Hirudin (54-65) (desulfated)
CAS No. 113274-56-9
Hirudin (54-65) (desulfated) ( ——— )
Catalog No. M39955 CAS No. 113274-56-9
Hirudin (54-65) is a fragment of the 65 residue protein of Hirudin with anticoagulant effects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 449 | In Stock |
|
| 10MG | 655 | In Stock |
|
| 25MG | 1026 | In Stock |
|
| 50MG | 1358 | In Stock |
|
| 100MG | 1832 | In Stock |
|
| 200MG | 2474 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameHirudin (54-65) (desulfated)
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NoteResearch use only, not for human use.
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Brief DescriptionHirudin (54-65) is a fragment of the 65 residue protein of Hirudin with anticoagulant effects.
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DescriptionHirudin (54-65) is a fragment of the 65 residue protein of Hirudin with anticoagulant effects.
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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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Recptor———
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Research Area———
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Indication———
Chemical Information
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CAS Number113274-56-9
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Formula Weight1468.52
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Molecular FormulaC66H93N13O25
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Purity>98% (HPLC)
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Solubility———
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SMILESC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC1=CC=CC=C1)NC([C@@H](NC(CN)=O)CC(O)=O)=O)=O)CCC(O)=O)=O)CCC(O)=O)=O)[C@H](CC)C)(=O)N2[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CC3=CC=C(O)C=C3)C(N[C@H](C(N[C@@H](CCC(N)=O)C(O)=O)=O)CC(C)C)=O)=O)CCC(O)=O)=O)CCC(O)=O)=O)CCC2
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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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Stichodactyla helian...
ShK toxin blocks voltage-dependent potassium channel (Kv1.3 channel). ShK toxin can be isolated from the whole body extract of the Caribbean sea anemone (Stichodactylu helianthus). ShK toxin competes with dendrotoxin I and α-dendrotoxin for binding to synaptosomal membranes of rat brain, facilitates acetylcholine release. ShK toxin suppresses K+ currents in cultured rat dorsal root ganglion neurons. ShK toxin also inhibits T lymphocyte proliferation.
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α1 adrenoceptor-MO-1
α1 adrenoceptor-MO-1 (S enantiomer) has affinity at alpha 1 adrenergic receptor with alphalytic activity and analgesic action. It has more active than R enantiomer.
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