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Formula: C31H29ClN6O3S
Smiles: OC1=CC(O)=CC2O[C@@H]([C@@H](CC1=2)OC(=O)C1C=C(O)C(O)=C(O)C=1)C1C=C(O)C(O)=C(O)C=1
2-D08 also inhibits Axl with an IC50 of 0
3R)-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-2-[[2-[[(2S)-2-[[2-[[(2S)-2-[[2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-hydroxypropanoyl]amino]-3-phenylpropanoyl]amino]-5-carbamimidamidopentanoyl]amino]-4-oxobutanoyl]amino]acetyl]amino]-3-methylbutanoyl]amino]acetyl]amino]-3-hydroxypropanoyl]amino]acetyl]amino]-3-methylbutanoyl]amino]hexanoyl]amino]hexanoyl]amino]-3-hydroxybutanoyl]amino]-3-hydroxypropanoyl]amino]-3-phenylpropanoyl]amino]-5-carbamimidamidopentanoyl]amino]-5-carbamimidamidopentanoyl]amino]propanoyl]amino]hexanoyl]amino]-5-oxopentanoic acid 2
924473-59-6
Taccalonolide AJ Size:Contact [email protected] for quotation Formula: C31H29ClN6O3STaccalonolide AJ is a semi synthesis compound with cellular microtubule stabilizing activity. Taccalonolide AJ exhibits high potency antiproliferative activity against cancer cells, with an IC50 of 4. 2 nM for HeLa cells. Product information CAS Number: 1349904 82 0 Molecular Weight: 676. 70 Formula: C34H44O14 Chemical Name: (1S,2S,3R,5S,7S,9S,10R,11R,12S,13S,14R,15R,16S,17S,18S,20S,23S,24S,25R,26R) 13,14 bis(acetyloxy) 3,23,26 trihydroxy
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