HIV Protease Substrate VII

cas: 128340-45-4 — see every product listed under this CAS number, including other names

HIV Protease Substrate VII (CAS 128340-45-4) is a chemical reagent available from Chemat. Available pack sizes: on request, 1000ug, 2000ug, 5000ug. Offered by: Creative Peptides, Biosynth.

brandCreative Peptides
catalog numberCP-HB00143
cas128340-45-4
sizeon request
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Available pack sizes

brand size price
Creative Peptides on request price on request
Biosynth 1000ug price on request
Biosynth 2000ug price on request
Biosynth 5000ug price on request

properties

purityNo data
delivery timeTo be confirmed by Chemat
Structural formula: {0} (CAS {1})

(4S)-5-[[(2S)-1-[[(2S)-1-amino-1-oxohexan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2,6-diaminohexanoyl]amino]propanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-nitrophenyl)propanoyl]amino]-5-oxopentanoic acid (CAS 128340-45-4) is a chemical compound with the molecular formula C52H81N15O14 and a molecular weight of 1140.3 g/mol. IUPAC name: (4S)-5-[[(2S)-1-[[(2S)-1-amino-1-oxohexan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2,6-diaminohexanoyl]amino]propanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-nitrophenyl)propanoyl]amino]-5-oxopentanoic acid. InChIKey: SZTXMADWAUFULI-GOMXOUEZSA-N.

Identity
Molecular formulaC52H81N15O14
Molecular weight1140.3 g/mol
IUPAC name(4S)-5-[[(2S)-1-[[(2S)-1-amino-1-oxohexan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2,6-diaminohexanoyl]amino]propanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-nitrophenyl)propanoyl]amino]-5-oxopentanoic acid
InChIKeySZTXMADWAUFULI-GOMXOUEZSA-N
SMILESCCCC[C@@H](C(=O)N)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC1=CC=C(C=C1)[N+](=O)[O-])NC(=O)[C@H](CC2=CC=C(C=C2)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)N

Computed by PubChem (NCBI)