Chemical Formula: C30H38O5
Chemical Formula C30H38O5
Found 64 metabolite its formula value is C30H38O5
Iloprost
Iloprost is only found in individuals that have used or taken this drug. It is a synthetic analogue of prostacyclin PGI2. Iloprost dilates systemic and pulmonary arterial vascular beds. It is used to treat pulmonary arterial hypertension (PAH).Iloprost is a second generation structural analog of prostacyclin (PGI) with about ten-fold greater potency than the first generation stable analogs, such as carbaprostacyclin. Iloprost binds with equal affinity to human prostacyclin (Prostanoid IP) and prostaglandin EP1 receptors. Iloprost constricts the ilium and fundus circular smooth muscle as strongly as prostaglandin E2 (PGE2) itself. Iloprost inhibits the ADP, thrombin, and collagen-induced aggregation of human platelets. In whole animals, iloprost acts as a vasodilator, hypotensive, antidiuretic, and prolongs bleeding time. All of these properties help to antagonize the pathological changes that take place in the small pulmonary arteries of patients with pulmonary hypertension.
Phenacyl 5-[(3aR,4S,5R,6aR)-5-hydroxy-4-[(3R,4S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-3,3a,4,5,6,6a-hexahydro-1H-pentalen-2-ylidene]pentanoate
Gutierrezianolic acid 3-phenylpropionate methyl ester
3-Geranyl-4,2,4,6-tetrahydroxy-5-prenyldihydrochalcone
fischelactone|rel-(1aR,5S,5aR,9aR,9bR)-2,3,4,5,5a,6,9a,9b-octahydro-5,5a,7-trimethyl-9a-[(4aR,5S,9aS)-4,4a,5,6,7,8-hexahydro-3,4a,5-trimethyl-2-oxonaphtho[2,3-b]furan-9a(2H)-yl]-8H-oxireno[1,8a]naphtho[2,3-b]furan-8-one
ent-15beta-hydroxy-7alpha-(E)-lachnophylloyloxykaur-16-en-19-oic acid
2,4,6,4-tetrahydroxy-3-geranyl-3-prenyl-dihydrochalcone|dihydrochalcone M-1
bipinnatone A
A member of the class of dihydrochalones that is dihydrochalcone hydroxylated at C-2, C-4, C-6 and C-4 and substituted by a farnesyl group at C-3. It is isolated from the aerial parts of Boronia bipinnata and exhibits antimalarial activity.
methyl-3alpha-cinnamoyloxy-9beta-hydroxy-ent-kaurenoate
(2S)-2,3,9,10-tetrahydro-2-[3,4-dihydro-8-(3-hydroxy-3-methylbutyl)-2,2-dimethyl-2H-chromen-6-yl]-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one|tonkinochromane D
schweinfurthin F
A stilbenoid isolated from Macaranga alnifolia and has been shown to exhibit cytotoxic activity.