| Identification | Back Directory | [Name]
TG 100713 | [CAS]
925705-73-3 | [Synonyms]
CS-577
TG100110
TG 100713
TG100713;TG 100713
TG 100713 USP/EP/BP
3-(2,4-Diaminopteridin-6-yl)phenol
3-(2,4-DiaMino-6-pteridinyl)phenol
Phenol, 3-(2,4-diamino-6-pteridinyl)-
TG 100713,3-(2,4-DiaMino-6-pteridinyl)-phenol | [Molecular Formula]
C12H10N6O | [MDL Number]
MFCD20926347 | [MOL File]
925705-73-3.mol | [Molecular Weight]
254.25 |
| Hazard Information | Back Directory | [Uses]
TG 100713 is an inhibitor of PI3-kinase. TG 100713 inhibits endothelial cell proliferation. | [Biological Activity]
tg100713 is a pan-pi3k inhibitor against pi3kγ, pi3kδ, pi3kα and pi3kβ.pi3kγ and pi3kδ are a pair of pro-inflammatory pi3k isoforms that contribute to the inflammation that damages ischemia tissues upon reperfusion. phosphoinositide 3-kinases (pi3ks) are benefit to pro-cell survival roles during tissue iscg the reperfusion phhemia. therefore, it is possible that selectively inhibiting pro-inflammatory pi3k isoforms durinase could ultimately control overall tissue damage caused by ischemia/reperfusion injuries such as myocardial infarction. | [in vitro]
modeling studies suggested that the freedom of conformational rotation permitted by ring substituents controls isoform selectivity. although substituent ring of tg100-115, tg100713, and tg101110 all require energy minima at 30–40°, angles diverge of each compound results in paying differing penalties from this range. tg100-115 displays the greatest barrier to rotation and finally is the most isoform selective, tg100713 has the most conformational flexibility (ring a being almost freely rotatable with maxima ≈5 kcal; 1 kcal = 4.18 kj), suggesting the least selective, and tg101110 lies an intermediate position (several conformations ≦10 but some >>50 kcal) [1]. | [in vivo]
the minimum structure which satisfies all three requirements is shown in tg100713, which so far has also displayed the best pi3k binding activity. interestingly, the sar profiles generating correlate quite well with the results of the initial in vivo screen further supports the involvement of pi3k as a target for inhibiting vascular permeability in related compounds [2]. | [IC 50]
(pi3kγ, pi3kδ, pi3kα and pi3kβ): 50 nm, 24 nm, 165 nm and 215 nm | [References]
[1] doukas j, wrasidlo w, noronha g, dneprovskaia e, fine r, weis s, hood j, demaria a, soll r, cheresh d. phosphoinositide 3-kinase gamma/delta inhibition limits infarct size after myocardial ischemia/reperfusion injury. proc natl acad sci u s a. 2006 dec 26; 103(52):19866-71.
[2] palanki ms, dneprovskaia e, doukas j, fine rm, hood j, kang x, lohse d, martin m, noronha g, soll rm, wrasidlo w, yee s, zhu h. discovery of 3,3'-(2,4-diaminopteridine-6,7-diyl)diphenol as an isozyme-selective inhibitor of pi3k for the treatment of ischemia reperfusion injury associated with myocardial infarction. j med chem. 2007 sep 6;50(18):4279-94. epub 2007 aug 9. |
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