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Temsirolimus

Temsirolimus Structure
CAS No.
162635-04-3
Chemical Name:
Temsirolimus
Synonyms
40-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate]-rapamycin;C15182;CS-442;CCL-779;NSC 683864;TEMSIROLIMUS;Simultaneous;TeMsiroliMus (~90%);Temsirolimus, >=98%;CCI-779; NSC 683864
CBNumber:
CB3506811
Molecular Formula:
C56H87NO16
Molecular Weight:
1030.29
MOL File:
162635-04-3.mol
MSDS File:
SDS
Modify Date:
2024/4/22 13:28:10

Temsirolimus Properties

Melting point 99-101°C
Boiling point 1048.4±75.0 °C(Predicted)
Density 1.21
Flash point 587.8℃
storage temp. room temp
solubility Soluble in chloroform, methanol.
pka 10.40±0.70(Predicted)
form powder
color white to off-white
Merck 14,9142
InChIKey CBPNZQVSJQDFBE-FUXHJELOSA-N

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Danger
Hazard statements  H360-H413
Precautionary statements  P501-P273-P202-P201-P280-P308+P313-P405
Safety Statements  24/25
WGK Germany  3
RTECS  VE6257000
HS Code  29349990
NFPA 704
0
1 0

Temsirolimus price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) PZ0020 Temsirolimus ≥98% (HPLC) 162635-04-3 5MG ₹14115.8 2022-06-14 Buy
Sigma-Aldrich(India) PZ0020 Temsirolimus ≥98% (HPLC) 162635-04-3 25MG ₹51732.68 2022-06-14 Buy
TCI Chemicals (India) T3574 Temsirolimus 162635-04-3 50MG ₹17600 2022-05-26 Buy
Product number Packaging Price Buy
PZ0020 5MG ₹14115.8 Buy
PZ0020 25MG ₹51732.68 Buy
T3574 50MG ₹17600 Buy

Temsirolimus Chemical Properties,Uses,Production

Description

While renal cell carcinoma (RCC) accounts for only 2 3% of all cancers, the 5-year survival rate for advanced RCC disease is only 5 10%, with approximately 13,000 deaths occurring annually (US statistics only). Immunotherapeutic cytokine options, such as IFN-αand IL-2, have traditionally been frontline treatments, but these agents are not efficacious in all patients and can cause serious side effects. In addition, bevacizumab, a monoclonal antibody against VEGF, has also demonstrated prolongation of PFS. The newest entry for this indication focuses on targets that are downstream from VEGF. Temsirolimus is an inhibitor of the serine/threonine kinase mTOR, which is the mammalian target of rapamycin. mTOR has been implicated in cell replication through control of the cell cycle translation of specific mRNAs. Inhibition of mTOR prevents phosphorylation of the 4E binding protein-1 and the 40S ribosomal protein S6 kinase that are responsible for cell cycle protein translation initiation; cell cycle arrest occurs as the result of termination of cell division from the G1 to the S phase. Disruption of mTOR signaling also has antiangiogenic effects that could be deemed essential in combating RCC, which is driven by unregulated angiogenesis. Temsirolimus is the 2,2-bis(hydroxymethyl)propionate ester of rapamycin (sirolimus), a macrolide fungicide isolated from the bacteria Streptomyces hygroscopicus. Similar to its parent sirolimus, temsirolimus interacts with mTOR through its complex with FK-506 binding protein 12.

Chemical Properties

White Solid

Uses

Temsirolimus, a cell cycle inhibitor developed by Wyeth for the treatment of renal cell carcinoma, was launched in the US in 2007. Temsirolimus works by inhibiting mTOR (mammalian target of rapamycin)-driven cell proliferation. Temsirolimus is also being developed for the treatment of mantle cell lymphoma (PhIII) and also as mono- or combination therapy for the treatment of ovarian and endometrium cancer (PhII). Additionally, temsirolimus is being evaluated for the treatment of several other types of cancer as well as multiple sclerosis and rheumatoid arthritis.

