TNP-470

TNP-470
Names
	Preferred IUPAC name [(3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-yl] N-(2-chloroacetyl)carbamate
	Other names TNP-470, O-(chloroacetylcarbamoyl)fumagillol
Identifiers
CAS Number	129298-91-5;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:90748;
ChEMBL	ChEMBL424278;
ChemSpider	328427;
DrugBank	DB08633;
ECHA InfoCard	100.189.666
EC Number	663-348-8;
PubChem CID	369976;
UNII	X47GR46481;
CompTox Dashboard (EPA)	DTXSID0041141 ;
	InChI InChI=1S/C19H28ClNO6/c1-11(2)5-6-13-18(3,27-13)16-15(24-4)12(7-8-19(16)10-25-19)26-17(23)21-14(22)9-20/h5,12-13,15-16H,6-10H2,1-4H3,(H,21,22,23)/t12-,13-,15-,16-,18+,19+/m1/s1 Key: MSHZHSPISPJWHW-PVDLLORBSA-N;
	SMILES CC(=CC[C@@H]1[C@@](O1)(C)[C@H]2[C@@H]([C@@H](CC[C@]23CO3)OC(=O)NC(=O)CCl)OC)C;
Properties
Chemical formula	C19H28ClNO6
Molar mass	401.88 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

TNP-470 is an methionine aminopeptidase 2 inhibitor. Although it was one of the first angiogenesis inhibitor tested in clinical trials, its potential was hampered by neurotoxic effects and lack of effectiveness.^[1]^[2]^[3]

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