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133413-70-4,MFCD00894026
Catalog No.:AA0080F3

133413-70-4 | Pf-1022a

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$173.00   $121.00
- +
5mg
≥98%
in stock  
$688.00   $481.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0080F3
Chemical Name:
Pf-1022a
CAS Number:
133413-70-4
Molecular Formula:
C52H76N4O12
Molecular Weight:
949.1794
MDL Number:
MFCD00894026
SMILES:
CC(C[C@H]1C(=O)O[C@H](Cc2ccccc2)C(=O)N(C)[C@@H](CC(C)C)C(=O)O[C@H](C)C(=O)N(C)[C@H](C(=O)O[C@@H](C(=O)N([C@H](C(=O)O[C@@H](C(=O)N1C)C)CC(C)C)C)Cc1ccccc1)CC(C)C)C
Properties
Computed Properties
 
Complexity:
1580  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
8  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
68  
Hydrogen Bond Acceptor Count:
12  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
12  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
9.5  

Literature

Title: Anthelmintic cyclcooctadepsipeptides: complex in structure and mode of action.

Journal: Trends in parasitology 20120901

Title: Efficacy of the cyclooctadepsipeptide PF1022A against Heligmosomoides bakeri in vitro and in vivo.

Journal: Parasitology 20110801

Title: Effects of the anthelmintic drug PF1022A on mammalian tissue and cells.

Journal: Biochemical pharmacology 20090415

Title: In vitro synthesis of new cyclodepsipeptides of the PF1022-type: probing the alpha-D-hydroxy acid tolerance of PF1022 synthetase.

Journal: Chembiochem : a European journal of chemical biology 20090126

Title: Influence of the cyclooctadepsipeptides PF1022A and PF1022E as natural products on the design of semi-synthetic anthelmintics such as emodepside.

Journal: Parasitology research 20051001

Title: Efficacy of two cyclooctadepsipeptides, PF1022A and emodepside, against anthelmintic-resistant nematodes in sheep and cattle.

Journal: Parasitology 20050301

Title: Para-position derivatives of fungal anthelmintic cyclodepsipeptides engineered with Streptomyces venezuelae antibiotic biosynthetic genes.

Journal: Nature biotechnology 20040701

Title: Cyclooctadepsipeptides--an anthelmintically active class of compounds exhibiting a novel mode of action.

Journal: International journal of antimicrobial agents 20030901

Title: Restricted conformation analogues of an anthelmintic cyclodepsipeptide.

Journal: Journal of medicinal chemistry 20030522

Title: Synthesis of anthelmintically active N-methylated amidoxime analogues of the cyclic octadepsipeptide PF1022A.

Journal: Pest management science 20021201

Title: Cyclooctadepsipeptides--a new class of anthelmintically active compounds.

Journal: Parasitology research 20020601

Title: Generation of a small library of cyclodepsipeptide PF1022A analogues using a cyclization-cleavage method with oxime resin.

Journal: Bioorganic & medicinal chemistry letters 20020211

Title: Synthesis and anthelmintic activity of thioamide analogues of cyclic octadepsipeptides such as PF1022A.

Journal: Pest management science 20011101

Title: Dornetshuber R, et al. Effects of the anthelmintic drug PF1022A on mammalian tissue and cells. Biochem Pharmacol. 2009 Apr 15;77(8):1437-44.

Title: Sasaki T, et al. A new anthelmintic cyclodepsipeptide, PF1022A. J Antibiot (Tokyo). 1992 May;45(5):692-7.

Title: Nwosu U, et al. Efficacy of the cyclooctadepsipeptide PF1022A against Heligmosomoides bakeri in vitro and in vivo. Parasitology. 2011 Aug;138(9):1193-201.

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Tags:133413-70-4 Molecular Formula|133413-70-4 MDL|133413-70-4 SMILES|133413-70-4 Pf-1022a
Catalog No.: AA0080F3
133413-70-4,MFCD00894026
133413-70-4 | Pf-1022a
Pack Size： 1mg
Purity： ≥98%
in stock
$173.00 $121.00
Pack Size： 5mg
Purity： ≥98%
in stock
$688.00 $481.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0080F3
Chemical Name: Pf-1022a
CAS Number: 133413-70-4
Molecular Formula: C52H76N4O12
Molecular Weight: 949.1794
MDL Number: MFCD00894026
SMILES: CC(C[C@H]1C(=O)O[C@H](Cc2ccccc2)C(=O)N(C)[C@@H](CC(C)C)C(=O)O[C@H](C)C(=O)N(C)[C@H](C(=O)O[C@@H](C(=O)N([C@H](C(=O)O[C@@H](C(=O)N1C)C)CC(C)C)C)Cc1ccccc1)CC(C)C)C
Properties
Complexity: 1580  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 8  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 68  
Hydrogen Bond Acceptor Count: 12  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 12  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 9.5  
Literature fold

Title: Anthelmintic cyclcooctadepsipeptides: complex in structure and mode of action.

Journal: Trends in parasitology20120901

Title: Efficacy of the cyclooctadepsipeptide PF1022A against Heligmosomoides bakeri in vitro and in vivo.

Journal: Parasitology20110801

Title: Effects of the anthelmintic drug PF1022A on mammalian tissue and cells.

Journal: Biochemical pharmacology20090415

Title: In vitro synthesis of new cyclodepsipeptides of the PF1022-type: probing the alpha-D-hydroxy acid tolerance of PF1022 synthetase.

Journal: Chembiochem : a European journal of chemical biology20090126

Title: Influence of the cyclooctadepsipeptides PF1022A and PF1022E as natural products on the design of semi-synthetic anthelmintics such as emodepside.

Journal: Parasitology research20051001

Title: Efficacy of two cyclooctadepsipeptides, PF1022A and emodepside, against anthelmintic-resistant nematodes in sheep and cattle.

Journal: Parasitology20050301

Title: Para-position derivatives of fungal anthelmintic cyclodepsipeptides engineered with Streptomyces venezuelae antibiotic biosynthetic genes.

Journal: Nature biotechnology20040701

Title: Cyclooctadepsipeptides--an anthelmintically active class of compounds exhibiting a novel mode of action.

Journal: International journal of antimicrobial agents20030901

Title: Restricted conformation analogues of an anthelmintic cyclodepsipeptide.

Journal: Journal of medicinal chemistry20030522

Title: Synthesis of anthelmintically active N-methylated amidoxime analogues of the cyclic octadepsipeptide PF1022A.

Journal: Pest management science20021201

Title: Cyclooctadepsipeptides--a new class of anthelmintically active compounds.

Journal: Parasitology research20020601

Title: Generation of a small library of cyclodepsipeptide PF1022A analogues using a cyclization-cleavage method with oxime resin.

Journal: Bioorganic & medicinal chemistry letters20020211

Title: Synthesis and anthelmintic activity of thioamide analogues of cyclic octadepsipeptides such as PF1022A.

Journal: Pest management science20011101

Title: Dornetshuber R, et al. Effects of the anthelmintic drug PF1022A on mammalian tissue and cells. Biochem Pharmacol. 2009 Apr 15;77(8):1437-44.

Title: Sasaki T, et al. A new anthelmintic cyclodepsipeptide, PF1022A. J Antibiot (Tokyo). 1992 May;45(5):692-7.

Title: Nwosu U, et al. Efficacy of the cyclooctadepsipeptide PF1022A against Heligmosomoides bakeri in vitro and in vivo. Parasitology. 2011 Aug;138(9):1193-201.

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