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Cat. No.: HY-116939

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(E)-Broparestrol

(E)-Broparestrol is a biologically active tetrasubstituted olefin, which is used as an estrogen in dermatology.

For research use only. We do not sell to patients.

CAS No.: 22393-62-0
Formula: C₂₂H₁₉Br
Molecular Weight:363.29

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (269 KB)

(E)-Broparestrol Chemical Structure

CAS No.: 22393-62-0

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity

Description

(E)-Broparestrol is a biologically active tetrasubstituted olefin, which is used as an estrogen in dermatology^[1].

All Estrogen Receptor/ERR Isoforms :

Chemical Information

CAS No. 22393-62-0
Molecular Weight 363.29
Formula C₂₂H₁₉Br
SMILES

CCC1=CC=C(C=C1)/C(C2=CC=CC=C2)=C(C3=CC=CC=C3)/Br
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Protocols

All Signal Pathway Related

Research Protocol for Endocrine Diseases
Endocrine diseases often arise from disrupted hormone production, hormone signaling, or target-tissue responsiveness; for diabetes-focused endocrine disease models, insulin signaling regulates glucose uptake, hepatic glucose output, lipid metabolism, and β-cell compensation. Type 2 diabetes develops through interacting defects in insulin resistance, β-cell dysfunction, adipose inflammation, hepatic glucose overproduction, altered incretin signaling, and ectopic lipid metabolism. A major unresolved question is whether endocrine dysfunction is driven primarily by target-tissue insulin resistance, intrinsic β-cell failure, immune/inflammatory stress, or combined multi-organ failure that differs by disease stage.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (269 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Al-Hassan M I. Synthesis of broparestrol using palladium-catalyzed cross-coupling[J]. Journal of organometallic chemistry, 1987, 321(1): 119-121.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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