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ROTTLERIN

CAS No.
82-08-6
Chemical Name:
ROTTLERIN
Synonyms
MALLOTOXIN;kamalin;NSC 94525;NSC 56346;ROTTLERIN;Rottierin;Rottlerin,98%;Rottlerin, 98% 10MG;Rottlerin (Mallotoxin;4’,6’-trihydroxy-5’-methyl-methyl)-2
CBNumber:
CB4260488
Molecular Formula:
C30H28O8
Molecular Weight:
516.54
MDL Number:
MFCD00017361
MOL File:
82-08-6.mol
Last updated:2023-06-30 15:45:59

ROTTLERIN Properties

Melting point 200 °C
Boiling point 521.39°C (rough estimate)
Density 1.2051 (rough estimate)
refractive index 1.4900 (estimate)
storage temp. 2-8°C
solubility Soluble in DMSO (up to 50 mg/ml).
form Powder
pka 6.92±0.40(Predicted)
color Orange to brown
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 1 month.
LogP 8.660 (est)
CAS DataBase Reference 82-08-6(CAS DataBase Reference)
FDA UNII E29LP3ZMUH

SAFETY

Risk and Safety Statements

Hazard Codes  Xn
Risk Statements  20/21/22-22
Safety Statements  36/37-24/25
WGK Germany  3
RTECS  AM6913800
HS Code  29329990

ROTTLERIN price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 557370 Rottlerin - CAS 82-08-6 - Calbiochem 82-08-6 10mg $144 2024-03-01 Buy
Cayman Chemical 12006 Rottlerin ≥90% 82-08-6 10mg $62 2024-03-01 Buy
Cayman Chemical 12006 Rottlerin ≥90% 82-08-6 50mg $239 2024-03-01 Buy
Tocris 1610 Rottlerin ≥95%(HPLC) 82-08-6 50 $402 2021-12-16 Buy
Tocris 1610 Rottlerin ≥95%(HPLC) 82-08-6 10 $95 2021-12-16 Buy
Product number Packaging Price Buy
557370 10mg $144 Buy
12006 10mg $62 Buy
12006 50mg $239 Buy
1610 50 $402 Buy
1610 10 $95 Buy

ROTTLERIN Chemical Properties,Uses,Production

Description

Rottlerin (82-08-6) has been reported to inhibit PKCδ selectively however this result has been called into question.1?Displays neuroprotective effects.2?Induces autophagy.3?Cell permeable.

Chemical Properties

orange to brown powder

Uses

Rottlerin is a human ether-a-go-go-related gene (hERG) potassium channel activator.

Definition

ChEBI: A chromenol that is 2,2-dimethyl-2H-chromene substituted by hydroxy groups at positions 5 and 7, a 3-acetyl-2,4,6-trihydroxy-5-methylbenzyl group at position 6 and a (1E)-3-oxo-1-phenylprop-1-en-3-yl group at position 8. A potassium channel opener, it is isolated from Mallotus philippensis.

General Description

Rottlerin is extracted from Mallotus philippinensis. It is a protein kinase Cδ (PKCδ) inhibitor. Rottlerin acts as an uncoupler of mitochondrial respiration from oxidative phosphorylation. It has antitumor, autophagy, anti-proliferative, anti-metastasis and anti-invasive properties.

Biological Activity

Originally reported to inhibit PKC isoforms, with selectivity for PKC δ (K i values are 30, 42, 40, 3-6, 100, and 100 μ M for α , β , γ , δ , ε , λ respectively). Also reported to inhibit CAM kinase III. However, recently shown to inhibit a wide range of protein kinases, and most potently to inhibit PRAK and MAPKAP-K2 (IC 50 values are 1.9 and 5 μ M respectively). Also shown to act as a direct mitochondrial uncoupler.

Biochem/physiol Actions

Recently, Rottlerin (mallotoxin) has been shown to be a potent activator of the large conductance voltage and Ca2 activated K+ channel and to potently leftward shift the conductance-voltage relationship of the channel. Mallatoxin tested on hERG channels increased both step and tail hERG current by leftward shifting the voltage dependence of hERG activation and slowing channel deactivation. These actions distinguish Mallatoxin as a novel naturally occurring hERG channel activator.

storage

+4°C

References

1) Davies et al. (2000), Specificity and mechanism of action of some commonly used protein kinase inhibitors; Biochem. J., 351 95 2) Zhang et al. (2007), Neuroprotective effect of protein kinase C delta inhibitor rottlerin in cell culture and animal models of Parkinson’s disease; J. Pharmacol. Exp. Ther., 322 913 3) Balgi et al. (2009), Screen for chemical modulators of autophagy reveals novel therapeutic inhibitors of mTORC1 signaling; PLoS One, 4 e7124

ROTTLERIN Preparation Products And Raw materials

Raw materials

Preparation Products

ROTTLERIN Suppliers

Global( 134)Suppliers
Supplier Tel Email Country ProdList Advantage
Antai Fine Chemical Technology Co.,Limited
18503026267 info@antaichem.com CHINA 9641 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Aktin Chemicals, Inc.
028-85159085 info@aktinchem.com CHINA 1025 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58
Shaanxi LonierHerb Bio Technology Co Ltd
+86-86-+86-86-029-87551862 +8617702909819 sales006@ingredients-lonier.com China 2603 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Mainchem Co., Ltd. +86-0592-6210733 sale@mainchem.com China 32360 55
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15421 60
3'-[(8-CINNAMOYL-5,7-DIHYDROXY-2,2-DIMETHYL-2H-1-BENZOPYRAN-6-YL)METHYL]-2',4',6'-TRIHYDROXY-5'-METHYLACETOPHENONE 4’,6’-trihydroxy-5’-methyl-methyl)-2 acetophenone,3’-((8-cinnamoyl-5,7-dihydroxy-2,2-dimethyl-2h-1-benzopyran-6-yl) 2-Propen-1-one, 1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl]-3-phenyl-, (2E)- 1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2h-1-benzopyran-8-yl]-3-phenyl-2-propen-1-one (E)-1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl]-3-phenyl-2-propen-1-one Rottlerin,98% Rottlerin, 98% 10MG ROTTLERIN NSC 56346 NSC 94525 Rottlerin (Mallotoxin MALLOTOXIN kamalin (E)-1-(6-(3-Acetyl-2,4,6-trihydroxy-5-methylbenzyl)-5,7-dihydroxy-2,2-dimethyl-2H-chromen-8-yl)-3-phenylprop-2-en-1-one Rottierin 82-08-6 1982-8-6 C30H28O8 Kinase/Phosphatase Biology Protein Kinase C, Calcium/Calmodulin-dependent protein Kinase (PKC and CaMK) Serine/Threonine Kinase Inhibitors Cell Signaling and Neuroscience Cell Biology BioChemical Aromatic Phenols Protein Kinase