SCHEMBL265061

SCHEMBL265061

Cc1cnc(Nc2ccc(N3CCN(C)CC3)cc2)nc1Nc1cccc(S(=O)(=O)NC(C)(C)C)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
BRD4 O60885 20/20 1.00
JAK2 O60674 3/20 1.00
FLT3 P36888 2/20 1.00
JAK1 P23458 2/20 1.00
BRD2 P25440 2/20 1.00
JAK3 P52333 2/20 1.00
BRD3 Q15059 2/20 1.00
BRDT Q58F21 2/20 1.00
BUB1B O60566 1/20 1.00
RET P07949 1/20 1.00
WEE1 P30291 1/20 1.00
ALK Q9UM73 1/20 1.00

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
SCHEMBL31163083 1.00 BRD4 (1.00) BRD4JAK2FLT3JAK1BRD2
SCHEMBL29432552 1.00 BRD4 (1.00) BRD4JAK2FLT3JAK1BRD2
SCHEMBL14536137 0.94 BRD4 (0.89) BRD4JAK2FLT3JAK1BRD2
SCHEMBL31163086 0.92 BRD4 (0.85) BRD4JAK2FLT3JAK1BRD2
SCHEMBL271198 0.92 BRD4 (0.85) BRD4JAK2FLT3JAK1BRD2
SCHEMBL30306487 0.91 BRD4 (1.00) BRD4JAK2FLT3JAK1BRD2
SCHEMBL17526335 0.91 BRD4 (1.00) BRD4JAK2FLT3JAK1BRD2
SCHEMBL263665 0.91 BRD4 (0.84) BRD4JAK2FLT3JAK1BRD2
SCHEMBL17526085 0.91 BRD4 (1.00) BRD4JAK2FLT3JAK1BRD2
SCHEMBL270925 0.91 BRD4 (0.83) BRD4JAK2FLT3JAK1BRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260097028-A1 Methods of Treating Myeloproliferative Neoplasms KARTOS THERAPEUTICS INC (US) 2026-04-09 US claimed
EP-4673149-A1 NEW COMPOUNDS AND TREATMENT OF RENAL CELL CARCINOMA Trustlife Global Inc. (US) 2026-01-07 EP claimed
EP-4629993-A1 METHODS OF TREATING MYELOPROLIFERATIVE NEOPLASMS Kartos Therapeutics (US) 2025-10-15 EP claimed
US-20250188041-A1 NEW COMPOUNDS AND TREATMENT OF RENAL CELL CARCINOMA Trustlife Global Inc. 2025-06-12 US claimed
CN-119874724-A Novel recruitment element of ubiquitin ligase and application thereof 深圳领济生物科技有限公司 2025-04-25 CN claimed
US-12268681-B2 Methods of treating myeloproliferative neoplasms KARTOS THERAPEUTICS, INC. (US) 2025-04-08 US claimed
US-12215355-B2 Stem cell derived islet differentiation VERTEX PHARMACEUTICALS INCORPORATED (US) 2025-02-04 US claimed
EP-4486348-A1 NEW COMPOUNDS AND TREATMENT OF RENAL CELL CARCINOMA Trustlife Global Inc. (US) 2025-01-08 EP claimed
CN-118804751-A New compounds and treatment of renal cell carcinoma 巴什生物技术公司 2024-10-18 CN claimed
EP-4444870-A1 METHODS AND COMPOSITIONS FOR GENERATING HUMAN ERYTHROID PROGENITOR CELLS Trailhead Biosystems Inc. (US) 2024-10-16 EP claimed
US-20220235327-A1 PANCREATIC DIFFERENTIATION VERTEX PHARMACEUTICALS INCORPORATED 2022-07-28 US claimed
WO-2022072238-A1 TARGETING POLYCYTHEMIA VERA (PV)-INITIATING CELLS BY BLOCKING LEUKOTRIENE BINDING TO THEIR RECEPTORS UNIVERSITY OF MASSACHUSETTS (US) 2022-04-07 WO claimed
WO-2022062356-A1 MEDICINE FOR TREATING OR PREVENTING DISEASES RELATED TO ACTIVITY OF LRRK2 KINASE OR ABNORMAL LRRK2 MUTANT KINASE 广州智睿医药科技有限公司 2022-03-31 WO claimed
US-20220074941-A1 HSP90 COMBINATION THERAPY SLOAN KETTERING INST CANCER RES (US) 2022-03-10 US claimed
US-20210251944-A1 METHODS FOR TREATING A CANCER RESISTANT TO AT LEAST ONE TYROSINE KINASE INHIBITOR DEL MAR PHARMACEUTICALS (BC) LTD. (CA) 2021-08-19 US claimed
CN-112755193-A Method of treating malignancies with anti-tyrosine kinase inhibitors using dianhydrogalactitol or a derivative thereof 德玛医药 2021-05-07 CN claimed
CN-112225703-A Medicine for treating or preventing diseases related to LRRK2 kinase or abnormal LRRK2 mutant kinase activity 广州智睿医药科技有限公司 2021-01-15 CN claimed
EP-2872161-B1 DIANHYDROGALACTITOL FOR USE IN TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS DEL MAR PHARMACEUTICALS (CA) 2020-12-16 EP claimed
US-9238030-B2 Methods for treatment of diseases and disorders related to transducin β-like protein 1 (TBL1) activity, including myeloproliferative neoplasia and chronic myeloid leukemia BETA CAT PHARMACEUTICALS, INC. (US) 2016-01-19 US claimed
CN-104797267-A Method of treating tyrosine kinase inhibitor-resistant malignancies in patients with genetic polymorphism or AHI1 dysregulation or mutation using dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof DEL MAR PHARMACEUTICALS 2015-07-22 CN 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 (5 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-12268681-B2 Methods of treating myeloproliferative neoplasms JAK2, JAK1, PDPK1 BRD4 1177/4885JAK2 1/4885FLT3 78/4885
US-20210251944-A1 METHODS FOR TREATING A CANCER RESISTANT TO AT LEAST ONE TYROSINE KINASE INHIBITOR DCLRE1B, AIPL1, WHR1 BRD4 699/4885JAK2 3633/4885FLT3 2326/4885
US-20220074941-A1 HSP90 COMBINATION THERAPY HSP90AB1, HSP90AB2P, HSP90B1 BRD4 1138/4885JAK2 723/4885FLT3 1684/4885
US-20260097028-A1 Methods of Treating Myeloproliferative Neoplasms JAK2, TP53, CDKN1A BRD4 2054/4885JAK2 1/4885FLT3 171/4885
US-20250188041-A1 NEW COMPOUNDS AND TREATMENT OF RENAL CELL CARCINOMA RCC2, GLS, VHL BRD4 2186/4885JAK2 1549/4885FLT3 1854/4885

“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.