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 SCHEMBL5057708 | 1.00 | CA5A (0.50) | — | |
| Sulfuric Acid SCHEMBL27596127 | 0.95 | CA5A (0.60) | — | |
| Hydrochloric Acid SCHEMBL22441990 | 0.95 | — | — | |
| Methane SCHEMBL29041626 | 0.95 | — | — | |
| SCHEMBL5517182 | 0.94 | CA5A (0.56) | — | |
| SCHEMBL82 | 0.94 | — | — | |
| SCHEMBL3128058 | 0.94 | — | — | |
| SCHEMBL4432240 | 0.94 | — | — | |
| SCHEMBL2875981 | 0.89 | — | — | |
| SCHEMBL7212487 | 0.89 | — | — |
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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20230145442-A1 | CONDENSATION PRODUCT FOR USE IN A METHOD FOR THE TREATMENT OF COVID-19 | IFOM FONDAZIONE ISTITUTO FIRC DI ONCOLOGIA MOLECOLARE (IT) | 2023-05-11 | — | — | US | disclosed |
| EP-4125832-A1 | CONDENSATION PRODUCT FOR USE IN A METHOD FOR THE TREATMENT OF COVID-19 | BASF SE (DE) | 2023-02-08 | — | — | EP | disclosed |
| CN-106573047-B | Adjuvant | 莱特弗克斯有限公司 | 2021-10-12 | — | — | CN | disclosed |
| CN-210065171-U | Chlorosulfonic acid production system | 华强化工集团股份有限公司 | 2020-02-14 | — | — | CN | disclosed |
| WO-2019182037-A1 | ANTISENSE OLIGONUCLEOTIDE HAVING REDUCED TOXICITY | 国立大学法人東京工業大学 | 2019-09-26 | — | — | WO | disclosed |
| CN-110085449-A | Print energy accumulating device and its film and the ink for printing film | 印制能源技术有限公司 | 2019-08-02 | — | — | CN | disclosed |
| CN-109336063-A | Between/system and technique of paraphthaloyl chloride End gas production chlorosulfonic acid | 山东凯盛新材料股份有限公司 | 2019-02-15 | — | — | CN | disclosed |
| CN-104795250-B | printed battery device | 印制能源技术有限公司 | 2019-01-18 | — | — | CN | disclosed |
| CN-108417401-A | Diatomite energy accumulating device | 印制能源技术有限公司 | 2018-08-17 | — | — | CN | disclosed |
| CN-104584160-B | Energy storage device and ink for printing thin film | 印制能源技术有限公司 | 2018-03-23 | — | — | CN | disclosed |
| WO-2004058695-A1 | NOVEL INTERMEDIATES FOR SYNTHESIS OF CEPHALOSPORINS AND PROCESS FOR PREPARATION OF SUCH INTERMEDIATES | LUPIN LIMITED (IN) | 2004-07-15 | — | — | WO | disclosed |
| WO-2004039811-A2 | A METHOD FOR MANUFACTURE OF CEFTIOFUR | LUPIN LIMITED (IN) | 2004-05-13 | — | — | WO | disclosed |
| EP-0791597-B1 | Method for manufacture of cephalosporins and intermediates thereof | LUPIN LAB LTD (IN) | 2000-07-12 | — | — | EP | disclosed |
| US-5945532-A | Method for manufacture of cephalosporin and intermediates thereof | LUPIN LABORATORIES LIMITED (IN) | 1999-08-31 | — | — | US | disclosed |
| US-5856502-A | Method for manufacture of cephalosporin and intermediates thereof | LUPIN LABORATORIES LIMITED (IN) | 1999-01-05 | — | — | US | disclosed |
| US-5739346-A | Dimethyl formiminium chloride chlorosulphate derivatives useful as intermediates for producing cephalosporins | LUPIN LABORATORIES LIMITED (IN) | 1998-04-14 | — | — | US | disclosed |
| US-5739346-A | Dimethyl formiminium chloride chlorosulphate derivatives useful as intermediates for producing cephalosporins | LUPIN LABORATORIES LIMITED (IN) | 1998-04-14 | — | — | US | disclosed |
| EP-0791596-A1 | Method for manufacture of cephalosporins and intermediates thereof | LUPIN LABORATORIES LIMITED (IN) | 1997-08-27 | — | — | EP | disclosed |
| EP-0791597-A1 | Method for manufacture of cephalosporins and intermediates thereof | LUPIN LABORATORIES LIMITED (IN) | 1997-08-27 | — | — | EP | disclosed |
| US-3979454-A | Process for the production of alkyl sulphonic acid hydroxy alkyl amides | BAYER AKTIENGESELLSCHAFT (DT) | 1976-09-07 | — | — | US | disclosed |