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Ergotamine, with the chemical formula C38H45N5O11, is a complex molecule that belongs to the ergot alkaloid family. These alkaloids are naturally occurring compounds derived from the fungus Claviceps purpurea. Ergotamine is known for its therapeutic effects in treating migraines and cluster headaches, as well as its vasoconstrictive and oxytocic properties, which aid in managing postpartum hemorrhage.

1160844-44-9

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1160844-44-9 Usage

Uses

Used in Pharmaceutical Industry:
Ergotamine is used as a therapeutic agent for the treatment of migraines and cluster headaches. It functions by constricting blood vessels in the brain, thereby alleviating the symptoms associated with these conditions.
Used in Obstetrics and Gynecology:
In the field of obstetrics and gynecology, ergotamine is utilized for its vasoconstrictive and oxytocic effects, making it beneficial in the management of postpartum hemorrhage.

Check Digit Verification of cas no

The CAS Registry Mumber 1160844-44-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,8,4 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1160844-44:
(9*1)+(8*1)+(7*6)+(6*0)+(5*8)+(4*4)+(3*4)+(2*4)+(1*4)=139
139 % 10 = 9
So 1160844-44-9 is a valid CAS Registry Number.

1160844-44-9Relevant academic research and scientific papers

Integrin-targeted nano-sized polymeric systems for paclitaxel conjugation: a comparative study

Eldar-Boock, Anat,Blau, Rachel,Ryppa, Claudia,Baabur-Cohen, Hemda,Many, Ariel,Vicent, María Jesús,Kratz, Felix,Sanchis, Joaquin,Satchi-Fainaro, Ronit

, p. 829 - 844 (2017/10/06)

The generation of rationally designed polymer therapeutics via the conjugation of low molecular weight anti-cancer drugs to water-soluble polymeric nanocarriers aims to improve the therapeutic index. Here, we focus on applying polymer therapeutics to targ

POLYMERIC SYSTEMS AND USES THEREOF IN THERANOSTIC APPLICATIONS

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, (2015/10/05)

Polymeric systems useful for theranostic applications are disclosed. The polymeric systems comprise a fluorescent or fluorogenic moiety and a therapeutically active agent, each attached to the same or different polymeric moiety. The polymeric systems are designed such that a fluorescent signal is generated in response to a chemical event, preferably upon contacting an analyte (e.g., an enzyme) that is over- expressed in a diseased tissue or organ. Probes useful for inclusion in such polymeric systems, processes of preparing such probes and the polymeric systems, and uses thereof in diagnostic and/or theranostic applications are also disclosed.

CONJUGATES OF A POLYMER, A BISPHOSPHONATE AND AN ANTI-ANGIOGENESIS AGENT AND USES THEREOF IN THE TREATMENT AND MONITORING OF BONE RELATED DISEASES

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, (2016/01/26)

Conjugates of polymers or copolymers having attached thereto an anti-angiogenesis agent and a bisphosphonate bone targeting agent, and processes of preparing same, are disclosed. Pharmaceutical compositions containing these conjugates and uses thereof in

Conjugates of a novel 7-substituted camptothecin with RGD-peptides as αvβ3 integrin ligands: An approach to tumor-targeted therapy

Dal Pozzo, Alma,Esposito, Emiliano,Ni, Minghong,Muzi, Laura,Pisano, Claudio,Bucci, Federica,Vesci, Loredana,Castorina, Massimo,Penco, Sergio

, p. 1956 - 1967 (2011/08/21)

Eight conjugates of a novel camptothecin derivative (Namitecan, NMT) with RGD peptides have been synthesized and biologically evaluated. This study focused on factors that optimize the drug linkage to the transport vector. The different linkages investigated consist of heterofunctional glycol fragments and a lysosomally cleavable peptide. The linkage length and conformation were systematically modified with the purpose to understand their effect on receptor affinity, systemic stability, cytotoxicity, and solubility of the corresponding conjugates. Among the new conjugates prepared, C6 and C7 showed high receptor affinity and tumor cell adhesion, acceptable stability in murine blood, and high cytotoxic activity (IC50 = 8 nM). The rationale, synthetic strategy, and preliminary biological results will be presented.

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