⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| SCHEMBL16569192 | 0.60 | — | — | |
| SCHEMBL16179067 | 0.57 | — | — | |
| SCHEMBL2780812 | 0.57 | — | — | |
| SCHEMBL141953 | 0.57 | — | — | |
| SCHEMBL2788228 | 0.55 | — | — | |
| SCHEMBL14606241 | 0.55 | — | — | |
| SCHEMBL10770584 | 0.55 | — | — | |
| SCHEMBL5378417 | 0.55 | — | — | |
| Dioxane SCHEMBL7554059 | 0.46 | — | — | |
| Oxirane SCHEMBL11492072 | 0.41 | — | — |
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 17 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0994882-B1 | MANUFACTURE OF OPTICALLY ACTIVE HALOHYDRIN TRIALKYLSILYL ETHERS | DU PONT (US) | 2003-09-10 | — | — | EP | claimed |
| US-6207847-B1 | REACTING AN EPOXIDE WITH AN AZIDOTRIMETHYLSILANE; THEN HYDROCARBON HALIDE | E. I. DU PONT DE NEMOURS AND COMPANY | 2001-03-27 | — | — | US | claimed |
| EP-0994882-A1 | MANUFACTURE OF OPTICALLY ACTIVE HALOHYDRIN TRIALKYLSILYL ETHERS | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2000-04-26 | — | — | EP | claimed |
| WO-1999002535-A1 | MANUFACTURE OF OPTICALLY ACTIVE HALOHYDRIN TRIALKYLSILYL ETHERS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-01-21 | — | — | WO | claimed |
| EP-0994882-B1 | MANUFACTURE OF OPTICALLY ACTIVE HALOHYDRIN TRIALKYLSILYL ETHERS | DU PONT (US) | 2003-09-10 | — | — | EP | disclosed |
| US-6207847-B1 | REACTING AN EPOXIDE WITH AN AZIDOTRIMETHYLSILANE; THEN HYDROCARBON HALIDE | E. I. DU PONT DE NEMOURS AND COMPANY | 2001-03-27 | — | — | US | disclosed |
| EP-0994882-A1 | MANUFACTURE OF OPTICALLY ACTIVE HALOHYDRIN TRIALKYLSILYL ETHERS | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2000-04-26 | — | — | EP | disclosed |
| US-5990135-A | FOR TREATING A RETROVIRAL INFECTION SUCH AS HIV INFECTION; FOR EXAMPLE 5S-N-((2-PYRIDINYL)METHOXYCARBONYL)VALINYLAMINO-2-((N-3 -PYRIDINYL)METHOXYCARBONYL)AMINO-4S-HYDROXY-1,6-DIPHENYL-2-AZAHEXANE AND OTHER COMPOUNDS OF GIVEN FORMULA | ABBOTT LABORATORIES (US) | 1999-11-23 | — | — | US | disclosed |
| WO-1999002535-A1 | MANUFACTURE OF OPTICALLY ACTIVE HALOHYDRIN TRIALKYLSILYL ETHERS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1999-01-21 | — | — | WO | disclosed |
| US-5631376-A | PEPTIDE DERIVATIVES FOR TREATMENT OF AIDS | ABBOTT LABORATORIES (US) | 1997-05-20 | — | — | US | disclosed |
| US-5621109-A | OXAZOLE/THIAZOLE DERIVATIVES OF HYDROXYMETHYL HYDRAZONES; SIDE EFFECT REDUCTION | ABBOTT LABORATORIES (US) | 1997-04-15 | — | — | US | disclosed |
| EP-0683772-A1 | RETROVIRAL PROTEASE INHIBITING COMPOUNDS | ABBOTT LABORATORIES (US) | 1995-11-29 | — | — | EP | disclosed |
| US-5461067-A | For HIV infections | ABBOTT LABORATORIES (US) | 1995-10-24 | — | — | US | disclosed |
| EP-0683772-A4 | RETROVIRAL PROTEASE INHIBITING COMPOUNDS. | ABBOTT LAB (US) | 1995-09-27 | — | — | EP | disclosed |
| WO-1994019332-A1 | RETROVIRAL PROTEASE INHIBITING COMPOUNDS | ABBOTT LABORATORIES (US) | 1994-09-01 | — | — | WO | disclosed |
| US-5086189-A | PROCESS FOR THE MANUFACTURE OF EPOXIDES | INTEROX (SOCIETE ANONYME) (BE) | 1992-02-04 | — | — | US | disclosed |
| EP-0068564-A1 | Process for the preparation of epoxides | INTEROX Société Anonyme (BE) | 1983-01-05 | — | — | EP | disclosed |