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Transketolase-IN-4
CAS No. 419547-73-2
Transketolase-IN-4( —— )
Catalog No. M36468 CAS No. 419547-73-2
Transketolase-IN-4 is a transketolase inhibitor with an IC50 value of 3.9 μM.Transketolase-IN-4 inhibited Mycobacterium tuberculosis DXS with an IC50 value of 114.1 μM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 33 | In Stock |
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| 5MG | 29 | In Stock |
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| 10MG | 50 | In Stock |
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| 25MG | 103 | In Stock |
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| 50MG | 152 | In Stock |
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| 100MG | 230 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameTransketolase-IN-4
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NoteResearch use only, not for human use.
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Brief DescriptionTransketolase-IN-4 is a transketolase inhibitor with an IC50 value of 3.9 μM.Transketolase-IN-4 inhibited Mycobacterium tuberculosis DXS with an IC50 value of 114.1 μM.
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DescriptionTransketolase-IN-4 is a potent transketolase inhibitor (IC50=3.9 μM). Transketolase-IN-4 inhibits tumor cell proliferation of SW620, LS174T, and MIA PaCa-2. Transketolase-IN-4 is a possible Mycobacterium tuberculosis DXS inhibitor, with an IC50 value of 114.1 μM.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorTransketolase | Antibacterial
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Research Area——
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Indication——
Chemical Information
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CAS Number419547-73-2
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Formula Weight335.79
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Molecular FormulaC19H14ClN3O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (372.26 mM; Ultrasonic )
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SMILESO=C1N2C(=C(C=N2)C3=CC=C(Cl)C=C3)NC(CC4=CC=CC=C4)=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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12-Dipalmitoyl-sn-gl...
12-Dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) a phospholipid member of the glycerophosphonoethanolamine family is a major component in biological membranes. Studies focused on interactions between DPPE and cholesterol show that cholesterol induces condensation of DPPE monolayers in the presence of Ca2+ ions.
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(E)-SI-2
(E)-SI-2 is a potent small-molecule inhibitor of steroid receptor coactivator-3 (SRC-3 or AIB1) that can selectively inhibit the intrinsic transcriptional activities of SRC-3, also inhibits SRC-1 and SRC-2.
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Isoangustone A
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation by targeting PI3K, MKK4, and MKK7 in human melanoma.
