Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Dioxane. 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 | |
|---|---|---|---|---|
| Dioxane SCHEMBL27953265 | 0.94 | — | — | |
| SCHEMBL31282317 | 0.94 | TTR (0.86) | — | |
| SCHEMBL31282610 | 0.94 | TTR (0.86) | — | |
| Oxirane SCHEMBL10910379 | 0.94 | — | — | |
| SCHEMBL31282114 | 0.94 | TTR (0.86) | — | |
| Dioxane SCHEMBL10387243 | 0.88 | — | — | |
| Dioxane SCHEMBL21753888 | 0.88 | — | — | |
| Dioxane SCHEMBL1591627 | 0.88 | — | — | |
| Dioxane SCHEMBL5006843 | 0.88 | — | — | |
| SCHEMBL1119 | 0.87 | TTR (1.00) | — |
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 101 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108658834-B | Preparation method of indolone derivative | 烟台药物研究所 | 2021-03-23 | — | — | CN | claimed |
| CN-114835691-B | Benzimidazole derivative and application thereof | 江苏天士力帝益药业有限公司 | 2024-08-20 | — | — | CN | disclosed |
| US-20240239803-A1 | SYNTHESIS OF COELENTERAZINE | INTERNATIONAL PAPER COMPANY | 2024-07-18 | — | — | US | disclosed |
| EP-4344689-A2 | SYNTHESIS OF COELENTERAZINE | International Paper Company (US) | 2024-04-03 | — | — | EP | disclosed |
| US-11939332-B2 | Synthesis of coelenterazine | INTERNATIONAL PAPER COMPANY (US) | 2024-03-26 | — | — | US | disclosed |
| US-11926624-B2 | Synthesis of coelenterazine synthesis intermediate | INTERNATIONAL PAPER COMPANY (US) | 2024-03-12 | — | — | US | disclosed |
| EP-3966214-B1 | SYNTHESIS OF COELENTERAZINE | INT PAPER CO (US) | 2023-12-13 | — | — | EP | disclosed |
| EP-3964509-B1 | COMPOUND CONTAINING FUSED RING, USE THEREOF AND PHARMACEUTICAL COMPOSITION CONTAINING SAME | NANJING HEPO PHARMACEUTICAL CO LTD (CN) | 2023-06-14 | — | — | EP | disclosed |
| US-11661420-B2 | Compound containing fused ring, use thereof and pharmaceutical composition containing same | NANJING HEPO PHARMACEUTICAL CO., LTD (CN) | 2023-05-30 | — | — | US | disclosed |
| CN-114835691-A | Benzimidazole derivative and application thereof | 江苏天士力帝益药业有限公司 | 2022-08-02 | — | — | CN | disclosed |
| EP-0492667-A1 | 1,4-Benzothiazine-2-acetic acid derivatives, processes for production thereof and their use | THE GREEN CROSS CORPORATION (JP) | 1992-07-01 | — | — | EP | disclosed |
| US-4829053-A | Amino acid derivatives | MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) | 1989-05-09 | — | — | US | disclosed |
| EP-0160036-A4 | NOVEL SYNTHETIC METHODS FOR NON-IONIC RADIOGRAPHIC CONTRAST MEDIA. | BIOPHYSICA FOUNDATION (US) | 1987-06-11 | — | — | EP | disclosed |
| EP-0160036-A1 | NOVEL SYNTHETIC METHODS FOR NON-IONIC RADIOGRAPHIC CONTRAST MEDIA | BIOPHYSICA FOUNDATION (US) | 1985-11-06 | — | — | EP | disclosed |
| WO-1985001727-A1 | NOVEL SYNTHETIC METHODS FOR NON-IONIC RADIOGRAPHIC CONTRAST MEDIA | BIOPHYSICA FOUNDATION (US) | 1985-04-25 | — | — | WO | disclosed |
| EP-0073826-A1 | RAPID SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES USING PHOSPHORUS OXYCHLORIDE ACTIVATION | BIORESEARCH INC. (US) | 1983-03-16 | — | — | EP | disclosed |
| WO-1982003079-A1 | RAPID SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES USING PHOSPHORUS OXYCHLORIDE ACTIVATION | BIORESEARCH INC (US) | 1982-09-16 | — | — | WO | disclosed |
| US-4104053-A | 3-Benzyl-2-methylimino-5-phenyl-Δ4 -1,3,4-thiadiazolines and method of combating undesired plant growth | GULF OIL CORPORATION (US) | 1978-08-01 | — | — | US | disclosed |
| US-4020078-A | HERBICIDES | GULF OIL CORPORATION (US) | 1977-04-26 | — | — | US | disclosed |
| US-4010279-A | BIPHENYLOXY DERIVATIVES AND ANTIHYPERLIPIDEMIC USE | BOEHRINGER INGELHEIM GMBH (DT) | 1977-03-01 | — | — | US | disclosed |