Temsirolimus (CCI-779, NSC 683864) - ≥98%, high purity , FK506-binding protein 1A inhibitor, CAS No.162635-04-3, FK506-binding protein 1A inhibitor

Item Number
T126606
Grouped product items
SKUSizeAvailabilityPrice Qty
T126606-5mg
5mg
3
$77.90
T126606-25mg
25mg
3
$247.90
T126606-100mg
100mg
2
$641.90

Selective mTORC1 complex inhibitor (IC 50 = 1.76 µM)

Basic Description

SynonymsAB01274736-01 | DTXSID2040945 | CBPNZQVSJQDFBE-FUXHJELOSA-N | NCGC00167518-09 | TEMSIROLIMUS (MART.) | temsirolimusum | BRD-K08177763-001-02-6 | L01XE09 | TEMSIROLIMUS [INN] | TEMSIROLIMUS [VANDF] | MFCD00934421 | Temsirolimus (CCI-779, NSC 683864) | Tox2
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsTemsirolimus (also known as CCI-779) is a recently developed mTOR inhibitor. with improved aqueous solubility and more favorable pharmaceutical properties compared with the parent compound rapamycin.Selective mTORC1 complex inhibitor (IC 50 = 1.76 µM). Wa
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionFK506-binding protein 1A inhibitor
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Temsirolimus (CCI-779) directly inhibits mTOR kinase activity with IC50 values of 1.76 ± 0.15 μM.
A potent inhibitor of FRAP (mTOR) kinase activity


application:

Temsirolimus is used as a rapamycin derivative with anti-cancer activity that inhibits mTOR. Temsirolimus is an antiproliferative and antiangiogenic, the first-in-class mTOR inhibitor approved for the treatment of patients with advanced poor prognosis renal cell carcinoma.

AI Insight

Product Properties

ALogP5.6

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid504764358
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504764358
IUPAC Name [(1R,2R,4S)-4-[(2R)-2-[(1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18-dihydroxy-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-2,3,10,14,20-pentaoxo-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraen-12-yl]propyl]-2-methoxycyclohexyl] 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoate
INCHI InChI=1S/C56H87NO16/c1-33-17-13-12-14-18-34(2)45(68-9)29-41-22-20-39(7)56(67,73-41)51(63)52(64)57-24-16-15-19-42(57)53(65)71-46(30-43(60)35(3)26-38(6)49(62)50(70-11)48(61)37(5)25-33)36(4)27-40-21-23-44(47(28-40)69-10)72-54(66)55(8,31-58)32-59/h12-14,17-18,26,33,35-37,39-42,44-47,49-50,58-59,62,67H,15-16,19-25,27-32H2,1-11H3/b14-12+,17-13+,34-18+,38-26+/t33-,35-,36-,37-,39-,40+,41+,42+,44-,45+,46+,47-,49-,50+,56-/m1/s1
InChi Key CBPNZQVSJQDFBE-FUXHJELOSA-N
Canonical SMILES CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)OC(=O)C(C)(CO)CO)C)C)O)OC)C)C)C)OC
Isomeric SMILES C[C@@H]1CC[C@H]2C[C@@H](/C(=C/C=C/C=C/[C@H](C[C@H](C(=O)[C@@H]([C@@H](/C(=C/[C@H](C(=O)C[C@H](OC(=O)[C@@H]3CCCCN3C(=O)C(=O)[C@@]1(O2)O)[C@H](C)C[C@@H]4CC[C@H]([C@@H](C4)OC)OC(=O)C(C)(CO)CO)C)/C)O)OC)C)C)/C)OC
WGK Germany 3
PubChem CID 6918289
Molecular Weight 1030.29

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDateItem
I2213098Certificate of AnalysisJun 20, 2024 T126606
I2213171Certificate of AnalysisJun 20, 2024 T126606
I2213172Certificate of AnalysisJun 20, 2024 T126606

Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS09
Signal Danger
Hazard Statements

H410:Very toxic to aquatic life with long lasting effects

H360:May damage fertility or the unborn child

Precautionary Statements

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P405:Store locked up.

P501:Dispose of contents/container to ...

P391:Collect spillage.

P203:Obtain, read and follow all safety instructions before use.

P318:if exposed or concerned, get medical advice.

WGK Germany 3

Related Documents

Reviews

Customer Reviews

References

1. Kuroshima K et al..  (2020)  Potential new therapy of Rapalink-1, a new generation mammalian target of rapamycin inhibitor, against sunitinib-resistant renal cell carcinoma..  Cancer Sci,  111  (5): (1607-1618).  [PMID:32232883]
2. Stepanenko AA et al..  (2016)  Temozolomide promotes genomic and phenotypic changes in glioblastoma cells..  Cancer Cell Int,  16  (36).  [PMID:27158244]

Solution Calculators