEMBL5156556 | 0.93 | — | — | |
| SCHEMBL27409539 | 0.93 | — | — | |
| Trimethylammonium SCHEMBL27711366 | 0.84 | — | — | |
| SCHEMBL18766380 | 0.82 | — | — | |
| SCHEMBL1412045 | 0.80 | — | — |
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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118119273-A | ALS-inhibitor herbicide tolerant beet hybrids with enhanced hybrid vigour | 拜耳公司 | 2024-05-31 | — | — | CN | disclosed |
| US-9422244-B2 | Synthesis of substituted pyrazoline carboxamidine derivatives | ABBVIE BAHAMAS LTD. (BS) | 2016-08-23 | — | — | US | disclosed |
| CN-102725272-B | Synthesis of substituted pyrazoline carboxamidine derivatives | ABBOTT HEALTHCARE PRODUCTS BV | 2015-07-15 | — | — | CN | disclosed |
| EP-2528900-B1 | SYNTHESIS OF SUBSTITUTED PYRAZOLINE CARBOXAMIDINE DERIVATIVES | ABBVIE BAHAMAS LTD (BS) | 2014-06-11 | — | — | EP | disclosed |
| US-20130060041-A1 | SYNTHESIS OF SUBSTITUTED PYRAZOLINE CARBOXAMIDINE DERIVATIVES | ABBOTT HOSPITALS LIMITED (BS) | 2013-03-07 | — | — | US | disclosed |
| CN-102725272-A | Synthesis of substituted pyrazoline carboxamidine derivatives | ABBOTT HEALTHCARE PRODUCTS BV | 2012-10-10 | — | — | CN | disclosed |
| EP-0234176-B2 | Pyrazoline compounds | CIBA GEIGY AG (CH) | 1996-05-22 | — | — | EP | disclosed |
| US-RE35198-E | Image forming member for electrophotography | CANON KABUSHIKI KAISHA (JP) | 1996-04-02 | — | — | US | disclosed |
| US-5308545-A | Pyrazoline compounds | CIBA-GEIGY CORPORATION (US) | 1994-05-03 | — | — | US | disclosed |
| US-4877709-A | Image forming member for electrophotography | CANON KABUSHIKI KAISHA (JP) | 1989-10-31 | — | — | US | disclosed |
| US-4557990-A | Hydrogenated amorphous silicon photosensitive member for electrophotography | CANON KABUSHIKI KAISHA (JP) | 1985-12-10 | — | — | US | disclosed |
| US-4551405-A | Image forming process employing member with a depletion layer | CANON KABUSHIKI KAISHA (JP) | 1985-11-05 | — | — | US | disclosed |
| US-4461819-A | HYDROGENATED AMORPHOUS SILICON CHARGE GENERATION LAYER | CANON KABUSHIKI KAISHA (JP) | 1984-07-24 | — | — | US | disclosed |
| EP-0048373-B1 | PROCESS FOR PREPARING PYRAZOLE | BAYER AG (DE) | 1984-05-09 | — | — | EP | disclosed |
| US-4434292-A | Process for the preparation of pyrazole | BAYER AKTIENGESELLSCHAFT (DE) | 1984-02-28 | — | — | US | disclosed |
| EP-0048373-A2 | Process for preparing pyrazole | BAYER AG (DE) | 1982-03-31 | — | — | EP | disclosed |
| US-4322541-A | HYPOTENSIVE AGENTS | E. R. SQUIBB & SONS, INC. (US) | 1982-03-30 | — | — | US | disclosed |
| US-4266065-A | HYPOTENSIVE ACTIVITY | E. R. SQUIBB & SONS, INC. (US) | 1981-05-05 | — | — | US | disclosed |
| US-4003732-A | Pyrazolinium compounds as herbicides | AMERICAN CYANAMID COMPANY (US) | 1977-01-18 | — | — | US | disclosed |
| US-3947583-A | Method for controlling fungi utilizing pyrazolinium compounds | AMERICAN CYANAMID COMPANY (US) | 1976-03-30 | — | — | US | disclosed |