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Testosterone cypionate
CAS No. 58-20-8
Testosterone cypionate( —— )
Catalog No. M22379 CAS No. 58-20-8
Testosterone cypionate is Anabolic-Androgenic Steroids (AAS) which are synthetic substances that possess functions similar to testosterone.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 35 | In Stock |
|
| 50MG | Get Quote | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameTestosterone cypionate
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NoteResearch use only, not for human use.
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Brief DescriptionTestosterone cypionate is Anabolic-Androgenic Steroids (AAS) which are synthetic substances that possess functions similar to testosterone.
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DescriptionTestosterone cypionate is Anabolic-Androgenic Steroids (AAS) which are synthetic substances that possess functions similar to testosterone.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number58-20-8
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Formula Weight412.61
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Molecular FormulaC27H40O3
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Purity>98% (HPLC)
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Solubility——
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SMILES[H][C@@]12CC[C@H](OC(=O)CCC3CCCC3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Thrombin inhibitor 5
Thrombin inhibitor 5 (compound 385) is a thrombin inhibitor with IC50 values ranging from 0.1 μM to 1 μM, suitable for venous thromboembolism research.
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Butyrospermol
Butyrospermol is a protolimonoid extracted from shea (Euphorbia). As a long-chain fatty acid ester first discovered from natural products, Butyrospermol has antifeedant and antitumor activities.
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Bacterial Sortase Su...
The Staphylococcus aureus transpeptidase Sortase A (SrtA) anchors virulence and colonization-associated surface proteins to the cell wall. SrtA selectively recognizes a C-terminal LPXTG motif. SrtA readily reacts with its native substrate Abz-LPETG-Dap(DNP)-NH2, cleaving it and catalyzing the formation of an amide bond between the carboxyl group of threonine and the amino group of cell-wall crossbridges.
