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IXABEPILONE

Product Name
IXABEPILONE
CAS No.
219989-84-1
Chemical Name
IXABEPILONE
Synonyms
Ixempra;CS-1169;BMS 247550;Ixempra kit;IXABEPILONE;Bms 247550-1;Unii-K27005np0a;Azi-epothilone B;Aza-epothilone B;IXABEPILONE USP/EP/BP
CBNumber
CB61011739
Molecular Formula
C27H42N2O5S
Formula Weight
506.7
MOL File
219989-84-1.mol
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IXABEPILONE Property

Melting point:
>160°C (dec.)
alpha 
D22 -40.7° (c = 1.0 in chloroform)
Boiling point:
697.8±55.0 °C(Predicted)
Density 
1.122±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
13.73±0.70(Predicted)
form 
White solid.
color 
White to Off-White
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Safety

HS Code 
2941906000
Hazardous Substances Data
219989-84-1(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
23732
Product name
Ixabepilone
Purity
≥98%
Packaging
1mg
Price
$96
Updated
2024/03/01
Cayman Chemical
Product number
23732
Product name
Ixabepilone
Purity
≥98%
Packaging
5mg
Price
$286
Updated
2024/03/01
Cayman Chemical
Product number
23732
Product name
Ixabepilone
Purity
≥98%
Packaging
10mg
Price
$522
Updated
2024/03/01
TRC
Product number
I941990
Product name
Ixabepilone
Packaging
2.5mg
Price
$150
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD45423
Product name
Ixabepilone
Packaging
5mg
Price
$200
Updated
2021/12/16
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IXABEPILONE Chemical Properties,Usage,Production

Description

Ixabepilone, a semisynthetic analog of epothilone B, was launched for the treatment of metastatic or locally advanced breast cancer. It is indicated for use in combination with capecitabine in patients who have previously failed treatment with an anthracycline such as doxorubicin and a taxane such as paclitaxel. It is also approved as monotherapy for the treatment of metastatic or locally advanced breast cancer in patients whose tumors are resistant or refractory to anthracyclines, taxanes, and capecitabine. Ixabepilone is the first member of the epothilone family of anticancer agents to be approved. Epothilones are novel cytotoxic macrolides derived from bacterial fermentation.
Like the taxanes, their mechanism of action involves binding to and stabilizing microtubules, which results in mitotic arrest and apoptosis.
The most common adverse reactions (X20%) associated with ixabelipone as monotherapy or in combination with capecitabine were peripheral sensory neuropathy, fatigue/asthenia, myalgia/arthralgia, alopecia, nausea, vomiting, stomatitis/ mucositis, diarrhea, and musculoskeletal pain. The most common hematologic abnormalities (W 40%) include neutropenia, leukopenia, anemia, and thrombocytopenia. Ixabelipone in combination with capecitabine is contraindicated in patients with AST or ALT W2.5 ULN (upper limit of normal) or bilirubin W1 ULN due to increased risk of toxicity and neutropenia-related death.

Description

Ixabepilone is an epothilone with broad-spectrum anticancer activity against a panel of 21 cancer cell lines (IC50s = 1.4-34.5 nM). It stabilizes and induces the polymerization of microtubules and induces cell cycle arrest during mitosis. Ixabepilone is cytotoxic to HCT116/VM46 and A2780Tax clonogenic cells, which are resistant to paclitaxel (; IC90s = 16 and 12.3 nM, respectively, for colony growth inhibition). In vivo, ixabepilone (6.3 and 10 mg/kg, i.v., respectively) shows antitumor activity in paclitaxel-resistant human Pat-21 breast carcinoma and HCT116/VM46 colon carcinoma mouse xenograft models with log cell kill (LCK) values of 1.6 and 2.4, respectively. Ixabepilone (10 mg/kg, i.v.) also increases the time for tumors to quadruple in volume by 7.2, 9, 6.5, 4.7, and >10 weeks, respectively, in mice implanted with Rh18 rhabdomyosarcoma, NB1643 neuroblastoma, WT5 Wilms'' tumor, OS29 osteosarcoma, and BT29 brain carcinoma cells. Formulations containing ixabepilone have used in the treatment of metastatic breast cancer.

Originator

BMS (US)

Uses

Ixabepilone is an anti-tumor agent used in the treatment of patients suffering from solid tumors, such as metastatic breast cancer.

