Herbimycin A

Modify Date: 2024-01-04 12:16:11

Herbimycin A Structure
Herbimycin A structure
Common Name Herbimycin A
CAS Number 70563-58-5 Molecular Weight 574.662
Density 1.2±0.1 g/cm3 Boiling Point 752.4±60.0 °C at 760 mmHg
Molecular Formula C30H42N2O9 Melting Point N/A
MSDS Chinese USA Flash Point 408.8±32.9 °C

 Use of Herbimycin A


Herbimycin A, an ansamycin antibiotic, acts as a Src family kinase inhibitor. Herbimycin A binds to the SH domain and inhibits the activity of p60v-src and p210BCR-ABL. Herbimycin A inhibits Hsp90 and impairs recovery from heat shock. Herbimycin A exhibits antiangiogenic activity in endothelial cells in vitro.

 Names

Name herbimycin
Synonym More Synonyms

 Herbimycin A Biological Activity

Description Herbimycin A, an ansamycin antibiotic, acts as a Src family kinase inhibitor. Herbimycin A binds to the SH domain and inhibits the activity of p60v-src and p210BCR-ABL. Herbimycin A inhibits Hsp90 and impairs recovery from heat shock. Herbimycin A exhibits antiangiogenic activity in endothelial cells in vitro.
Related Catalog

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 752.4±60.0 °C at 760 mmHg
Molecular Formula C30H42N2O9
Molecular Weight 574.662
Flash Point 408.8±32.9 °C
Exact Mass 574.289001
PSA 152.48000
LogP 2.12
Vapour Pressure 0.0±2.5 mmHg at 25°C
Index of Refraction 1.545
Storage condition −20°C
Water Solubility DMSO: 7.5 mg/mL DMSO stock solution can be diluted in phosphate buffered saline. The ratio of buffer:DMSO should be greater than 500:1.

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
LX8930000
CHEMICAL NAME :
Geldanamycin, 17-demethoxy-15-methoxy-11-O-methyl-, (15R)-
CAS REGISTRY NUMBER :
70563-58-5
LAST UPDATED :
199209
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C30-H42-N2-O9
MOLECULAR WEIGHT :
574.74

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
19 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JANTAJ Journal of Antibiotics. (Japan Antibiotics Research Assoc., 2-20-8 Kamiosaki, Shinagawa-ku, Tokyo, 141, Japan) V.2-5, 1948-52; V.21- 1968- Volume(issue)/page/year: 33,1114,1980

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases 22-24/25-36-26
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS LX8930000
HS Code 29419000

 Synthetic Route

 Precursor & DownStream

Precursor  1

DownStream  0

 Customs

HS Code 29419000

 Articles31

More Articles
Herbimycins D-F, ansamycin analogues from Streptomyces sp. RM-7-15.

J. Nat. Prod. 76(9) , 1619-26, (2013)

Bacterial strains belonging to the class actinomycetes were isolated from the soil near a thermal vent of the Ruth Mullins coal fire (Appalachian Mountains of eastern Kentucky). High-resolution electr...

Herbimycin A inhibits cell growth with reversal of epithelial-mesenchymal transition in anaplastic thyroid carcinoma cells.

Biochem. Biophys. Res. Commun. 455(3-4) , 363-70, (2014)

We aimed to elucidate the effect of herbimycin A (HMA), a heat shock protein 90 inhibitor, on cell growth and epithelial-mesenchymal transition (EMT) in anaplastic thyroid carcinoma (ATC) cells. HMA i...

Effects of tyrosine kinase and phosphatase inhibitors on microtubules in Arabidopsis root cells.

Cell Biol. Int. 32(6) , 630-7, (2008)

To investigate the role of tyrosine phosphorylation/dephosphorylation processes in plant cells the morphology of Arabidopsis thaliana primary roots and the organization of cortical microtubules (MTs) ...

 Synonyms

2-Azabicyclo[16.3.1]docosa-4,6,10,18,21-pentaene-3,20,22-trione, 9-[(aminocarbonyl)oxy]-8,13,14,17-tetramethoxy-4,10,12,16-tetramethyl-, (4E,6Z,8S,9S,10E,12S,13R,14S,16S,17R)-
herbimycin
MFCD00151702
Herbimycin A
(4E,6Z,8S,9S,10E,12S,13R,14S,16S,17R)-9-[(aminocarbonyl)oxy]-8,13,14,17-tetramethoxy-4,10,12,16-tetramethyl-2-azabicyclo[16.3.1]docosa-4,6,10,18,21-pentaene-3,20,22-trione
(15R)-17-demethoxy-15-methoxy-11-O-methylgeldanamycin
(4E,6Z,8S,9S,10E,12S,13R,14S,16S,17R)-8,13,14,17-Tetramethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl carbamate