General Description

Temsirolimus is an esterified derivative of rapamycinand in a similar manner binds initially to the proteinFKBP-12(FK506-binding protein).This complexthen acts to inhibit the mammalian target of rapamycin(mTOR), a serine-threonine kinase that plays a crucial rolein cell division. It is somewhat unique in its method of kinaseinhibition, because it actually binds to an allostericmodulator of the kinase rather than just binding to theATP-binding site like most other kinase inhibitors.Temsirolimus is available as a 25-mg/mL injection forIV administration in the treatment of advanced RCC. Theagent is extensively metabolized and undergoes rapid hydrolysisof the ester function to give rapamycin that retainsactivity.Additional metabolism is mediated primarilyby CYP3A4 to give several hydroxylated and demethylatedmetabolites that are inactive. The agent and metabolites areeliminated primarily in the feces with half-lives of 17 and55 hours for temsirolimus and rapamycin, respectively.This agent, like rapamycin, possesses immunosuppressantproperties and there is an increased risk of infection.The most serious side effects are interstitial lung disease,perforation of the bowel, and acute renal failure althoughthese occur only rarely. The most commonly seen side effects are rash, weakness, mucositis, nausea, edema, andanorexia.

Temsirolimus Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 272)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Ralington Pharma +91-7948911722 +91-9687771722 Gujarat, India 1350 58 Inquiry
Fresenius Kabi Oncology Limited +91-1243325000 +91-1244885000 Haryana, India 22 58 Inquiry
Concord Biotech Limited +91-2714398200 +91-2714398200 Gujarat, India 22 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
SUN PHARMACEUTICAL INDUSTRIES LTD (+91 22) 4324 4324 New Delhi, India 175 58 Inquiry
BIOCON LTD +91 80 2808 2808 New Delhi, India 39 58 Inquiry
CONCORD BIOTECH LTD +91 79 68138700 New Delhi, India 18 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
42-[3-hydroxy-2-(hydroxymethyl)-2-methylpropa Temsirolimus(CCI-779) TEMSIROLIMUS CCL-779 Rapamycin 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate TeMsiroliMus (CCI-779, Torisel) rapaMycin 42-ester with 3-hydroxy-2-(hydroxyMethyl)-2-Methylpropionic acid 42-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate]rapamycin C15182 TeMsiroliMus (Torisel) TeMsiroliMus (~90%) TeMsiroliMus (Torisel,CCI-779,NSC-683864) TeMsiroliMus (CCI-779, NSC 683864) Rapamycin 42-[3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate Temsirolimus Temsirolimus Rapamycin 42-[3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate 42-[3-Hydroxy-2-methylpropanoate Temsirolimus, >=98% NSC 683864 (1R,2R,4S)-4-{(2R)-2-[(3S,6R,7E,9R,10R,12R,14S,15E,17E,19E,21S,23S,26R,27R,34aS)-9,27-dihydroxy-10,21-dimethoxy-6,8,12,14,20,26-hexamethyl-1,5,11,28,29-pentaoxo-1,4,5,6,9,10,11,12,13,14,21,22,23,24,25,26,27,28,29,31,32,33,34,34a-tetracosahydro-3H-23,27-epoxypyrido[2,1-c][1,4]oxazacyclohentriacontin-3-yl]propyl}-2-methoxycyclohexyl 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate Temsirolimus (mixture of isomers) Temsirolimus USP/EP/BP TemsirolimusQ: What is Temsirolimus Q: What is the CAS Number of Temsirolimus Q: What is the storage condition of Temsirolimus Q: What are the applications of Temsirolimus 162635-04-3 Temsirolimus temsirolimus 162635-04-3 CCI-779; NSC 683864 CS-442 Simultaneous 40-[3-Hydroxy-2-(hydroxymethyl)-2-methylpropanoate]-rapamycin (1R,2R,4R)-4-((R)-2-((3S,6R,7E,9R,10R,12R,14S,15E,17E,19E,21S,23S,26R,27R,34aS)-9,27-Dihydroxy-10,21-dimethoxy-6,8,12,14,20,26-hexamethyl-1,5,11,28,29-pentaoxo-1,4,5,6,9,10,11,12,13,14,21,22,23,24,25,26,27,28,29,31,32,33,34,34a-tetracosahydro-3H-23,27-epoxypyrido[2,1-c][1]oxa[4]azacyclohentriacontin-3-yl)propyl)-2-methoxycyclohexyl 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate 162635-04-3 475271-62-2 C56H87NO16 Antineoplastic protein kinase inhibitors mTOR inhibitor Anti-cancer&immunity PI3K/Akt/mTOR CCI-779, NSC 683864 Inhibitors Akt mTOR PI3K Intermediates & Fine Chemicals Pharmaceuticals