Uses

Antineoplastic; antimitotic.

Definition

ChEBI: A macrocycle that is a lactam analogue of epothilone B. Binds directly to beta-tubulin subunits on microtubules, leading to suppression of microtubule dynamics.

brand name

Ixempra

General Description

The epothilones are macrocyclic lactones that have a mechanismof action similar to that of the taxanes but offer severaladvantages.Ixabepilone is the semisyntheticamide analog of epothilone B that is isolated from themyxobacterium Sorangium cellulosum. The epothilonesshowed potent in vitro activity but greatly decreased activityin vivo caused by metabolic instability via hydrolysis ofthe macrocyclic lactone. Conversion to the lactam increasedstability and maintained in vivo activity. Ixabepilone hasbeen recently (2007) approved for the treatment of metastaticbreast cancer that is resistant to the taxanes. The agent isbelieved to bind to the same site occupied by the taxanes.Molecular modeling studies have been utilized to identifya common pharmacophore between the taxanes andepothilones.Like the taxanes, ixabepilone binds to β-tubulin and stabilizesmicrotubules resulting in cell death.The agent is usefulin cancers that have become resistant to the taxanes, becauseit is not removed by Pgp and is still capable of binding to altered beta tubulin to which the taxanes no longer bind.Increased water solubility also allows the agent to be administeredwithout the need for Cremophor EL, reducing thechance of hypersensitivity reactions. The current indicationsfor the agent are in metastatic breast cancer in combinationwith capecitabine after the failure of an anthracycline and ataxane and as monotherapy in metastatic breast cancer afterfailure of an anthracycline, a taxane, and capecitabine. Theagent is extensively metabolized in the liver primarily byCYP3A4 to give over 30 different metabolites. Eliminationoccurs primarily in the feces (65%) with a smaller amount(21%) occurring in the urine. The terminal elimination halflifeis 52 hours. Major toxicities associated with the useof ixabepilone have included peripheral neuropathy andmyelosuppression occurring as neutropenia. Occurring lessfrequently are alopecia, nausea, vomiting, mucositis, diarrhea,and muscle pain.

Synthesis

The synthesis is described in the scheme, and was initiated by treating epothilone B (56) with sodium azide, tetrabutylammonium chloride, ammonium chloride, trimethylphosphine and tris-(dibenzylideneacetone)-dipalladium(0) chloroform which gave the ring-opened amino acid 57 in 96% yield. It has been proposed that this reaction proceeds via initial ring-opening -allyl palladium complex formation followed by trapping with azide and subsequent reduction to the desired amine. Lactamization of the acyclic amino carboxylic acid 57 by reaction with K2CO3, HOBt and EDCI provided ixabepilone (VIII) in 93% yield. Re-crystallization from cyclohexane/ethyl acetate afforded ixabepilone in 56% overall yield from epothilone B.

in vitro

in a large panel of tumor cell lines, bms-247550 was as active as epothilone b in inducing cytotoxicity. of the 21 cells lines tested, the ic50 values were in the range of 1.4–34.5 nm. bms-247550 almost completely blocked cells in mitosis as early as 8 h after the initiation of drug exposureat a concentration close to the ic90 (7.5 nm, clonogenic cytotoxicity assay) [2].

in vivo

bms-247550 has clearly demonstrated antitumor activity that is superior to paclitaxel in both paclitaxel-sensitive and -resistant tumors. bms-247550 was more efficacious than paclitaxel in all five paclitaxel-resistant tumors such as the clinically derived paclitaxel resistant pat-7 ovarian carcinoma, the a2780tax ovarian carcinoma that is resistant to paclitaxel because of tubulin mutations, the hct116/vm46 mdr colon carcinoma, the clinically derived paclitaxel-resistant pat-21 breast carcinoma, and the murine fibrosarcoma m5076. bms-247550 produced antitumor activity equivalent to paclitaxel against three paclitaxel-sensitive human tumor xenografts such as a2780 human ovarian carcinoma, hct116, and ls174t human colon carcinoma [2].

