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 SCHEMBL28151108 | 1.00 | ALDH1A1 (0.91) | — | |
| Hydrochloric Acid SCHEMBL6746921 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL28899252 | 0.96 | — | — | |
| SCHEMBL1330344 | 0.95 | — | — | |
| SCHEMBL523 | 0.95 | — | — | |
| SCHEMBL5305593 | 0.95 | ALDH1A1 (1.00) | — | |
| SCHEMBL1331977 | 0.95 | — | — | |
| SCHEMBL1331774 | 0.95 | — | — | |
| SCHEMBL9866292 | 0.95 | — | — | |
| SCHEMBL10341165 | 0.91 | — | — |
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 59 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-111960986-A | Preparation method of acemetacin | 河南东泰制药有限公司 | 2020-11-20 | — | — | CN | claimed |
| US-6891050-B2 | Process for the preparation of taxanes such as paclitaxel, docetaxel and structurally similar analogs | DABUR INDIA LIMITED (IN) | 2005-05-10 | — | — | US | claimed |
| CN-1480440-A | Technique for producing chloroactic acid through hthp method and its equipment | 何 正 | 2004-03-10 | — | — | CN | claimed |
| US-20030045732-A1 | Process for the preparation of taxanes such as paclitaxel, docetaxel and structurally similar analogs | DABUR PHARMA LIMITED (IN) | 2003-03-06 | — | — | US | claimed |
| CN-120037794-A | Preparation method and application of solvent-resistant polyamide composite membrane | 南京工业大学 | 2025-05-27 | — | — | CN | disclosed |
| CN-118401587-A | Curable resin composition, resin sheet, and cured product thereof | 日本化药株式会社 | 2024-07-26 | — | — | CN | disclosed |
| US-20230167051-A1 | A PROCESS FOR SYNTHESIS OF HIGH PURITY l-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE OXIME | LAXMI ORGANIC INDUSTRIES LTD (IN) | 2023-06-01 | — | — | US | disclosed |
| EP-4110750-A1 | A PROCESS FOR SYNTHESIS OF HIGH PURITY 1-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE OXIME | Laxmi Organic Industries Limited (IN) | 2023-01-04 | — | — | EP | disclosed |
| CN-111960986-A | Preparation method of acemetacin | 河南东泰制药有限公司 | 2020-11-20 | — | — | CN | disclosed |
| CN-111960986-A | Preparation method of acemetacin | 河南东泰制药有限公司 | 2020-11-20 | — | — | CN | disclosed |
| CN-111704630-A | 3-arylformyl naphtho-isoxazole or 3-arylformyl anthraceno-isoxazole derivative and synthetic method thereof | 上海大学 | 2020-09-25 | — | — | CN | disclosed |
| CN-108707098-A | Compound and its preparation method and application containing quaternary ammonium salt ion and peroxycarboxylic acid groups in structure | 史清元 | 2018-10-26 | — | — | CN | disclosed |
| US-4111946-A | Preparation of 3-(pyridinyl)-2-cyclohexen-1-ones | STERLING DRUG INC. (US) | 1978-09-05 | — | — | US | disclosed |
| US-4075012-A | COPOLYMERS OF ACRYLIC ESTER DERIVATIVES | XEROX CORPORATION (US) | 1978-02-21 | — | — | US | disclosed |
| US-4075217-A | Conversion of 3-(pyridinyl)-2-cyclohexen-1-one to 3-(pyridinyl)anilines | STERLING DRUG INC. (US) | 1978-02-21 | — | — | US | disclosed |
| US-4043812-A | ADDITION POLYMERS, FILMS, PHOTOCONDUCTIVITY | XEROX CORPORATION (US) | 1977-08-23 | — | — | US | disclosed |
| US-4026900-A | 3-(Pyridinyl)-2-cyclohexen-1-ones | STERLING DRUG INC. (US) | 1977-05-31 | — | — | US | disclosed |
| US-4025710-A | Intrachain charge transfer complexes | XEROX CORPORATION (US) | 1977-05-24 | — | — | US | disclosed |
| US-4013623-A | FREE RADICAL COPOLYMERIZATION, ELECTROGRAPHY | XEROX CORPORATION (US) | 1977-03-22 | — | — | US | disclosed |
| US-4007043-A | Photoconductive elements with copolymer charge transport layers | XEROX CORPORATION (US) | 1977-02-08 | — | — | US | disclosed |