Home Categories Almotriptan
LN7136752

Almotriptan , 98% , 154323-57-6

CAS NO.:154323-57-6

Empirical Formula: C17H25N3O2S

Molecular Weight: 335.46

MDL number: MFCD08063597

EINECS: 1312995-182-4

Pack Size Price Stock Quantity
5mg RMB279.20 In Stock
10mg RMB398.40 In Stock
25mg RMB941.60 In Stock
50mg RMB1503.20 In Stock
100mg RMB2309.60 In Stock
others     Enquire
Update time: 2022-07-08

PRODUCT Properties

Boiling point: 538.7±60.0 °C(Predicted)
Density  1.27±0.1 g/cm3(Predicted)
pka 16.92±0.30(Predicted)
form  Solid
color  White to off-white

Description and Uses

Almotriptan was first marketed in Spain as a new medicine against acute attacks of migraine. It is the fifth agent belonging to the “triptan” class to be launched after sumatriptan, naratriptan, zolmitriptan and rizatriptan. This close structural analog of sumatriptan can be prepared in six steps from 4-nitrobenzylsulfonyl chloride with a Fischer indole synthesis as the key step. Almotriptan acts as a dual 5-HT1D/1B agonist with a 35 to 51-fold selectivity versus 5-HT1A and 5-HT7 receptors respectively as well as having insignificant affinity for the most relevant nonserotonergic receptors (K1>1μM). Its agonistic effect on 5-HT,n receptors of trigeminal sensory neurons turns off neurogenic inflammation by inhibiting the release of neuropeptides such as calcitonin gene-related peptide, neurokinin A and substance P. Concomitantly, its action on the 5-HT1B receptors in meningeal arteries relieves the vasodilatation of these vessels associated with migraine attacks. Almotriptan causes selective concentration-dependent vasoconstriction of human meningeal and temporal arteries (with EC50 of 0.03 and 0.7 μM) compared to basilar (EC50 = 3.5 μM) and pulmonary arteries (EC50>10μM) or rabbit mesenteric and renal arteries (EC50>100 μM). Although it is predominantly cleared by the kidneys as unchanged drug (45%) or transformed into inactive metabolites by monoamine oxidase A (MAO-A) and CYP3A4 enzymes in the liver, almotriptan has the highest oral bioavailability (70%) of the triptans and has a half-life of 3.5 h. The therapeutic dose of 12.5 mg is well tolerated, shows a rapid onset of action (30 min) and low recurrence rate compared to sumatriptan.

Serotonin 5HT1B /1D-receptor agonist

Safety

RELATED PRODUCTS