EGF-06335 Red

CCOC(=O)Cc1csc(=NN=C(C)c2ccc(N(C)C)cc2)[nH]1
0.338
Platform Score
2D Structure
EGF-06335
C17H22N4O2S | Exact mass: 346.1463
Key Metrics
N/A
Vina (kcal/mol)
#-
Docking Rank
0
Hinge Binder
70
TPSA
346
MW
1
HBD
2.6
SlogP
Display Controls





EGFR Docking Result
N/A
kcal/mol (molecular docking)
Docking Rank#- of 1,249
Consensus Score-
ReceptorEGFR (PDB: 1M17)
Selective No
Selectivity Profile
ADMET Profile
BBB (BOILED-Egg) BBB- (non-penetrant)
ADMET Status Pass (no hard fails)
CNS Drug-Likeness
Physicochemical Properties
Molecular Weight346.50 Da
TPSA70.0 A^2
HBD1
HBA6
SlogP2.57
Fsp30.353
Rotatable Bonds6
Rings2 (2 aromatic)
QED0.496
SA Score3.01 (1=easy, 10=hard)
CNS MPO- / 4.0
FormulaC17H22N4O2S
Exact Mass346.1463
Classification
Scaffold (Murcko)-
Source Versions-
Best Source Score-
Best Source Rank#-
Hinge Binder Not present
InChIKey-
Filter PassYes
Retrosynthetic Analysis

Retrosynthetic analysis not yet run for this compound.

About

Retrosynthetic analysis decomposes the target molecule into purchasable building blocks using learned reaction templates.

A feasible route means the molecule can theoretically be synthesized from commercially available starting materials.

Min steps indicates the shortest synthesis route found.

Matched Molecular Pair Analysis

Find structural transformations that improve BBB penetration by analyzing pairs of similar molecules with different predictions.

About MMP

Matched Molecular Pairs (MMPs) are pairs of molecules that differ by a single structural transformation.

By comparing BBB predictions across many such pairs, we identify systematic SAR rules — specific modifications that consistently improve or reduce BBB penetration.

Suggestions are based on transformations observed in similar molecules within the compound library.

Patent Landscape Screening

Screen this compound against global patent databases (SureChEMBL + PubChem).

About IP Screening

Searches performed:

  • Exact structure match (SureChEMBL)
  • Substructure / Markush coverage
  • Similarity search (70% Tanimoto)
  • PubChem patent annotations

Risk levels:

  • CRITICAL Exact match in active patent
  • HIGH Substructure / Markush hit
  • MODERATE High similarity (>85%)
  • LOW Moderate similarity
  • CLEAR No hits found
Disclaimer: This is a computational screening tool only. It does not constitute legal advice. 18-month publication lag means recent filings may not appear. Consult qualified IP counsel for formal FTO opinions.