SCHEMBL848249

SCHEMBL848249

CCCCC=CC#N

nearest known ligand 0.00

⚠ 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.

Compoundsimilaritytop predictedshared targets
SCHEMBL848248 1.00
SCHEMBL2253325 1.00
SCHEMBL18941502 0.95 FAAH (0.38)
SCHEMBL18941607 0.95 TRPV1 (0.39)
SCHEMBL18941608 0.95 TRPV1 (0.39)
SCHEMBL18941504 0.95 FAAH (0.38)
SCHEMBL18941484 0.95 FAAH (0.43)
SCHEMBL18941543 0.93 FAAH (0.46)
SCHEMBL18941613 0.93 FAAH (0.46)
SCHEMBL18941545 0.93 FAAH (0.46)

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 70 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110207835-A1 Alpha, Beta, Unsaturated Nitriles as Fragrances GIVAUDAN SA (CH) 2011-08-25 US claimed
EP-2079436-B1 ALPHA, BETA, UNSATURATED NITRILES AS FRAGRANCES GIVAUDAN SA (CH) 2010-11-10 EP claimed
EP-2079436-A1 ALPHA, BETA, UNSATURATED NITRILES AS FRAGRANCES Givaudan SA (CH) 2009-07-22 EP claimed
WO-2008037105-A1 ALPHA, BETA, UNSATURATED NITRILES AS FRAGRANCES GIVAUDAN SA (CH) 2008-04-03 WO claimed
US-20260018621-A1 SECONDARY BATTERY AND ELECTRONIC APPARATUS NINGDE AMPEREX TECHNOLOGY LIMITED (CN) 2026-01-15 US disclosed
CN-109557764-B Chemically amplified positive photosensitive resin composition, resist pattern, method for forming the same, and electronic device 奇美实业股份有限公司 2023-09-12 CN disclosed
EP-3643312-A1 3-[4-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-1H-PYRAZOL-1-YL]OCTANE- OR HEPTANE-NITRILE AS JAK INHIBITORS Incyte Holdings Corporation (US) 2020-04-29 EP disclosed
EP-2432472-B1 3-[4-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-1H-PYRAZOL-1-YL]OCTANE- OR HEPTANE-NITRILE AS JAK INHIBITORS INCYTE HOLDINGS CORP (US) 2019-10-02 EP disclosed
US-9623029-B2 3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]octane- or heptane-nitrile as JAK inhibitors INCYTE HOLDINGS CORPORATION (US) 2017-04-18 US disclosed
US-20160067253-A1 3-[4-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-1H-PYRAZOL-1-YL]OCTANE- OR HEPTANE-NITRILE AS JAK INHIBITORS INCYTE HOLDINGS CORPORATION (US) 2016-03-10 US disclosed
US-9216984-B2 3-[4-(7H-pyrrolo[2,3-D]pyrimidin-4-yl)-1H-pyrazol-1-yl]octane—or heptane-nitrile as JAK inhibitors INCYTE CORPORATION (US) 2015-12-22 US disclosed
US-9023882-B2 5-membered nitrogen containing heterocyclic derivatives and pharmaceutical compositions comprising the same KISSEI PHARMACEUTICAL CO., LTD. (JP) 2015-05-05 US disclosed
EP-0663394-A1 Process for preparing 5-aminodihydropyrrole, intermediate thereof and process for preparing said intermediate SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1995-07-19 EP disclosed
US-5288315-A Aqueous electrodepositable or alkaline paints including a bind binder and a corrosion inhibitor comprising a mono-, di- or polyazo-methine; metal substrates CIBA-GEIGY CORPORATION (US) 1994-02-22 US disclosed
US-4451479-A ANTIINFLAMMATORY AMERICAN CYANAMID COMPANY (US) 1984-05-29 US disclosed
US-4416824-A Recovery of triarylboranes by forming boron-containing metal compounds E. I. DU PONT DE NEMOURS & CO. (US) 1983-11-22 US disclosed
US-4394321-A CHEMICAL INTERMEDIATES E. I. DU PONT DE NEMOURS AND COMPANY (US) 1983-07-19 US disclosed
EP-0070376-A1 Heterocyclic substituted-amino-pyrazolines AMERICAN CYANAMID COMPANY (US) 1983-01-26 EP disclosed
US-4254059-A TO PRIMARY AMINES UNDER MILD CONDITIONS USING A GROUP 8 METAL ANIONIC CATALYST COMPOSITION ALLIED CHEMICAL CORPORATION (US) 1981-03-03 US disclosed
US-4038210-A BETA-AMINO NITRILE CATALYSTS FOR POLYURETHANE PREPARATION UNION CARBIDE CORPORATION (US) 1977-07-26 US disclosed