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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Phalloidin

OCC(CC1NC(=O)C2NC(=O)C(C)NC(=O)C3CC(CN3C(=O)C(CSc3c(C2)c2ccccc2[nH]3)NC(=O)C(NC(=O)C(NC1=O)C)C(O)C)O)(O)C Request for Quotation
Chemical Name: Phalloidin
CAS Number: 17466-45-4
Product Number: AG00AP3E(AGN-PC-0713M8)
Synonyms:
MDL No: MFCD03427567
Molecular Formula: C35H48N8O11S
Molecular Weight: 788.8676

Identification/Properties

Computed Properties
Molecular Weight:
788.874g/mol
XLogP3:
-1.7
Hydrogen Bond Donor Count:
11
Hydrogen Bond Acceptor Count:
12
Rotatable Bond Count:
4
Exact Mass:
788.316g/mol
Monoisotopic Mass:
788.316g/mol
Topological Polar Surface Area:
317A^2
Heavy Atom Count:
55
Formal Charge:
0
Complexity:
1510
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
10
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phalloidin is a naturally occurring compound that has found significant application in chemical synthesis, particularly in the field of bioconjugation and drug development. As a potent actin-binding molecule, Phalloidin offers a valuable tool for anchoring fluorescent dyes or other biomolecules to actin filaments, allowing for their visualization and study within biological systems. In chemical synthesis, Phalloidin serves as a versatile linker molecule for creating new conjugates with specific targeting capabilities, enabling the development of novel therapeutics or research tools. Its ability to selectively bind to actin filaments makes Phalloidin a valuable asset in designing drug delivery systems or molecular probes for studying cellular processes. By harnessing the unique properties of Phalloidin, researchers can enhance the precision and efficiency of their synthetic endeavors, opening up new possibilities for advancing various scientific and medical applications.