R-406

R-406

SCHEMBL1222514

COc1cc(Nc2ncc(F)c(Nc3ccc4c(n3)NC(=O)C(C)(C)O4)n2)cc(OC)c1OC.O=S(=O)(O)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SYK

The experimentally established mechanism targets of R-406. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SYK known ✓ P43405 13/20 0.83
ADORA3 P0DMS8 2/20 1.00
TYRO3 Q06418 2/20 1.00
PTK2 Q05397 4/20 0.83
PLK4 O00444 3/20 0.83
AURKA O14965 3/20 0.83
RET P07949 3/20 0.83
FLT3 P36888 3/20 0.83
MAPK8 P45983 3/20 0.83
MAPK9 P45984 3/20 0.83
MST1R Q04912 3/20 0.83
IKBKE Q14164 3/20 0.83
KDR P35968 3/20 0.83
EGFR P00533 3/20 0.83
ITK Q08881 3/20 0.83
JAK3 P52333 3/20 0.83
ULK1 O75385 3/20 0.83
STK16 O75716 2/20 0.83
TNK1 Q13470 2/20 0.83
MAP3K11 Q16584 2/20 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
R-406 SCHEMBL30530501 1.00 ADORA3 (1.00) ADORA3TYRO3SYKPTK2PLK4
R-406 SCHEMBL1200144 0.91 SYK (1.00) ADORA3TYRO3SYKPTK2PLK4
R-406 SCHEMBL29358236 0.91 SYK (1.00) ADORA3TYRO3SYKPTK2PLK4
SCHEMBL1383686 0.87 SYK (0.89) ADORA3TYRO3SYKPTK2PLK4
R-406 SCHEMBL12903997 0.87 SYK (0.92) ADORA3TYRO3SYKPTK2PLK4
SCHEMBL2627469 0.86 SYK (0.91) ADORA3TYRO3SYKPTK2PLK4
R-406 SCHEMBL12903982 0.86 SYK (0.91) ADORA3TYRO3SYKPTK2PLK4
R-406 SCHEMBL12904000 0.86 SYK (0.89) ADORA3TYRO3SYKPTK2PLK4
SCHEMBL11937326 0.85 SYK (0.87) ADORA3TYRO3SYKPTK2PLK4
R-406 SCHEMBL12903973 0.84 SYK (0.86) ADORA3TYRO3SYKPTK2PLK4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240115700-A1 CANCER TREATMENT COMBINATIONS UNIV CALIFORNIA (US) 2024-04-11 US disclosed
US-11654193-B2 Cancer treatment combinations THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2023-05-23 US disclosed
CN-111346101-B Application of TAMATINIB in preparation of medicine for treating glioma 中山大学 2023-01-24 CN disclosed
CN-111346096-B Pharmaceutical composition for preventing or treating glioma 中山大学 2022-11-22 CN disclosed
EP-3936141-A2 ANTI-SENESCENCE COMPOUNDS AND USES THEREOF Erasmus University Rotterdam Medical Center (NL) 2022-01-12 EP disclosed
EP-3247375-B1 ANTI-SENESCENCE COMPOUNDS AND USES THEREOF UNIV ERASMUS MED CT ROTTERDAM (NL) 2021-08-04 EP disclosed
US-20210038716-A1 CANCER TREATMENT COMBINATIONS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2021-02-11 US disclosed
US-10688181-B2 Cancer treatment combinations THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2020-06-23 US disclosed
EP-3024489-B1 SALTS OF 2-AMINO-1-HYDROXYETHYL-8-HYDROXYQUINOLIN-2(1H)-ONE DERIVATIVES HAVING BOTH MUSCARINIC RECEPTOR ANTAGONIST AND BETA-2 ADRENERGIC RECEPTOR AGONIST ACTIVITIES ALMIRALL SA (ES) 2020-02-19 EP disclosed
EP-2961407-B1 SALTS OF 2-AMINO-1-HYDROXYETHYL-8-HYDROXYQUINOLIN-2(1H)-ONE DERIVATIVES HAVING BOTH 2 ADRENERGIC RECEPTOR AGONIST AND M3 MUSCARINIC RECEPTOR ANTAGONIST ACTIVITIES ALMIRALL SA (ES) 2018-04-11 EP disclosed
EP-2118100-A1 NEW 3- ([1,2,4] TRIAZOLO [4,3-A] PYRIDIN-7-YL)BENZAMIDE DERIVATIVES Almirall, S.A. (ES) 2009-11-18 EP disclosed
WO-2009132774-A1 NEW SUBSTITUTED INDOLIN-2-ONE DERIVATIVES AND THEIR USE AS P39 MITOGEN-ACTIVATED KINASE INHIBITORS ALMIRALL, S. A. (ES) 2009-11-05 WO disclosed
EP-2113503-A1 New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors Laboratorios Almirall, S.A. (ES) 2009-11-04 EP disclosed
WO-2009124692-A1 NEW SUBSTITUTED SPIRO[CYCLOALKYL-1,3'-INDOL]-2'(1'H)-ONE DERIVATIVES AND THEIR USE AS P38 MITOGEN-ACTIVATED KINASE INHIBITORS. ALMIRALL, S.A. (ES) 2009-10-15 WO disclosed
EP-2108641-A1 New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors Laboratorios Almirall, S.A. (ES) 2009-10-14 EP disclosed
US-20090042891-A1 Pyrazine Derivatives Useful as Adenosine Receptor Antagonists LABORATORIOS ALMIRALL, S.A. (ES) 2009-02-12 US disclosed
WO-2008131922-A1 NEW 4,8-DIPHENYL-POLYAZANAPHTHALENE DERIVATIVES ALMIRALL, S.A. (ES) 2008-11-06 WO disclosed
WO-2008107125-A1 NEW 3-([1,2,4]TRIAZOLO[4,3-A]PYRIDIN-7-YL)BENZAMIDE DERIVATIVES ALMIRALL, S.A. (ES) 2008-09-12 WO disclosed
EP-1922313-A1 PYRAZINE DERIVATIVES USEFUL AS ADENOSINE RECEPTOR ANTAGONISTS Laboratorios Almirall, S.A. (ES) 2008-05-21 EP disclosed
WO-2007017096-A1 PYRAZINE DERIVATIVES USEFUL AS ADENOSINE RECEPTOR ANTAGONISTS LABORATORIOS ALMIRALL, S.A. (ES) 2007-02-15 WO disclosed

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

For each of this compound's patents that has machine-readable text (1 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-20090042891-A1 Pyrazine Derivatives Useful as Adenosine Receptor Antagonists ADORA2B, ADORA2A, ADORA3 SYK 2537/4885ADORA3 3/4885TYRO3 1087/4885

“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.