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ALMOTRIPTAN

Description References
Product Name
ALMOTRIPTAN
CAS No.
181183-52-8
Chemical Name
ALMOTRIPTAN
Synonyms
Axert;Almogran;PNU 180638;PNU-180638;Almotriptan;LAS-31416 Malate;1-[[[3-[2-(dimeth;Amotriptan malate;AlmotriptanMaleate;ALMOTRIPTAN MALATE
CBNumber
CB2417037
Molecular Formula
C21H31N3O7S
Formula Weight
469.55
MOL File
181183-52-8.mol
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ALMOTRIPTAN Property

Melting point:
170-172°C
storage temp. 
2-8°C
solubility 
Basic Alcohol (Very Slightly), DMSO (Slightly), Methanol (Slightly, Heated)
form 
powder
color 
white to beige
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Safety

HS Code 
2935904000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H312Harmful in contact with skin

H332Harmful if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P322Specific measures (see …on this label).

P363Wash contaminated clothing before reuse.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML1210
Product name
Almotriptan malate
Purity
≥98% (HPLC)
Packaging
10MG
Price
$138
Updated
2023/06/20
Sigma-Aldrich
Product number
SML1210
Product name
Almotriptan malate
Purity
≥98% (HPLC)
Packaging
50MG
Price
$547
Updated
2023/06/20
Sigma-Aldrich
Product number
1013512
Product name
Almotriptan malate
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200MG
Price
$400
Updated
2022/05/15
TCI Chemical
Product number
A3111
Product name
Almotriptan Malate
Packaging
25MG
Price
$28
Updated
2024/03/01
TCI Chemical
Product number
A3111
Product name
Almotriptan Malate
Packaging
100MG
Price
$74
Updated
2024/03/01
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ALMOTRIPTAN Chemical Properties,Usage,Production

Description

Almotriptan is a kind of triptan drug which can be used for the treatment of migraine headaches. It is belong to a drug category of selective serotonin receptor agonists. It has a high and specificity affinity for serotonin 5-HT receptors, further leading to vascoconstriction of the brain blood vessel and affecting the redistribution of blood flow. These effects stop pain signals from being sent to the brain, and further suppressing the release of certain natural substances which cause pain, nausea and other migraine symptoms. However, it doesn’t prevent migraine attacks.

References

https://en.wikipedia.org/wiki/Almotriptan
https://www.drugbank.ca/drugs/DB00918

Description

Almotriptan is an agonist of the serotonin (5-HT) receptor subtypes 5-HT1B and 5-HT1D (IC50s = 12 and 13 nM, respectively, in a radioligand binding assay). It is selective for human 5-HT1B and 5-HT1D receptors over rat 5-HT1A and human 5-HT2A and 5-HT4 receptors (IC50s = 0.85, 25.1, and 140 μM, respectively). Almotriptan induces contractions in isolated canine saphenous veins (EC50 = 394 nM) but not isolated rabbit renal or mesenteric arteries. It increases carotid vascular resistance in anesthetized cats (ED100 = 11 μg/kg, i.v.) without increasing blood pressure or heart rate. Formulations containing almotriptan have been used in the treatment of migraine headaches.

Chemical Properties

Pale Yellow Solid

Originator

Almogran ,Lundbeck

Uses

Almotriptan is a serotonin 5HT-1B/1D-receptor agonist; antimigraine.

Uses

Almotriptan is a serotonin 5HT1B /1D-receptor agonist used for treatment of migraine.

Uses

anti-migraine agent

Definition

ChEBI: The malate salt of almotriptan.

