SCHEMBL16532750

SCHEMBL16532750

Cc1cc(N2CC(CC#N)(n3cc(-c4ncnc5[nH]ccc45)cn3)C2)c(F)cc1C(=O)N[C@@H](C)C(F)(F)F

nearest known ligand 0.80

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ JAK2 O60674 18/20 0.80
▸ JAK1 P23458 3/20 0.62
▸ AXL P30530 2/20 0.62
▸ PIK3CD O00329 1/20 0.62
▸ TYRO3 Q06418 1/20 0.62
▸ MERTK Q12866 1/20 0.62

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL29379586 0.95 JAK2 (0.84) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL21412834 0.95 JAK2 (0.84) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL14377767 0.95 JAK2 (0.84) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL14376756 0.95 JAK2 (0.84) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL22449882 0.93 JAK2 (0.80) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL22449884 0.93 JAK2 (0.79) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL22622522 0.93 JAK2 (0.79) JAK2JAK1AXLPIK3CDTYRO3
SCHEMBL14377572 0.91 JAK2 (0.82) JAK2JAK1AXL
SCHEMBL21799144 0.91 JAK2 (0.82) JAK2JAK1AXL
SCHEMBL14377481 0.91 JAK2 (0.82) JAK2JAK1AXL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024030600-A1 TREATMENT OF URTICARIA USING JAK INHIBITORS INCYTE CORPORATION (US) 2024-02-08 — — WO disclosed
WO-2022150676-A1 COMBINATION THERAPY COMPRISING JAK PATHWAY INHIBITOR AND ROCK INHIBITOR INCYTE CORPORATION (US) 2022-07-14 — — WO disclosed
WO-2022125670-A1 JAK1 PATHWAY INHIBITORS FOR THE TREATMENT OF VITILIGO INCYTE CORPORATION (US) 2022-06-16 — — WO disclosed
EP-3371190-B1 HETEROCYCLIC COMPOUNDS AS PI3K-GAMMA INHIBITORS INCYTE CORP (US) 2022-03-30 — — EP disclosed
WO-2021076124-A1 USE OF JAK1 INHIBITORS FOR THE TREATMENT OF CUTANEOUS LUPUS ERYTHEMATOSUS AND LICHEN PLANUS (LP) INCYTE CORPORATION (US) 2021-04-22 — — WO disclosed
WO-2021072098-A1 BIOMARKERS FOR GRAFT-VERSUS-HOST DISEASE INCYTE CORPORATION (US) 2021-04-15 — — WO disclosed
WO-2021072116-A1 BIOMARKERS FOR GRAFT-VERSUS-HOST DISEASE INCYTE CORPORATION (US) 2021-04-15 — — WO disclosed
WO-2020191041-A2 BIOMARKERS FOR VITILIGO INCYTE CORPORATION (US) 2020-09-24 — — WO disclosed
WO-2020132210-A1 JAK1 PATHWAY INHIBITORS FOR THE TREATMENT OF GASTROINTESTINAL DISEASE INCYTE CORPORATION (US) 2020-06-25 — — WO disclosed
WO-2019200030-A1 BIOMARKERS FOR GRAFT-VERSUS-HOST DISEASE INCYTE CORPORATION (US) 2019-10-17 — — WO disclosed
WO-2017027717-A1 BICYCLIC FUSED PYRIMIDINE COMPOUNDS AS TAM INHIBITORS INCYTE CORPORATION (US) 2017-02-16 — — WO disclosed
WO-2016183060-A1 PROCESS FOR THE SYNTHESIS OF A PHOSPHOINOSITIDE 3-KINASE INHIBITOR INCYTE CORPORATION (US) 2016-11-17 — — WO disclosed
WO-2016183062-A1 SALTS OF (S)-7-(1-(9H-PURIN-6-YLAMINO)ETHYL)-6-(3-FLUOROPHENYL)-3-METHYL-5H-THIAZOLO[3,2-A]PYRIMIDIN-5-ONE INCYTE CORPORATION (US) 2016-11-17 — — WO disclosed
WO-2016183063-A1 CRYSTALLINE FORMS OF A PI3K INHIBITOR INCYTE CORPORATION (US) 2016-11-17 — — WO disclosed
WO-2016138363-A1 SALTS OF PI3K INHIBITOR AND PROCESSES FOR THEIR PREPARATION INCYTE CORPORATION (US) 2016-09-01 — — WO disclosed
WO-2015191677-A1 BICYCLIC HETEROARYLAMINOALKYL PHENYL DERIVATIVES AS PI3K INHIBITORS INCYTE CORPORATION (US) 2015-12-17 — — WO disclosed
WO-2015184305-A1 TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 INCYTE CORPORATION (US) 2015-12-03 — — WO disclosed
WO-2015157257-A1 TREATMENT OF B-CELL MALIGNANCIES BY A COMBINATION JAK AND PI3K INHIBITOR INCYTE CORPORATION (US) 2015-10-15 — — WO disclosed
WO-2015131031-A1 JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES INCYTE CORPORATION (US) 2015-09-03 — — WO disclosed
WO-2015026818-A1 SURVIVAL BENEFIT IN PATIENTS WITH SOLID TUMORS WITH ELEVATED C-REACTIVE PROTEIN LEVELS INCYTE CORPORATION (US) 2015-02-26 — — WO disclosed
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