5-L-Valineangiotensin II acetate

cas: 5649-07-0 — see every product listed under this CAS number, including other names

5-L-Valineangiotensin II acetate (CAS 5649-07-0) is a chemical reagent available from Chemat. Available pack sizes: 5mg, 25mg, 100mg, 500mg. Offered by: Chemat.

brandChemat
catalog numberCh11E0VT-5mg
cas5649-07-0
size5mg
availability 0.5g
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Available pack sizes

brand size price
Chemat 5mg 208.40 Pln
Chemat 25mg 530.00 Pln
Chemat 100mg 1274.00 Pln
Chemat 500mg 5171.60 Pln

properties

delivery time3 weeks
Structural formula: {0} (CAS {1})

Acetic acid;(3S)-3-amino-4-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[(2S)-2-[[(1S)-1-carboxy-2-phenylethyl]carbamoyl]pyrrolidin-1-yl]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-oxobutanoic acid (CAS 5649-07-0) is a chemical compound with the molecular formula C51H73N13O14 and a molecular weight of 1092.2 g/mol. IUPAC name: acetic acid;(3S)-3-amino-4-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[(2S)-2-[[(1S)-1-carboxy-2-phenylethyl]carbamoyl]pyrrolidin-1-yl]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-oxobutanoic acid. InChIKey: JVCJXRGXGITABA-IAQGTVMASA-N.

Identity
Molecular formulaC51H73N13O14
Molecular weight1092.2 g/mol
IUPAC nameacetic acid;(3S)-3-amino-4-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[(2S)-2-[[(1S)-1-carboxy-2-phenylethyl]carbamoyl]pyrrolidin-1-yl]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-oxobutanoic acid
InChIKeyJVCJXRGXGITABA-IAQGTVMASA-N
SMILESCC(C)[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC2=CN=CN2)C(=O)N3CCC[C@H]3C(=O)N[C@@H](CC4=CC=CC=C4)C(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(=O)O)N.CC(=O)O

Computed by PubChem (NCBI)

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