Ansamitocin P-3 structure
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Common Name | Ansamitocin P-3 | ||
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CAS Number | 66584-72-3 | Molecular Weight | 635.145 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 833.1±65.0 °C at 760 mmHg | |
Molecular Formula | C32H43ClN2O9 | Melting Point | 190-192℃ | |
MSDS | Chinese USA | Flash Point | 457.7±34.3 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of Ansamitocin P-3Ansamitocin P-3 is a microtubule inhibitor. Ansamitocin P-3 is a macrocyclic antitumor antibiotic. |
Name | ansamitocin P3 |
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Synonym | More Synonyms |
Description | Ansamitocin P-3 is a microtubule inhibitor. Ansamitocin P-3 is a macrocyclic antitumor antibiotic. |
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Related Catalog | |
Target |
Microtubule[1] |
In Vitro | Ansamitocin P3 potently inhibits the proliferation of MCF-7, HeLa, EMT-6/AR1 and MDA-MB-231 cells in culture with a half-maximal inhibitory concentration of 20±3, 50±0.5, 140±17, and 150±1.1 pM, respectively. Further, Ansamitocin P3 is found to bind to purified tubulin in vitro with a dissociation constant (Kd) of 1.3±0.7 µM. The binding of Ansamitocin P3 induces conformational changes in tubulin. Ansamitocin P3 inhibits the proliferation of MCF-7, HeLa, EMT-6/AR1 and MDA-MB-231 cells in culture in a concentration dependent manner. Flow cytometric analysis of PI-stained cells suggests that Ansamitocin P3 inhibits the cell cycle progression of MCF-7 cells in G2/M phase. For example, 26, 50 and 70% of the cells are found to be in G2/M phase in the absence and presence of 50 and 100 pM Ansamitocin P3, respectively[2]. |
Cell Assay | MCF-7, EMT-6/AR1, HeLa and MDA-MB-231 cells are seeded in 96 well plates. Subsequently, cells are incubated with vehicle (0.1% DMSO) or different concentrations (1-1000 pM) of Ansamitocin P3 for 48 h in MCF-7 cells and 24 h for EMT-6/AR1, HeLa and MDA-MB-231 cells, respectively. The half maximal inhibitory concentration of cell proliferation (IC50) for Ansamitocin P3 is determined by sulforhodamine B assay. Four independent experiments are carried out in MCF-7 cells and three independent sets of experiments are performed in EMT-6/AR1, HeLa and MDA-MB-231 cells[2]. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 833.1±65.0 °C at 760 mmHg |
Melting Point | 190-192℃ |
Molecular Formula | C32H43ClN2O9 |
Molecular Weight | 635.145 |
Flash Point | 457.7±34.3 °C |
Exact Mass | 634.265686 |
PSA | 136.16000 |
LogP | 5.09 |
Vapour Pressure | 0.0±3.2 mmHg at 25°C |
Index of Refraction | 1.583 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H332-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn |
Risk Phrases | 20/22-36/37/38 |
Safety Phrases | 26-36 |
RIDADR | NONH for all modes of transport |
RTECS | OQ2293000 |
~% Ansamitocin P-3 CAS#:66584-72-3 |
Literature: Akimoto; Kawai; Hashimoto; Nomura Chemical and Pharmaceutical Bulletin, 1984 , vol. 32, # 7 p. 2565 - 2570 |
~% Ansamitocin P-3 CAS#:66584-72-3 |
Literature: Chemical and Pharmaceutical Bulletin, , vol. 32, # 7 p. 2565 - 2570 |
~% Ansamitocin P-3 CAS#:66584-72-3 |
Literature: Chemical and Pharmaceutical Bulletin, , vol. 32, # 7 p. 2565 - 2570 |
~% Ansamitocin P-3 CAS#:66584-72-3 |
Literature: Chemical and Pharmaceutical Bulletin, , vol. 32, # 7 p. 2565 - 2570 |
Enhanced production of ansamitocin P-3 by addition of isobutanol in fermentation of Actinosynnema pretiosum.
Bioresour. Technol. 102 , 1863-1868, (2011) Supply of isobutanol to enhance the production of anti-tumor agent ansamitocin P-3 (AP-3) in medium containing agro-industrial residues was investigated with analysis of gene transcription, enzyme act... |
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Amide N-glycosylation by Asm25, an N-glycosyltransferase of ansamitocins.
Chem. Biol. 15(8) , 863-74, (2008) Ansamitocins are potent antitumor maytansinoids produced by Actinosynnema pretiosum. Their biosynthesis involves the initial assembly of a macrolactam polyketide, followed by a series of postpolyketid... |
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Determination of the cryptic stereochemistry of the first PKS chain-extension step in ansamitocin biosynthesis by Actinosynnema pretiosum.
ChemBioChem. 7(8) , 1221-5, (2006) The biosynthesis of the antitumor antibiotic, ansamitocin, involves the assembly of a linear octaketide on the ansamitocin (asm) polyketide synthase (PKS), which is then cyclized to proansamitocin and... |
Ansamitosin P 3 |
Propanoic acid, 2-methyl-, (1S,2R,3S,5S,6S,16E,18E,20R,21S)-11-chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1.0]hexacosa-10,12,1
 4(26),16,18-pentaen-6-yl ester |
ANSAMITOCIN P-3 |
Tam-330 |
(1S,2R,3S,5S,6S,16E,18E,20R,21S)-11-Chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1.0]hexacosa-10(26),11,13,16,18-pentaen-6-yl 2- methylpropanoate |
2'-De(acetylmethylamino)-2'-methylmaytansine |
Propanoic acid, 2-methyl-, (1S,2R,3R,5S,6S,16E,18E,20R,21S)-11-chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1.0]hexacosa-10,12,1
 4(26),16,18-pentaen-6-yl ester |
Anasamitocin P-3 |
(1S,2R,3R,5S,6S,16E,18E,20R,21S)-11-Chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1.0]hexacosa-10(26),11,13,16,18-pentaen-6-yl 2- methylpropanoate |
Maytansinol isobutyrate |
O3-isobutyryl-maytansinol |
(3E,5E,7R,84S)-14-chloro-10t,11c-epoxy-84-hydroxy-12c-isobutyryl-15,7r-dimethoxy-3,9c,11t,15-tetramethyl-(84r'H,86c'H)-15-aza-1(1,3)-benzena-8(4,6)-[1,3]oxazinana-cyclopentadecaphane-3,5-diene-82,14-dione |