A cell-permeable hexabromocyclohexane compound that interacts with a solvent-accessible pocket near the activation loop of JAK2 and acts as a specific, reversible, and direct inhibitor of JAK2 autophosphorylation (maximal inhibition at 50 µM in BSC-40 cells overexpressing JAK2). Reduces growth hormone-mediated JAK2 activation in γ2A cells that stably express growth hormone receptor and JAK2. Does not block EGFR autophosphorylation in murine fibroblasts.A cell-permeable, specific, reversible, and direct inhibitor of JAK2 autophosphorylation (maximal inhibition at 50 µM in BSC-40 cells overexpressing JAK2 that interacts with a solvent-accessible pocket near the activation loop of JAK2. Reduces growth hormone-mediated JAK2 activation in γ2A cells that stably express growth hormone receptor and JAK2. Does not block EGFR autophosphorylation in murine fibroblasts.
Specifications and Purity: ≥98%
Molecular Formula: C6H6Br6
Molecular Weight: 557.54
PubChem CID: 74603
Isomeric SMILES: C1(C(C(C(C(C1Br)Br)Br)Br)Br)Br
Related Documents: https://aladdin-for-icloud-store.oss-cn-hangzhou.aliyuncs.com/aladdinsci/pdp/sds/1/H276112-SCI_abfadba8b9d70a8cbb849cf66534654f.pdf
- UPC:
- 51131514
- Condition:
- New
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- H276112-25mg
- CAS:
- 1837-91-8
- Product Size:
- 25mg
- Hazard Statement Codes:
- H319:H302
- Precautionary Statement Codes:
- P501:P305+P351+P338:P301+P312:P330:P280:P270:P264
akash.verma@cenmed.com
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