⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL6207080 | 1.00 | — | — | |
| SCHEMBL818468 | 0.83 | — | — | |
| SCHEMBL818467 | 0.83 | — | — | |
| SCHEMBL819793 | 0.83 | — | — | |
| SCHEMBL16369047 | 0.73 | TSHR (0.53) | — | |
| SCHEMBL9882909 | 0.73 | — | — | |
| SCHEMBL8273303 | 0.73 | — | — | |
| SCHEMBL7230172 | 0.71 | — | — | |
| SCHEMBL5311436 | 0.71 | — | — | |
| SCHEMBL13660116 | 0.71 | — | — |
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 |
|---|---|---|---|---|---|---|---|
| CN-111668549-B | Additive for electrolyte, electrolyte and battery material | 广州天赐高新材料股份有限公司 | 2021-07-06 | — | — | CN | disclosed |
| CN-111668549-A | Additive for electrolyte, electrolyte and battery material | 广州天赐高新材料股份有限公司 | 2020-09-15 | — | — | CN | disclosed |
| EP-0948512-B1 | METHOD OF SYNTHESIZING PHOSPHOROTHIOATE OLIGONUCLEOTIDES | ISIS PHARMACEUTICALS INC (US) | 2004-10-06 | — | — | EP | disclosed |
| US-6780989-B2 | HYBRID OLIGONUCLEOTIDE | ISIS PHARMACEUTICALS, INC. | 2004-08-24 | — | — | US | disclosed |
| EP-0983233-B1 | REAGENT USEFUL FOR SYNTHESIZING SULFURIZED OLIGONUCLEOTIDE ANALOGS | ISIS PHARMACEUTICALS INC (US) | 2004-05-06 | — | — | EP | disclosed |
| US-20030114662-A1 | Method of synthesizing phosphorothioate oligonucleotides | ISIS PHARMACEUTICALS, INC. | 2003-06-19 | — | — | US | disclosed |
| US-20020128466-A1 | Method of synthesizing phosphorothioate oligonucleotides | ISIS PHARMACEUTICALS, INC. | 2002-09-12 | — | — | US | disclosed |
| US-6403781-B2 | REACTING A PHOSPHORDIAMIDITE WITH A SUPPORT-BOUND SYNTHON TO FORM A SUPPORT BOUND PHOSPHORAMIDITE, PROTECTING TO FORM A SUPPORT BOUND PHOSHITE, SULFURIZING THE PHOSPHITE TO FORM A PROTECTED PHOSPHORTHIOATE AND DEPROTECTING | ISIS PHARMACEUTICALS, INC. | 2002-06-11 | — | — | US | disclosed |
| US-6399831-B1 | THIODICARBONIC ACID DIESTER POLYSULFIDE | ISIS PHARMACEUTICALS, INC. | 2002-06-04 | — | — | US | disclosed |
| US-20010003132-A1 | Method of synthesizing phosphorothioate oligonucleotides | ISIS PHARMACEUTICALS, INC. | 2001-06-07 | — | — | US | disclosed |
| US-5760209-A | Protecting group for synthesizing oligonucleotide analogs | ISIS PHARMACEUTICALS, INC. (US) | 1998-06-02 | — | — | US | disclosed |
| US-5708180-A | CYCLIZATION OF UNSATURATED NITRILE, AMIDE OR OXIME | BAYER AKTIENGESELLSCHAFT (DE) | 1998-01-13 | — | — | US | disclosed |
| US-5705621-A | Oligomeric phosphite, phosphodiester, Phosphorothioate and phosphorodithioate compounds and intermediates for preparing same | ISIS PHARMACEUTICALS, INC. (US) | 1998-01-06 | — | — | US | disclosed |
| US-5637751-A | REACTING IN LIQUID PHASE 2-BUTENE-1,4-DIOL AND/OR 3-BUTENE-1,2-DIOL WITH HYDROGEN CYANIDE IN PRESENCE OF MOLTEN CATALYST COMPRISING CUPROUS CHLORIDE OR BROMIDE AND NON-AROMATIC AMINE HYDROHALIDE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1997-06-10 | — | — | US | disclosed |
| EP-0612720-B1 | Process for producing 1,4-dicyano-2-butene | SUMITOMO CHEMICAL CO (JP) | 1997-01-08 | — | — | EP | disclosed |
| EP-0563859-B1 | Process for producing 1,4-dicyano-2-butene and catalyst therefor | SUMITOMO CHEMICAL CO (JP) | 1996-09-11 | — | — | EP | disclosed |
| EP-0702003-A2 | Process for preparing 2-halogenpyridinaldehydes and new 2-halogenpyridinaldehydes | BAYER AG (DE) | 1996-03-20 | — | — | EP | disclosed |
| US-5463103-A | Reacting butene derivative with hydrogen cyanide in presence of catalyst prepared from cuprous halide, lower alkylamine hydrohalide and Lewis acid or basic acetate, carbonate or bicarbonate | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1995-10-31 | — | — | US | disclosed |
| EP-0612720-A1 | Process for producing 1,4-dicyano-2-butene | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1994-08-31 | — | — | EP | disclosed |
| EP-0563859-A2 | Process for producing 1,4-dicyano-2-butene and catalyst therefor | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-10-06 | — | — | EP | disclosed |