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Benzoxazolines

Organic heterocyclic compounds that consist of benzene fused with an oxazolines; oxazolines are a five-membered ring with three carbon atoms, one oxygen atom, and one nitrogen atom.

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1

eMolecules​ 3,4-Dihydro-2h-1,4-benzoxazine-2-carboxylic acid | 90563-93-2 | MFCD05865108 | 1g

Combi-Blocks, Inc. | 3,4-Dihydro-2h-1,4-benzoxazine-2-carboxylic acid | 1g | 603139684 | QK-4942 | 98.000 | 90563-93-2 | MFCD05865108 | 179.175 | C9H9NO3

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2

eMolecules​ 3,4-Dihydro-2h-1,4-benzoxazine-2-carboxylic acid hydrochloride | 90563-93-2 | MFCD08310679 | 1g

Combi-Blocks | 3,4-Dihydro-2h-1,4-benzoxazine-2-carboxylic acid hydrochloride | 1g | 448005718 | QW-1182 | 98.000 | 90563-93-2 | MFCD08310679 | 215.630 | C9H10ClNO3

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3

eMolecules​ (6-Bromo-2-oxo-1,3-benzoxazol-3(2H)-yl)acetic acid | 100219-71-4 | MFCD00700893 | 1g

Combi-Blocks, Inc. | (6-Bromo-2-oxo-1,3-benzoxazol-3(2H)-yl)acetic acid | 1g | 603140670 | QY-2472 | 95.000 | 100219-71-4 | MFCD00700893 | 272.054 | C9H6BrNO4

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4

Medchemexpress LLC Protac pan-AKT degrader (ipatasertib-lenalidomide conjugate) | 2503017-97-6 | 99.7% | 798.41 g·mol⁻¹ | C44H56ClN7O5 | 5 MG
SDP

A potent, selective PROTAC-based pan-AKT degrader that links an ATP-competitive AKT inhibitor to a cereblon ligand to induce degradation of AKT1, AKT2, and AKT3. It is supplied as a white to off-white solid for research use in biochemical and cellular studies of AKT signaling and degradation mechanisms.

  • Potent degradation of AKT isoforms with low-nanomolar activity.
  • High chemical purity (≈99.7%).
  • Molecular weight 798.41 g·mol⁻¹ and formula C44H56ClN7O5.
  • White to off-white solid form.
  • Storage: sealed, away from moisture; in solvent -80°C up to 6 months, -20°C up to 1 month.
  • Suitable for biochemical and cellular AKT pathway studies.

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