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TG 100713

CAS No.
925705-73-3
Chemical Name:
TG 100713
Synonyms
CS-577;TG100110;TG 100713;TG100713;TG 100713;TG 100713 USP/EP/BP;TG100713 TG-100713 PI3K Inhibitor;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
CBNumber:
CB82550804
Molecular Formula:
C12H10N6O
Molecular Weight:
254.25
MDL Number:
MFCD20926347
MOL File:
925705-73-3.mol
Last updated:2023-05-21 10:59:17

TG 100713 Properties

storage temp. Store at -20°C
solubility Limited solubility, soluble in DMSO
form solid
color Yellow

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H315-H319-H335
Precautionary statements  P261-P280-P305+P351+P338

TG 100713 price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 30195 TG100713 925705-73-3 1mg $32 2024-03-01 Buy
Cayman Chemical 30195 TG100713 925705-73-3 25mg $420 2024-03-01 Buy
Cayman Chemical 30195 TG100713 925705-73-3 5mg $145 2024-03-01 Buy
Cayman Chemical 30195 TG100713 925705-73-3 10mg $184 2024-03-01 Buy
TRC T337800 TG100713 925705-73-3 10mg $160 2021-12-16 Buy
Product number Packaging Price Buy
30195 1mg $32 Buy
30195 25mg $420 Buy
30195 5mg $145 Buy
30195 10mg $184 Buy
T337800 10mg $160 Buy

TG 100713 Chemical Properties,Uses,Production

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.

TG 100713 Preparation Products And Raw materials

Raw materials

Preparation Products

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