SCHEMBL2395720

SCHEMBL2395720

N#CCC1(n2cc(-c3ncnc4[nH]ccc34)cn2)CN(C2CCN(C(=O)Nc3ccc(F)cc3C(F)(F)F)CC2)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
JAK2 O60674 20/20 1.00
AXL P30530 1/20 1.00
JAK1 P23458 7/20 0.83

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
SCHEMBL29374300 1.00 JAK2 (1.00) JAK2AXLJAK1
SCHEMBL29422183 0.93 JAK2 (1.00) JAK2AXLJAK1
SCHEMBL2394032 0.93 JAK2 (1.00) JAK2AXLJAK1
SCHEMBL12310931 0.92 JAK2 (0.85) JAK2AXLJAK1
SCHEMBL22826757 0.92 JAK2 (0.84) JAK2AXLJAK1
SCHEMBL29422246 0.92 JAK2 (1.00) JAK2AXLJAK1
SCHEMBL2396578 0.92 JAK2 (1.00) JAK2AXLJAK1
SCHEMBL21412809 0.91 JAK2 (0.84) JAK2AXLJAK1
SCHEMBL2394503 0.91 JAK2 (1.00) JAK2AXLJAK1
SCHEMBL2392065 0.91 JAK2 (1.00) JAK2AXLJAK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4400172-A2 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS Incyte Holdings Corporation (US) 2024-07-17 EP claimed
EP-3773593-B1 TREATMENT OF HIDRADENITIS SUPPURATIVA USING JAK INHIBITORS INCYTE CORP (US) 2024-05-15 EP claimed
EP-4036088-B1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS INCYTE HOLDINGS CORP (US) 2024-04-03 EP claimed
US-20240091234-A1 TREATMENT OF B-CELL MALIGNANCIES BY A COMBINATION JAK AND PI3K INHIBITORS INCYTE CORPORATION 2024-03-21 US claimed
CN-117120055-A Combination therapy comprising a JAK pathway inhibitor and a ROCK inhibitor 因赛特公司 2023-11-24 CN claimed
US-20230043959-A1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS INCYTE CORPORATION 2023-02-09 US claimed
US-20220378791-A1 JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES INCYTE CORPORATION 2022-12-01 US claimed
US-20220241286-A1 TREATMENT OF HIDRADENITIS SUPPURATIVA USING JAK INHIBITORS INCYTE CORPORATION 2022-08-04 US claimed
US-20220226327-A1 COMBINATION THERAPY COMPRISING JAK PATHWAY INHIBITOR AND ROCK INHIBITOR INCYTE CORPORATION 2022-07-21 US claimed
US-11324749-B2 Combination therapy for treatment of hematological diseases INCYTE CORPORATION (US) 2022-05-10 US claimed
EP-2545045-B1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS INCYTE HOLDINGS CORP (US) 2016-01-06 EP claimed
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 claimed
US-20150342952-A1 TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 INCYTE CORPORATION (US) 2015-12-03 US claimed
WO-2015131031-A1 JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES INCYTE CORPORATION (US) 2015-09-03 WO claimed
US-20150246046-A1 JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES INCYTE CORPORATION 2015-09-03 US claimed
US-20150065447-A1 SURVIVAL BENEFIT IN PATIENTS WITH SOLID TUMORS WITH ELEVATED C-REACTIVE PROTEIN LEVELS INCYTE CORPORATION (US) 2015-03-05 US claimed
CN-102985417-A Piperidin-4-yl azetidine derivatives as JAK1 inhibitors INCYTE CORP 2013-03-20 CN claimed
EP-2545045-A1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS Incyte Corporation (US) 2013-01-16 EP claimed
US-20110224190-A1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS INCYTE CORPORATION 2011-09-15 US claimed
WO-2011112662-A1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS INCYTE CORPORATION (US) 2011-09-15 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (10 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20220378791-A1 JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES JAK1, JAK2, JAK3 JAK2 2/4885AXL 1052/4885JAK1 1/4885
US-20150065447-A1 SURVIVAL BENEFIT IN PATIENTS WITH SOLID TUMORS WITH ELEVATED C-REACTIVE PROTEIN LEVELS JAK2, STAT3, IL6 JAK2 1/4885AXL 589/4885JAK1 4/4885
US-20150246046-A1 JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES JAK1, JAK2, JAK3 JAK2 2/4885AXL 1052/4885JAK1 1/4885
US-20150342952-A1 TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 JAK1, JAK2, MCL1 JAK2 2/4885AXL 1833/4885JAK1 1/4885
US-20220241286-A1 TREATMENT OF HIDRADENITIS SUPPURATIVA USING JAK INHIBITORS JAK1, JAK2, JAK3 JAK2 2/4885AXL 2137/4885JAK1 1/4885
US-20240091234-A1 TREATMENT OF B-CELL MALIGNANCIES BY A COMBINATION JAK AND PI3K INHIBITORS JAK2, JAK1, BTK JAK2 1/4885AXL 889/4885JAK1 2/4885
US-20220226327-A1 COMBINATION THERAPY COMPRISING JAK PATHWAY INHIBITOR AND ROCK INHIBITOR JAK1, ROCK1, JAK3 JAK2 8/4885AXL 1369/4885JAK1 1/4885
US-11324749-B2 Combination therapy for treatment of hematological diseases JAK1, JAK3, JAK2 JAK2 3/4885AXL 1288/4885JAK1 1/4885
US-20110224190-A1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS JAK1, JAK2, JAK3 JAK2 2/4885AXL 2549/4885JAK1 1/4885
US-20230043959-A1 PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS JAK1, JAK2, JAK3 JAK2 2/4885AXL 2691/4885JAK1 1/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.