Cart
sales@molnova.com
5-Bromo-1H-Indole-3-Carboxylic Acid Methyl Ester
CAS No. 773873-77-1
5-Bromo-1H-Indole-3-Carboxylic Acid Methyl Ester( Methyl 5-bromo-1H-indole-3-carboxylate )
Catalog No. M29537 CAS No. 773873-77-1
5-Bromo-1H-Indole-3-Carboxylic Acid Methyl Ester is a marine derived natural products found in Smenospongia sp.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 35 | In Stock |
|
| 5MG | 29 | In Stock |
|
| 10MG | 43 | In Stock |
|
| 25MG | 73 | In Stock |
|
| 50MG | 107 | In Stock |
|
| 100MG | 160 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name5-Bromo-1H-Indole-3-Carboxylic Acid Methyl Ester
-
NoteResearch use only, not for human use.
-
Brief Description5-Bromo-1H-Indole-3-Carboxylic Acid Methyl Ester is a marine derived natural products found in Smenospongia sp.
-
Description5-Bromo-1H-Indole-3-Carboxylic Acid Methyl Ester is a marine derived natural products found in Smenospongia sp.
-
In Vitro——
-
In Vivo——
-
SynonymsMethyl 5-bromo-1H-indole-3-carboxylate
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number773873-77-1
-
Formula Weight254.08
-
Molecular FormulaC10H8BrNO2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(OC)C1=CNC=2C=CC(Br)=CC21
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
CNT2 inhibitor-1
CNT2 inhibitor-1 is a potent inhibitor of concentrative nucleoside transporter 2 (CNT2; IC50: 640 nM for hCNT2).
-
Caudatin-3-O-β-D-glu...
Caudatin-3-O-β-D-glucopyranosyl-(1-4)-8-D-oleandropyranosyl-(1-4)-β-D-cymaropyranosyl-(1-4)-β-D-cymaropyranoside
-
GJ071 oxalate
GJ071 oxalate is a Nonsense suppressor. Nonsense suppressors (NonSups) induce “readthrough”, i.e., the selection of near cognate tRNAs at premature termination codons and insertion of the corresponding amino acid into nascent polypeptide.
