9H-Carbazole, 1-methyl-
CAS No. 6510-65-2
9H-Carbazole, 1-methyl-( -Methyl-9H-carbazole | 1-Methyl-carbazole | 1-methyl carbazole )
Catalog No. M29564 CAS No. 6510-65-2
9H-Carbazole, 1-methyl- is a marine derived natural products found in Tedania (Tedania) ignis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 32 | In Stock |
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| 5MG | 29 | In Stock |
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| 10MG | 43 | In Stock |
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| 25MG | 73 | In Stock |
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| 50MG | 107 | In Stock |
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| 100MG | 160 | In Stock |
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| 200MG | 241 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name9H-Carbazole, 1-methyl-
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NoteResearch use only, not for human use.
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Brief Description9H-Carbazole, 1-methyl- is a marine derived natural products found in Tedania (Tedania) ignis.
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Description9H-Carbazole, 1-methyl- is a marine derived natural products found in Tedania (Tedania) ignis.
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In Vitro——
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In Vivo——
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Synonyms-Methyl-9H-carbazole | 1-Methyl-carbazole | 1-methyl carbazole
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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 Number6510-65-2
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Formula Weight181.23
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Molecular FormulaC13H11N
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Purity>98% (HPLC)
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Solubility——
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SMILESC=1C=CC2=C(C1)NC3=C2C=CC=C3C
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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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PAR-3 (1-6) amide (m...
SFNGGP-NH2 is a biological active peptide. (PAR-3 is a high-affinity thrombin receptor. PAR-3 mRNA is expressed in the cutaneous mast cells of humans. Protease-Activated Receptors (PARs) have been studied for their roles in itch and their itch-associated response through histamine-dependent/independent pathways have been reported. PAR-3 has been shown not to induce itching alone but possibly in conjunction with PAR-4. Co-expression of PAR-3 and PAR-4 enhances thrombin action suggesting that PAR-3 alone does not mediate transmembrane signaling but instead functions as a cofactor to activate PAR-4.)
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Retrorsine
Retrorsine is a naturally occurring toxic pyrrolizidine alkaloid. Retrorsine can bind with DNA and inhibits the proliferative capacity of hepatocytes.
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NU 9056
NU 9056 is an effective and selective inhibitor of KAT5 histone acetyltransferase with an IC50 of 2 μM. NU 9056 blocks DNA damage response and inhibits protein acetylation in prostate cancer cell lines.
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