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Sargramostim   Drugbank  ID : Sargramostim   Drugbank  ID :

Sargramostim Drugbank ID : - PowerPoint Presentation

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Uploaded On 2022-06-15

Sargramostim Drugbank ID : - PPT Presentation

DB00020 Protein chemical formula C 639 H 1006 N 168 O 196 S 8 Protein average weight 144345000 Description Sargramostim is a human recombinant granulocyte macrophage colonystimulating factor GMCSF expressed in yeast It is a glycoprotein that is 127 residues ID: 919321

bone marrow receptor cells marrow bone cells receptor subunit factor csf transplant leukine chemotherapy normal stimulating leucomax alpha granulocyte

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Presentation Transcript

Slide1

Sargramostim

Drugbank

ID :

DB00020

Protein chemical

formula :

C

639

H

1006

N

168

O

196

S

8

Protein

average

weight :

14434.5000

Slide2

Description

:

Sargramostim

is a human recombinant granulocyte macrophage colony-stimulating factor (GM-CSF) expressed in yeast. It is a glycoprotein that is 127 residues. Substitution of Leu23 leads to a difference from native protein.

Indication

:

For the treatment of cancer and bone marrow transplant

Pharmacodynamics

:

Sargramostim

is used in the treatment of bone marrow transplant recipients or those exposed to chemotherapy an recovering from

acut

myelogenous

leukemia

,

Leukine

or GM-CSF is a hematopoietic growth factor which stimulates the survival,

clonal

expansion (proliferation) and differentiation of hematopoietic progenitor cells. GM-CSF is also capable of activating mature granulocytes and macrophages. After a bone marrow transplant or chemotherapy, patients have a reduced capacity to produce red and white blood cells. Supplementing them with external sources of GM-CSF helps bring the level of

neutrophils

back to normal so that they can better fight infections.

Slide3

Mechanism of action

:

Sargramostim

binds to the Granulocyte-macrophage colony stimulating factor receptor (GM-CSF-R-alpha or CSF2R) which stimulates a JAK2 STAT1/STAT3 signal transduction pathway. This leads to the production of

hemopoietic

cells and

neutrophils

Clearance :

420

mL/min/m2 [Normal people with liquid LEUKINE (IV)

]

431

mL/min/m2 [Normal people with lyophilized LEUKINE (IV)

]

549 mL/min/m2 [Normal people with liquid LEUKINE (SC

)

]

529

mL/min/m2 [Normal people with lyophilized LEUKINE (SC)].

Slide4

Targets

:

Granulocyte-macrophage colony-stimulating factor receptor subunit alpha,Interleukin-3 receptor subunit

alpha,Cytokine

receptor common subunit beta,Syndecan-2,Bone marrow

proteoglycan

Affected organisms

:

Humans and other mammals

Slide5

Categories

:

Immunosuppressive Agents

Patents

:

Country Patent Number Approved Expires

Canada 1341150 2000

-12-

05 2017

-12-05

Sequence

:

APARSPSPSTQPWEHVNAIQEALRLLNLSRDTAAEMNETVEVISEMFDLQEPTCLQTRLELYKQGLRGSLTKLKGPLTMMASHYKQHCPPTPETSCATQIITFESFKENLKDFLLVIPFDCWEPVQE

Slide6

Brands

:

Leucomax

Company :

Novartis

Description :

Leucomax

contains a chemical which stimulates the colonies of white stem cells within the bone marrow causing the level of granulocytes in the blood to rise. Increasing the levels granulocytes in the blood stream reduced the risk and severity of infection. In the same way chemotherapy affects the rapidly dividing white cells it can also affect the platelets. The cells which make platelets are also found within the bone marrow, called "platelet stem cells -

megacaryocytes

".

Leucomax

also stimulates

megacaryocytes

and increases the number of platelets into the blood stream thereby reducing the risk of bleeding. (Granulocyte &

Megacaryocyte

stimulating factor - GM-CSF)

Used for/Prescribed for :

Used for: Reducing severe, life-threatening, or fatal infections after chemotherapy for acute

myelogenous

leukemia

(AML). It is also used to help increase the success of

autologous

bone marrow transplant and to help increase survival in patients who have bone marrow transplant failure.

Form :

solution

Route of administration :

subcutaneous and intravenous Injection

Slide7

Dosage :

In case of Intravenous Chemotherapy-induced

neutropenia

in Adult: 250 mcg/m 2 daily for up to 42 days as required, to be given as IV infusion over 4 hr

Side effects :

It is common to have aching bones and joints for 2-3 days starting 1-2 days after the start of the injections. This is usually mild and is caused by the bone marrow working harder to More white cells. Occasionally it is more troublesome and pain killers are required. (Provided you don't have a temperature

paracetamol

is often helpful, it is not strong enough ask your doctor about anti-inflammatory drugs. Remember if you feel unwell check your temperature before you due to take your next tablet).

Slide8

General references

:

Granulocyte-macrophage colony-stimulating factor receptor subunit alpha,Interleukin-3 receptor subunit

alpha,Cytokine

receptor common subunit beta,Syndecan-2,Bone marrow

proteoglycan

.

Slide9

References

:

http://www.cancernet.co.uk/

leucomax.htm

http://www.igenericdrugs.com/?s=leucomax%20%28novartis%29