References

[1]. lee fy1, borzilleri r,fairchild cr, kim sh, long bh, reventos-suarez c, vite gd, rose wc, kramer ra.bms-247550: a novel epothilone analog with a mode of action similar to paclitaxel but possessing superior antitumor efficacy. clin cancer res.2001 may;7(5):1429-37
[2]. denduluri n, low j a, lee j j, et al. phase ii trial of ixabepilone, an epothilone b analog, in patients with metastatic breast cancer previously untreated with taxanes[j]. journal of clinical oncology, 2007, 25(23): 3421-3427.
[3]. shannon puhalla, adam brufsky. ixabepilone: a new chemotherapeutic option for refractory metastatic breast cancer. biologics. 2008 sep; 2(3): 505–515.

IXABEPILONE Preparation Products And Raw materials

Raw materials

Preparation Products

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IXABEPILONE Suppliers

Shandong Jirun Biomedical Technology Co., Ltd.
Tel
0539-0539-8613587 17661611089
Fax
qq2639273505
Email
2639273505@qq.com
Country
China
ProdList
171
Advantage
58
Shandong Chenxi Pharmaceutical Co., Ltd.
Tel
+86-0531-88803416 13153166250
Fax
0531-88803416
Email
sales@chemedpharma.com
Country
China
ProdList
208
Advantage
58
Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2922
Advantage
55
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6005
Advantage
61
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14103
Advantage
59
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Chemsky (shanghai) International Co.,Ltd
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
15402
Advantage
60
Wuhan Sunrise Technology Development Co., Ltd.
Tel
27-027-83314682 13554138826
Fax
+86 (27) 8331-4682
Email
whsrtech@vip.163.com
Country
China
ProdList
230
Advantage
62
Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
sales@meilune.com
Country
China
ProdList
4727
Advantage
58
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
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View Lastest Price from IXABEPILONE manufacturers

shandong perfect biotechnology co.ltd
Product
Ixabepilone 219989-84-1
Price
US $0.00/KG
Min. Order
1KG
Purity
98% HPLC
Supply Ability
5000kgs
Release date
2023-07-07
Shaanxi Haibo Biotechnology Co., Ltd
Product
Ixabepilone 219989-84-1
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000ton
Release date
2023-09-07
WUHAN CIRCLE POWDER TECHNOLOGY CO.,LTD
Product
IXABEPILONE 219989-84-1
Price
US $0.00/KG
Min. Order
100g
Purity
98%+
Supply Ability
100kg
Release date
2021-05-07

219989-84-1, IXABEPILONERelated Search:


  • IXABEPILONE
  • (1R,5S,6S,7R,10S,14S,16S)-6,10-dihydroxy-1,5,7,9,9-pentamethyl-14-[(E) -1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-17-oxa-13-azabicyclo[14. 1.0]heptadecane-8,12-dione
  • Aza-epothilone B
  • Bms 247550-1
  • Ixempra
  • Ixempra kit
  • Unii-K27005np0a
  • Azi-epothilone B
  • BMS 247550
  • Ixabepilone BMS-247550
  • Ixabepilone, Free Base, >99%
  • Ixabepilone (Azaepothilone B
  • 17-Oxa-4-azabicyclo[14.1.0]heptadecane-5,9-dione,7,11-dihydroxy-8,8,10,12,16-pentaMethyl-3-[(1E)-1-Methyl-2-(2-Methyl-4-thiazolyl)ethenyl]-,(1S,3S,7S,10R,11S,12S,16R)-
  • Ixabepilone (1R,5S,6S,7R,10S,14S,16S)-6,10-Dihydroxy-1,5,7,9,9-pentamethyl-14-[(E)-1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-17-oxa-13-azabicyclo[14.1.0]heptadecane-8,12-dione
  • (1S,3S,7S,10R,11S,12S,16R)-7,11-dihydroxy-8,8,10,12,16-pentamethyl-3-[(1E)-1-methyl-2-(2-methyl-4-thiazolyl)ethenyl]-17-Oxa-4-azabicyclo[14.1.0]heptadecane-5,9-dione
  • CS-1169
  • ixabepilone 219989-84-1
  • IXABEPILONE USP/EP/BP
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  • (1S,3S,7S,10R,11S,12S,16R)-7,11-Dihydroxy-8,8,10,12,16-pentamethyl-3-((E)-1-(2-methylthiazol-4-yl)prop-1-en-2-yl)-17-oxa-4-azabicyclo[14.1.0]heptadecane-5,9-dione
  • 219989-84-1
  • C27H42N2O5S
  • API