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Omtriptolide

Product Name
Omtriptolide
CAS No.
195883-06-8
Chemical Name
Omtriptolide
Synonyms
OMTRIPTOLIDE;Unii-D36elm729p;Butanedioic acid, 3-(3,4-dichlorophenyl)-2-(ethoxymethyl)-8-methyl-, 1-[(3bS,4aS,5aR,6R,6aS,7aS,7bS,8aS,8bS)-1,3,3b,4,4a,6,6a,7a,7b,8b,9,10-dodecahydro-8b-methyl-6a-(1-methylethyl)-1-oxotrisoxireno[4b,5:6,7:8a,9]phenanthro[1,2-c]furan-6-yl] ester
CBNumber
CB31509125
Molecular Formula
C24H28O9
Formula Weight
460.47
MOL File
195883-06-8.mol
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Omtriptolide Property

Melting point:
109-111 ºC
Boiling point:
691.4±55.0 °C(Predicted)
Density 
1.49
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
4.36±0.17(Predicted)
form 
Solid
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-6982
Product name
Omtriptolide
Purity
98.23%
Packaging
1mg
Price
$150
Updated
2021/12/16
ChemScene
Product number
CS-6982
Product name
Omtriptolide
Purity
98.23%
Packaging
5mg
Price
$450
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0009669
Product name
OMTRIPTOLIDE
Purity
95.00%
Packaging
5MG
Price
$504.86
Updated
2021/12/16
ChemScene
Product number
CS-6982
Product name
Omtriptolide
Purity
98.23%
Packaging
10mg
Price
$650
Updated
2021/12/16
ChemScene
Product number
CS-6982
Product name
Omtriptolide
Purity
98.23%
Packaging
25mg
Price
$1300
Updated
2021/12/16
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Omtriptolide Chemical Properties,Usage,Production

Uses

Antineoplastic.

in vivo

In a mouse model of cisplatin-induced AKI, omtriptolide results in a significant decrease in blood urea nitrogen (BUN), serum creatinine, and acute tubular necrosis (ATN) score, and a nonsignificant increase in tubular apoptosis score in AKI. The protection of omtriptolide against AKI is associated with a decrease in p-ERK and is independent of MKP-1 and proinflammatory cytokines[1]. In a mouse heterotopic tracheal allograft model of obliterative airway disease, omtriptolide attenuates airway obliteration and inhibits accumulation of inflammatory cells, and therefore may have preventive or therapeutic benefits for patients with obliterative airway disease following lung transplantation[2]. Omtriptolide inhibits fibrosis in the bleomycin group when given the same day or 5 days after bleomycin. Omtriptolide also markedly reduces the number of myofibroblasts in the bleomycin treatment group[3]. Omtriptolide inhibits in vivo both CD4+Vbeta3+ and CD8+Vbeta3+ T cell (alloreactive T cells in this model) expansion in the spleen by 64.09 and 34.02%, respectively, at the time when Vbeta3+ cell expansion is in the logarithmic phase (day 3 after transplantation)[4].

IC 50

ERK

Omtriptolide Preparation Products And Raw materials

Raw materials

Preparation Products

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Omtriptolide Suppliers

Shanghai Fuhe Chemistry Technology Co., Ltd.
Tel
0086-21-67651709
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0086-21-67651705
Email
cfx759@hotmail.com
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China
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410
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Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
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China
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9803
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58
Fan De(Beijing) Biotechnology Co., Ltd.
Tel
15911056312
Email
liming@bio-fount.com
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China
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9729
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Beijing xinyanhui pharmaceutical research and development co., LTD
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13969155946
Email
1461866103@qq.com
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China
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16111
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
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China
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cjbscvictory
Tel
13348960310
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3003867561@qq.com
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China
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Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 15801484223;
Email
psaitong@jm-bio.com
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China
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TargetMol Chemicals Inc.
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4008200310
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marketing@tsbiochem.com
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China
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Suzhou Meishi Biotechnology Co., Ltd.
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1173954148q
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meishipharma@126.com
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China
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RD International Technology Co., Limited
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18024082417
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market@ubiochem.com
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China
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Yeasen Biotechnology (Shanghai) Co Ltd
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400-6111-883 13121892008
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marketing@yeasen.com
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Biosynth Biological Technology (Suzhou) Co Ltd
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51288865780
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sales@biosynth.com
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Adooq Bioscience LLC
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400-025-6535
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Jinan Dingguo Biotechnology Co., Ltd.
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CHINA
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Guangzhou Haotian Biotechnology Co., Ltd.
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Shanghai Hao Zhun Biological Technology Co., Ltd.
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195883-06-8, OmtriptolideRelated Search:


  • OMTRIPTOLIDE
  • Unii-D36elm729p
  • Butanedioic acid, 3-(3,4-dichlorophenyl)-2-(ethoxymethyl)-8-methyl-, 1-[(3bS,4aS,5aR,6R,6aS,7aS,7bS,8aS,8bS)-1,3,3b,4,4a,6,6a,7a,7b,8b,9,10-dodecahydro-8b-methyl-6a-(1-methylethyl)-1-oxotrisoxireno[4b,5:6,7:8a,9]phenanthro[1,2-c]furan-6-yl] ester
  • 195883-06-8