Manufacturing Process

To a solution of previously dried 1-[[2-carboxy-3-(2-dimethylaminoethyl)-5- indolyl]methanesulphonyl]-pyrrolidine (1.6 g; 0.0442 moles) in anhydrous quinoline (75 ml) and under atmosphere of nitrogen, cuprous oxide (160 mg; 0.0011 moles) was added. The reaction mixture was heated to 190°C for 15 minutes, stirred to room temperature, poured into a mixture of 1 N hydrochloric acid (150 ml) and ethyl acetate (50 ml), shaken and decanted. The aqueous solution was washed several times with ethyl acetate, then solid sodium bicarbonate was added until pH = 7.8, and washed with n-hexane to eliminate the quinoline. The aqueous solution was made alkaline with solid potassium carbonate and extracted with ethyl acetate. The organic solution was dried (Na2SO4), the solvent removed under reduced pressure when a dark oil was obtained (1.3 g; yield 92%). This product was purified by column chromatography with silica gel and methylene chloride:ethanol:ammonium hydroxide (60:8:1) as eluent and a white foam (0.8 g) of 1-[[3-(2- dimethylaminoethyl)-5-indolyl]methanesulphonyl]-pyrrolidine was obtained. To a solution of the above product (0.8 g) in acetone (30 ml), a few drops of hydrogen chloride saturated dioxan solution, were added. The precipitated solid was collected by filtration, washed with acetone and dried to give 1-[(3- (2-(dimethylamino)ethyl)-5-indolyl)methanesulphonyl]-pyrrolidine hydrochloride (0.75 g). Melting point 218°-220°C.
In practice it is usually used as malate salt.

brand name

Axert (Ortho-McNeil).

Therapeutic Function

Migraine therapy

General Description

Almotriptan, marketed in 2000, has the highest oralbioavailability among all triptans. It is metabolizedby both MAO-A and CYP3A4, thus has a more favorableside effects profile when compared with sumatriptan.However, it is only available in a 12.5 mg tablet form.

Biochem/physiol Actions

Almotriptan is a serotonin 5HT-1B/1D-receptor agonist used to treat migraine. Almotriptan has low nanomolar affinity for the 5-HT(1B) and 5-HT(1D) receptors while affinity for 5-HT receptors other than 5-HT(1B/1D) is substantially lower. Affinity for 5-HT(7) and 5-HT(1A) receptors was approximately 40 and 60 times lower than that for 5-HT(1B/1D) receptors, respectively.

ALMOTRIPTAN Preparation Products And Raw materials

Raw materials

Preparation Products

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ALMOTRIPTAN Suppliers

Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
Email
sales@boylechem.com
Country
China
ProdList
2923
Advantage
55
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94838
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76
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6011
Advantage
61
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10194
Advantage
62
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
zhangsn@titansci.com
Country
China
ProdList
14113
Advantage
59
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2127
Advantage
70
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
Country
China
ProdList
17988
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
XiaoGan ShenYuan ChemPharm co,ltd
Tel
0712-0712-2580635 15527768850
Email
1791901229@qq.com
Country
China
ProdList
8849
Advantage
52
Beijing FaMu RuiSi Pharmaceuticals Co.,Ltd
Tel
18901358086
Fax
86-010-61252196
Email
pharma_reese@126.com
Country
China
ProdList
60
Advantage
57
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View Lastest Price from ALMOTRIPTAN manufacturers

Zibo Hangyu Biotechnology Development Co., Ltd
Product
ALMOTRIPTAN 181183-52-8
Price
US $70.00-700.00/kg
Min. Order
10kg
Purity
0.99
Supply Ability
20tons
Release date
2023-10-31
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Almotriptan Malate 181183-52-8
Price
US $0.00/Kg/Bag
Min. Order
100g
Purity
98%min
Supply Ability
10kg
Release date
2021-10-20
Hebei Mingeng Biotechnology Co., Ltd
Product
Almotriptan 181183-52-8
Price
US $200.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000kg/Month
Release date
2022-11-21

181183-52-8, ALMOTRIPTANRelated Search:


  • BUTANEDIOIC ACID, HYDROXY-, COMPD WITH 1-[[[3-[2-(DIMETHYLAMINO)ETHYL]-1H-INDOL-5-YL]METHYL]SULFONYL]PYRROLIDINE
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  • C21H31N3O7S
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