2. Natural Products
  3. Plants Steroids
  4. Liliaceae
  5. Ophiopogon japonicus (L. f.) Ker-Gawl. Paris polyphylla Smith
  6. Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl

Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl 

Cat. No.: HY-N10825
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Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl is a Steroids product that can be isolated from the roots of Ophiopogon japonicus.

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

Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl Chemical Structure

Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl Chemical Structure

CAS No. : 84914-58-9

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Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl Related Antibodies

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Description

Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl is a Steroids product that can be isolated from the roots of Ophiopogon japonicus[1].

Molecular Weight

871.02

Formula

C44H70O17
CAS No.
SMILES

O[C@@]12[C@@]3([C@@]([C@@]4([H])[C@]([C@@]5(C(C[C@H](CC5)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O[C@H]7[C@@H]([C@H]([C@H](CO7)O)O)O)O)O[C@H]8[C@@H]([C@@H]([C@H]([C@@H](O8)C)O)O)O)=CC4)C)([H])CC3)([H])C[C@]1([H])O[C@]9(CC[C@H](CO9)C)[C@H]2C)C
Structure Classification
Initial Source
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
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Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl Related Classifications

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This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
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Help & FAQs
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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.

Keywords:

Glucopyranoside,(3beta,25R)-17-hydroxyspirost-5-en-3-yl84914-58-9OthersInhibitorinhibitorinhibit

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