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Merck

580551

Tautomycin, Streptomyces spiroverticillatus

Tautomycin, CAS 109946-35-2, is a potent inhibitor of protein phosphatase 1, 2A, and smooth muscle endogenous phosphatase (IC50 = 1 nM, 10 nM, and 6 nM, respectively). Mixture of two isomers.

Synonym(s):

Tautomycin, Streptomyces spiroverticillatus

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About This Item

Empirical Formula (Hill Notation):
C41H66O13
CAS Number:
109946-35-2
Molecular Weight:
766.95
UNSPSC Code:
12352200
Assay:
≥97% (HPLC)
Form:
lyophilized (thin film)
Quality level:
100
Storage condition:
OK to freeze, desiccated, protect from light

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InChI key

RFCWHQNNCOJYTR-IRCAEPKSSA-N

InChI

1S/C41H66O13/c1-21(2)36(51-34(47)20-31(45)35-27(8)39(48)52-40(35)49)38(50-10)32(46)19-30(44)26(7)29(43)13-11-24(5)37-25(6)16-18-41(54-37)17-15-23(4)33(53-41)14-12-22(3)28(9)42/h21-26,29,31-33,36-38,43,45-46H,11-20H2,1-10H3/t22-,23+,24+,25-,26-,29-,31+,32+,33-,36+,37-,38+,41+/m0/s1

assay

≥97% (HPLC)

form

lyophilized (thin film)

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, desiccated, protect from light

solubility

chloroform: soluble, ethanol: soluble, methanol: soluble

shipped in

ambient

storage temp.

−20°C

Quality Level

100

General description

Mixture of two isomers. Potent inhibitor of protein phosphatases and useful for studies involving protein phosphorylation. Inhibits protein phosphatase 1 (IC50 = 1 nM), protein phosphatase 2A (IC50 = 10 nM), and smooth muscle endogenous phosphatase (IC50 = 6 nM). Higher concentrations are needed to inhibit protein phosphatase 2B. Does not inhibit protein phosphatase 2C or phorbol dibutyrate binding. Does not activate protein kinase C or inhibit myosin light chain kinase.

Biochem/physiol Actions

Cell permeable: no
Primary Target
PP1
Product does not compete with ATP.
Reversible: no
Target IC50: 1 nM, 10 nM, 6 nM, against protein phosphatase 1, protein phosphatase 2A, and smooth muscle endogenous phosphatase, respectively

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.







From Catalog:

Desc. Field- removed ". . .and useful for studies involving protein phosphorylation"

- removed ". . .or phorbol dibutyrate binding. Does not activate protein kinase C or inhibit myosin light chain kinase"

Other Notes

Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
McCluskey, A., et al. 2002. J. Med. Chem.45, 1151.
Mitsuhashi, S., et al. 2001. Biochem. Biophys. Res. Commun.287, 328.
Kikuchi, K., et al. 1999. Int. J. Mol. Med.4, 395.
Sheppeck, J.E., et al. 1997. J. Org. Chem.62, 387.
Sugiyama, Y., et al. 1996. Bioorg. Med. Chem. Lett.6, 3.
Gong, M.C., et al. 1992. J. Biol. Chem.267, 14662.
Suganuma, M., et al. 1992. Toxicon30, 873.
MacKintosh, C. and Klumpp, S. 1990. FEBS Lett.277, 137.
Magae, J., et al. 1989. J. Antibiot.42, 1290.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Highly Toxic (H)

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H300

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

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