SCHEMBL2010687

SCHEMBL2010687

O=CN1CC(F)(F)C1

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
SCHEMBL490276 0.78
SCHEMBL31659650 0.78
SCHEMBL22602659 0.77
SCHEMBL3342266 0.76
SCHEMBL23874212 0.75
SCHEMBL13175590 0.71
SCHEMBL286213 0.71 HSD17B10 (0.30)
SCHEMBL22319209 0.70
SCHEMBL22595178 0.69
SCHEMBL21929852 0.69

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12006320-B2 Heterocyclic derivatives as PI3K inhibitors INCYTE CORPORATION (US) 2024-06-11 US claimed
CN-117529320-A ROCK2 inhibitors for the treatment of viral infections 格雷威顿生物科技有限公司 2024-02-06 CN claimed
WO-2023165591-A1 COMPOUNDS AND THEIR USES AS LPAR5 ANTAGONISTS IMMUTHER PHARMATECH (SHANGHAI) CO., LTD. (CN) 2023-09-07 WO claimed
CN-111278817-B Polycyclic compounds as farnesol X receptor modulators 百时美施贵宝公司 2023-05-16 CN claimed
WO-2022216655-A1 N-(6-((OCTAHYDROCYCLOPENTA[C]PYRROL-5-YI)AMINO)PYRIDAZIN-3-YL)PHENYL)CARBOXAMIDE AND (6- ((OCTAHYDROCYCLOPENTA[C]PYRROL-5-YL)AMINO)PYRIDAZIN-3-YL)BENZAMIDE DERIVATIVES AS MACHR M4 ANTAGONISTS FOR THE TREATMENT OF NEURODEGENERATIVE DISORDERS VANDERBILT UNIVERSITY (US) 2022-10-13 WO claimed
US-11396502-B2 Substituted heterocyclic derivatives as PI3K inhibitors INCYTE CORPORATION (US) 2022-07-26 US claimed
US-20210395258-A1 HETEROCYCLIC DERIVATIVES AS PI3K INHIBITORS INCYTE CORPORATION 2021-12-23 US claimed
CN-113412113-A Aminooxazine amides 豪夫迈·罗氏有限公司 2021-09-17 CN claimed
US-11078204-B2 Heterocyclic derivatives as PI3K inhibitors INCYTE CORPORATION (US) 2021-08-03 US claimed
WO-2020102198-A1 HETEROCYCLIC DERIVATIVES AS PI3K INHIBITORS INCYTE CORPORATION (US) 2020-05-22 WO claimed
WO-2020102216-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES AS PI3K INHIBITORS INCYTE CORPORATION (US) 2020-05-22 WO claimed
US-20200148689-A1 HETEROCYCLIC DERIVATIVES AS PI3K INHIBITORS INCYTE CORPORATION 2020-05-14 US claimed
US-20200148667-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES AS PI3K INHIBITORS INCYTE CORPORATION 2020-05-14 US claimed
EP-3004086-A1 SUBSTITUTED BENZOXAZOLES Bayer Pharma Aktiengesellschaft (DE) 2016-04-13 EP claimed
WO-2014205393-A1 NUCLEAR TRANSPORT MODULATORS AND USES THEREOF Karyopharm Therapeutics Inc. (US) 2014-12-24 WO claimed
WO-2014195230-A1 SUBSTITUTED BENZOXAZOLES BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2014-12-11 WO claimed
CN-103517903-A Pyrrolopyridineamino derivatives as MPS1 inhibitors CANCER REC TECH LTD 2014-01-15 CN claimed
WO-2011073273-A1 BENZOXAZINE ARYL SULFONAMIDE DERIVATIVES AS KV1.3 MODULATORS EVOTEC AG (DE) 2011-06-23 WO claimed
CN-122094667-A Formulations and uses of ROCK2 inhibitors for ALS 2026-05-26 CN disclosed
CN-102083804-A 5-phenyl-isoxazole-3-carboxamides modulating HSP90 with antitumoral activities SIGMA TAU RES SWITZERLAND SA 2011-06-01 CN disclosed