Phalloidin Peptide
≥90% (HPLC), powder
Manufacturer: Sigma Aldrich
CAS Number: 17466-45-4
Synonym(S): 28-(2,3-dihydroxy-2-methylpropyl)-18-hydroxy-34-(1-hydroxyethyl)-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octazapentacyclo[12.11.11.03,11.04,9.016,20]hexatriaconta-3(11),4,6,8-tetraene-15,21,24,26,29,32,35-heptone
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 MG | P2141-1-MG | In Stock | ₹ 31,327.55 |
P2141 - 1 MG
In Stock
Quantity
1
Base Price: ₹ 31,327.55
GST (18%): ₹ 5,638.959
Total Price: ₹ 36,966.509
product name
Phalloidin from Amanita phalloides, ≥90%
biological source
Amanita phalloides
Quality Level
200
Assay
≥90%
form
powder
SMILES string
CC(O)C1NC(=O)C(C)NC(=O)C(CC(C)(O)CO)NC(=O)C2Cc3c(SCC(NC1=O)C(=O)N4CC(O)CC4C(=O)NC(C)C(=O)N2)[nH]c5ccccc35
InChI
1S/C35H48N8O11S/c1-15-27(47)38-22-10-20-19-7-5-6-8-21(19)41-33(20)55-13-24(34(53)43-12-18(46)9-25(43)31(51)37-15)40-32(52)26(17(3)45)42-28(48)16(2)36-30(50)23(39-29(22)49)11-35(4,54)14-44/h5-8,15-18,22-26,41,44-46,54H,9-14H2,1-4H3,(H,36,50)(H,37,51)(H,38,47)(H,39,49)(H,40,52)(H,42,48)
InChI key
KPKZJLCSROULON-UHFFFAOYSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Cayman Chemical Phalloidin, 17466-45-4, 1 mg | -- | ₹ 21,646.68 | |
| | Medchemexpress LLC HY-P0028 1mg Medchemexpress, Phalloidin CAS:17466-45-4 Purity:>98% | -- | ₹ 40,427.10 | |
| | Sigma Aldrich Fine Chemicals Biosciences Phalloidin from Amanita phalloides >=90% | 17466-45-4 | MFCD03427567 | 1MG | -- | ₹ 32,596.65 | |
| | 17466-45-4 | Phalloidin | -- | ₹ 16,940.88 |
Related Products
Description
- General description: Phalloidin is a phallotoxin produced by death cap mushroom Amanita phalloides. It is a cyclic peptide, which interacts with actin, and this was first identified in phalloidin-poisoned rats. It is a heptapeptide, cyclic in nature, with a crosslink between tryptophan at position 6 and cysteine at position 3.[1] The side chain of amino acid 7 (γ-δ-dihydroxyleucine) in phalloidin, is accessible to modifications, through which fluorescently labeled phalloidin compounds can be produced.[2]
- Application: Phalloidin has been used: As a supplement in PEM buffer and dimethyl sulfoxide (DMSO).[3]As a drug.[4]In immunohistochemistry to stain F-actin.[5]
- Biochem/physiol Actions: Phalloidin interacts with polymeric actin, and not oligomeric or monomeric forms. This interaction leads to highly stabilized actin filaments, which resist depolymerization and disassembly. In rats, this toxin causes death due to liver hemorrhage and cells show abnormal actin clustering.[1] The affinity of phalloidin to actin is not significantly altered after derivatizing fluorescently labelled phalloidin compounds. These compounds can be used to study actin structure and organization within eukaryotic cells.[2]
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
P260 - P262 - P264 - P280 - P302 + P352 + P310 - P304 + P340 + P310
Hazard Classifications
Acute Tox. 2 Oral
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable