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Substance P 1-7
CAS No. 68060-49-1
Substance P 1-7 ( —— )
Catalog No. M20901 CAS No. 68060-49-1
Substance P 1-7 is the major bioactive metabolite formed after proteolytic degradation of the tachykinin substance P (SP)with anti-inflammatory anti-nociceptive and anti-hyperalgesic effects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 63 | In Stock |
|
| 5MG | 88 | In Stock |
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| 10MG | 144 | In Stock |
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| 25MG | 259 | In Stock |
|
| 50MG | 389 | In Stock |
|
| 100MG | 583 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameSubstance P 1-7
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NoteResearch use only not for human use.
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Brief DescriptionSubstance P 1-7 is the major bioactive metabolite formed after proteolytic degradation of the tachykinin substance P (SP)with anti-inflammatory anti-nociceptive and anti-hyperalgesic effects.
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DescriptionSubstance P 1-7 is the major bioactive metabolite formed after proteolytic degradation of the tachykinin substance P (SP)with anti-inflammatory anti-nociceptive and anti-hyperalgesic effects.
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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 Number68060-49-1
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Formula Weight900.04
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Molecular FormulaC41H65N13O10
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Purity>98% (HPLC)
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Solubility——
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SMILESN=C(N)NCCCC(N)C(=O)N1CCCC1C(=O)NC(CCCCN)C(=O)N1CCCC1C(=O)NC(CCC(N)=O)C(=O)NC(CCC(N)=O)C(=O)NC(Cc1ccccc1)C(=O)O
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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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Mangiferin
Mangiferin is used for antidiabetes. Extracted from Mangifera indica L.
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Pyrimidine
Pyrimidines are heterocyclic six-membered nitrogen-containing carbon ring structures with uracil cytosine and thymine being the basal structures of ribose-containing nucleosides (uridine cytidine and thymidine respectively) or deoxyribose-containing deoxynucleosides and their corresponding ribonucleotides or deoxyribonucleotides.
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ShK-Dap22
Extremely potent KV1.3 channel blocker (Kd = 23 pM for mKV1.3 currents). Selective for KV1.3 over other mammalian potassium channels (IC50 values are 23, 1800, 10500, 37000 and 39000 pM for mKV1.3, mKV1.1, hKV1.6, mKV1.4 and rKV1.2 respectively, and >100000 pM for hKV1.5, mKV1.7, hKV3.1, rKV3.4 and hKCa4). Suppresses T cell activation in vitro (IC50 < 500 pM).
