Calyculin A

Modify Date: 2025-08-27 16:02:55

Calyculin A Structure
Calyculin A structure
Common Name Calyculin A
CAS Number 101932-71-2 Molecular Weight 1009.17000
Density 1.25g/cm3 Boiling Point N/A
Molecular Formula C50H81N4O15P Melting Point N/A
MSDS Chinese USA Flash Point N/A
Symbol GHS06
GHS06
Signal Word Danger

 Use of Calyculin A


Calyculin A is a potent and cell-permeable protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) inhibitor with IC50s of 0.5 to 1 nM.

 Names

Name Calyculin A from Discodermia calyx
Synonym More Synonyms

 Calyculin A Biological Activity

Description Calyculin A is a potent and cell-permeable protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) inhibitor with IC50s of 0.5 to 1 nM.
Related Catalog
References

[1]. Ishihara H, et al. Calyculin A and okadaic acid: inhibitors of protein phosphatase activity. Biochem Biophys Res Commun. 1989 Mar 31;159(3):871-7.

 Chemical & Physical Properties

Density 1.25g/cm3
Molecular Formula C50H81N4O15P
Molecular Weight 1009.17000
Exact Mass 1008.54000
PSA 296.80000
LogP 5.07988
Index of Refraction 1.57
Storage condition 2-8℃

 Safety Information

Symbol GHS06
GHS06
Signal Word Danger
Hazard Statements H301 + H311 + H331-H315
Precautionary Statements P261-P280-P301 + P310-P311
Personal Protective Equipment Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges
Hazard Codes T: Toxic;
Risk Phrases 23/24/25-38
Safety Phrases 36/37/39-45
RIDADR UN 3462 6.1/PG 3
Packaging Group II
Hazard Class 6.1(a)

 Articles35

More Articles
A novel receptor cross-talk between the ATP receptor P2Y2 and formyl peptide receptors reactivates desensitized neutrophils to produce superoxide

Exp. Cell Res. 323(1) , 209-17, (2014)

Neutrophils express several G-protein coupled receptors (GPCRs) and they cross regulate each other. We described a novel cross-talk mechanism in neutrophils, by which signals generated by the receptor...

Detachment-induced autophagy in three-dimensional epithelial cell cultures.

Meth. Enzymol. 452 , 423-39, (2009)

Integrin-mediated cell adhesion to extracellular matrix (ECM) is critical for normal epithelial cell survival; cells deprived of ECM contact rapidly undergo apoptotic cell death, termed anoikis. Recen...

Unique features of the okadaic acid activity class of tumor promoters.

J. Cancer Res. Clin. Oncol. 125 , 150-155, (1999)

Following the first report of tumor promotion by okadaic acid in 1988, we further identified additional tumor promoters of the okadaic acid activity class, such as calyculin A and microcystin-LR. Howe...

 Synonyms

Calyculin A,N-[(3S)-[4-(1E)-3-[(2R,3R,4R,7S,8S,9R)-2-[(1S,3S,4S,5R,7E,9E,11E,13Z)-14-Cyano-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyl-7,9,11,13-tetradecatetraenyl]-9-hydroxy-4,4,8-trimethyl-3-(phosphonooxy)-1,6-dioxaspiro[4.5]dec-7-yl]-1-propenyl]-2-o
MFCD00133156
Calyculin A
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here



Get all suppliers and price by the below link:

Calyculin A suppliers


Price: $96/0.5mM*20uLinDMSO

Reference only. check more Calyculin A price

Related Compounds: More...
actinoplanone A
115655-86-2
Thapsuine A
76429-00-0
Apocynol A
358721-33-2
(2S)-N-[(2S,5S,8S,11R,12S,15S,18S,21R)-5-[(3-bromo-4-methoxyphenyl)methyl]-2-[(2S)-butan-2-yl]-15-[3-(carbamoylamino)propyl]-21-hydroxy-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-8-propan-2-yl-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]-2-(butanoyla
1007391-44-7
Pseudoanguillosporin A
1159392-22-9
Digitoside A
140208-79-3
Tirandamycin A
34429-70-4
Blattellastanoside A
149864-63-1
amaronol a
226560-96-9
1-[N-methyl3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclobutaneamido]cyclopropane-1-carboxylic acid
2171160-99-7
rac-1-[N-methyl(1R,2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cycloheptaneamido]cyclopropane-1-carboxylic acid
2227853-53-2
1-[3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-N-methylpropanamido]cyclopropane-1-carboxylic acid
2171555-83-0
1-{3-[benzyl(methyl)amino]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-N-methylpropanamido}cyclopropane-1-carboxylic acid
2171763-18-9
(2R,3S)-3-(benzyloxy)-2-{[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cycloheptyl]formamido}butanoic acid
2648929-73-9
(2R,3S)-3-(benzyloxy)-2-{2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)piperidin-1-yl]acetamido}butanoic acid
2171168-50-4
(2R,3S)-3-(benzyloxy)-2-[(3S)-3-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-5-methylhexanamido]butanoic acid
2171161-06-9
(2R,3S)-3-(benzyloxy)-2-[6-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylheptanamido]butanoic acid
2648935-15-1
(2R,3S)-3-(benzyloxy)-2-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-5,5-dimethylhexanamido]butanoic acid
2648918-58-3
(2R,3S)-3-(benzyloxy)-2-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-4,4-dimethylpentanamido}butanoic acid
2648931-96-6