1. Metabolic Enzyme/Protease
  2. Endogenous Metabolite
  3. Sarcophine

Sarcophine ((+)-Sarcophine) is a potent glycine receptor (GlyR) inhibitor with an IC50 value of 3.9 μM. Sarcophine is a nature product that could be isolated form the Red Sea soft coral Sarcophyton glaucum.

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

Sarcophine Chemical Structure

Sarcophine Chemical Structure

CAS No. : 55038-27-2

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Description

Sarcophine ((+)-Sarcophine) is a potent glycine receptor (GlyR) inhibitor with an IC50 value of 3.9 μM. Sarcophine is a nature product that could be isolated form the Red Sea soft coral Sarcophyton glaucum[1].

In Vitro

Sarcophine ((+)-Sarcophine) is an inhibitor of recombinant glycine receptors, with a Ki value of 2.1 μM[1].
Sarcophine (1-100 mM; 24 h) has cytotoxicity against HEK293 cells with an LD50 value of 29.3 mM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

316.43

Formula

C20H28O3

CAS No.
SMILES

O=C1C(C)=C2[C@](O1)([H])/C=C(C)/CC[C@H]3[C@](O3)(C)CC/C=C(C)/CC2

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
References
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Sarcophine Related Classifications

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Sarcophine
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HY-124550
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