Ikarugamycin

Modify Date: 2024-01-04 19:05:53

Ikarugamycin Structure
Ikarugamycin structure
Common Name Ikarugamycin
CAS Number 36531-78-9 Molecular Weight 478.62
Density 1.2±0.1 g/cm3 Boiling Point 741.9±60.0 °C at 760 mmHg
Molecular Formula C29H38N2O4 Melting Point N/A
MSDS Chinese USA Flash Point 402.5±32.9 °C
Symbol GHS06
GHS06
Signal Word Danger

 Use of Ikarugamycin


Ikarugamycin is an antibiotic and a inhibitor of clathrin-mediated endocytosis (CME)[1].

 Names

Name ikarugamycin
Synonym More Synonyms

 Ikarugamycin Biological Activity

Description Ikarugamycin is an antibiotic and a inhibitor of clathrin-mediated endocytosis (CME)[1].
Related Catalog
Target

Clathrin-mediated endocytosis[1]

In Vitro Ikarugamycin has an IC50 of 2.7 μM in H1299 cells[1].
References

[1]. Elkin SR, et al. Ikarugamycin: A Natural Product Inhibitor of Clathrin-Mediated Endocytosis. Traffic. 2016 Oct;17(10):1139-49.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 741.9±60.0 °C at 760 mmHg
Molecular Formula C29H38N2O4
Molecular Weight 478.62
Flash Point 402.5±32.9 °C
Exact Mass 478.283173
PSA 95.50000
LogP 5.05
Vapour Pressure 0.0±5.6 mmHg at 25°C
Index of Refraction 1.604
Storage condition -20°C

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NI0625500
CHEMICAL NAME :
Ikarugamycin
CAS REGISTRY NUMBER :
36531-78-9
LAST UPDATED :
199206
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C29-H38-N2-O4
MOLECULAR WEIGHT :
478.69
WISWESSER LINE NOTATION :
T I5 H6 F5-17-5 A CV UVM D&MV DU NU SU C&HTTTT&J AQ L2

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>500 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: 25,271,1972
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
6 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: 25,271,1972
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>250 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: 25,271,1972
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2 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: 25,271,1972

 Safety Information

Symbol GHS06
GHS06
Signal Word Danger
Hazard Statements H301
Precautionary Statements P301 + P310
Hazard Codes T
RIDADR UN 2811 6.1 / PGIII

 Synthetic Route

 Precursor & DownStream

Precursor  2

DownStream  0

 Articles7

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 Synonyms

14,17-Metheno-17H-as-indaceno[3,2-k][1,6]diazacycloheptadecine-9,16,18(1H)-trione, 3-ethyl-2,3,3a,5a,5b,6,10,11,12,13,14,15,20a,21,21a,21b-hexadecahydro-22-hydroxy-2-methyl-, (2R,3R,3aS,5aR,5bS,7Z,14S,19E,20aS,21aR,21bR)-
(3E,5S,7R,8R,10R,11R,12S,15R,16S,18Z,25S)-11-Ethyl-28-hydroxy-10-methyl-21,26-diazapentacyclo[23.2.1.0.0.0]octacosa-1(28),3,13,18-tetraene-2,20,27-trione
Ikarugamycin
tu-6239 c3