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 SCHEMBL28130960 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL4806073 | 1.00 | — | — | |
| SCHEMBL6704332 | 0.93 | TP53 (0.31) | — | |
| SCHEMBL98 | 0.93 | — | — | |
| SCHEMBL6068389 | 0.86 | — | — | |
| SCHEMBL10946713 | 0.86 | — | — | |
| SCHEMBL31398318 | 0.86 | — | — | |
| Ammonia Solution, Strong SCHEMBL17188187 | 0.86 | — | — | |
| Water SCHEMBL1292893 | 0.86 | — | — | |
| Lithium SCHEMBL11132311 | 0.86 | — | — |
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 160 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-106565773-B | A kind of preparation method of high-purity phosphoric acid ester fire retardant tricresyl phosphate (2- chloropropyl) ester | 泰州瑞世特新材料有限公司 | 2019-06-14 | — | — | CN | claimed |
| CN-105924625-B | A kind of water white transparency Halogenless fire retarded epoxy resin of low-temperature curable and preparation method thereof | 长春工业大学 | 2018-08-24 | — | — | CN | claimed |
| CN-105924626-B | A kind of halogen-free flameproof curing agent of liquid water white transparency epoxy resin and preparation method thereof | 长春工业大学 | 2018-06-19 | — | — | CN | claimed |
| CN-107722054-A | A kind of vitamin D3Phosphamide and preparation method thereof | 无锡福祈制药有限公司 | 2018-02-23 | — | — | CN | claimed |
| CN-107629248-A | A kind of agent of hyperbranched expandable flame retardant containing phosphine oxide and its preparation method and application | 中国科学技术大学 | 2018-01-26 | — | — | CN | claimed |
| CN-105482430-B | A kind of method that utilization sol-gal process prepares polyethylene glycol phase-change material | 西南科技大学 | 2017-10-03 | — | — | CN | claimed |
| CN-105131037-B | Preparation method for high-purity tedizolid phosphate | 济南爱思医药科技有限公司 | 2017-05-03 | — | — | CN | claimed |
| CN-106279716-A | A kind of P Modification hydroxymethylated lignin carbon forming agent and preparation method thereof | 常州大学 | 2017-01-04 | — | — | CN | claimed |
| CN-102077060-B | Monitoring system based on corrosion metal | G. PATEL (US) | 2014-10-29 | — | — | CN | claimed |
| CN-1055535-A | Synthesizing of 2-hydroxy-n-methyl-N-phenyl-6-naphthalene sulfonylamide | KE BAOGUI (CN) | 1991-10-23 | — | — | CN | claimed |
| EP-4724070-A2 | WRN INHIBITORS | Nimbus Wadjet, Inc. (US) | 2026-04-15 | — | — | EP | disclosed |
| WO-2024254511-A2 | WRN INHIBITORS | NIMBUS WADJET, INC. (US) | 2024-12-12 | — | — | WO | disclosed |
| CN-107188898-B | Process for preparing thienopyrimidine compounds | 霍夫曼-拉罗奇有限公司 | 2019-12-03 | — | — | CN | disclosed |
| CN-105980384-B | Macrocyclic compounds having a heterocyclic P2' group as factor XIA inhibitors | 百时美施贵宝公司 | 2019-11-15 | — | — | CN | disclosed |
| CN-105705492-B | 5,6,7, 8-tetrahydro-5, 8-methanocinnoline derivatives as RORC modulators for the treatment of autoimmune diseases | 豪夫迈·罗氏有限公司 | 2019-11-05 | — | — | CN | disclosed |
| CN-1220029-A | Incombustible/self-extinguishing battery electrolyte | STANFORD RES INST INT (US) | 1999-06-16 | — | — | CN | disclosed |
| CN-1179713-A | Use of LCK SH2 specific compounds to treat autoimmune diseases and allograft rejection | SMITHKLINE BEECHAM CORP (US) | 1998-04-22 | — | — | CN | disclosed |
| WO-1997048279-A1 | AGENTS WITH ANTIFUNGAL ACTIVITY AND METHODS OF USE THEREOF | UNIVERSITY OF ALBERTA (US) | 1997-12-24 | — | — | WO | disclosed |
| CN-1055535-A | Synthesizing of 2-hydroxy-n-methyl-N-phenyl-6-naphthalene sulfonylamide | KE BAOGUI (CN) | 1991-10-23 | — | — | CN | disclosed |
| CN-1055535-A | Synthesizing of 2-hydroxy-n-methyl-N-phenyl-6-naphthalene sulfonylamide | KE BAOGUI (CN) | 1991-10-23 | — | — | CN | disclosed |