WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 403010

CAS#: 925705-73-3

Description: TG100713 is an inhibitor of PI3-kinase that inhibits endothelial cell proliferation.

Chemical Structure

CAS# 925705-73-3

Theoretical Analysis

MedKoo Cat#: 403010
Name: TG100713
CAS#: 925705-73-3
Chemical Formula: C12H10N6O
Exact Mass: 254.09161
Molecular Weight: 254.25
Elemental Analysis: C, 56.69; H, 3.96; N, 33.05; O, 6.29

Price and Availability

Size Price Availability Quantity
5.0mg USD 300.0 2 Weeks
10.0mg USD 550.0 2 Weeks
25.0mg USD 900.0 2 Weeks
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Synonym: TG100713; TG 100713; TG-100713

IUPAC/Chemical Name: 3-(2,4-diaminopteridin-6-yl)phenol


InChi Code: InChI=1S/C12H10N6O/c13-10-9-11(18-12(14)17-10)15-5-8(16-9)6-2-1-3-7(19)4-6/h1-5,19H,(H4,13,14,15,17,18)

SMILES Code: OC1=CC=CC(C2=NC3=C(N)N=C(N)N=C3N=C2)=C1

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO, not in water

Shelf Life: >5 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

Preparing Stock Solutions

The following data is based on the product molecular weight 254.25 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL

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 1. Doukas, J., Wrasidlo, W., Noronha, G., et al. Phosphoinositide 3-kinase γ/δ inhibition limits infarct size after myocardial ischemia/reperfusion injury. Proc. Natl. Acad. Sci. USA 103(52), 19866-19871 (2006).

2. Vargas, B., Giacobbi, N.S., Sanyal, A., et al. Inhibitors of signaling pathways that block reversal of HIV-1 latency. Antimicrob. Agents Chemother. 63(2), e01744-01718 (2019).

Additional Information