HIV Protease Substrate IV

cas: 128340-47-6 — see every product listed under this CAS number, including other names

HIV Protease Substrate IV (CAS 128340-47-6) is a chemical reagent available from Chemat. Available pack sizes: on request, 1mg, 25mg, 5mg, 10mg, Get quote. Offered by: Creative Peptides, GLPBio, Biosynth, MedChemExpress.

brandCreative Peptides
catalog numberCP-HB00144
cas128340-47-6
sizeon request
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Available pack sizes

brand size price
Creative Peptides on request price on request
GLPBio 1mg 1336.56 Pln
GLPBio 25mg 7191.86 Pln
GLPBio 5mg 2487.96 Pln
Biosynth 10mg price on request
Biosynth 25mg price on request
MedChemExpress Get quote 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]hexanoyl]amino]-3-(4-nitrophenyl)propanoyl]amino]-5-oxopentanoic acid (CAS 128340-47-6) is a chemical compound with the molecular formula C49H83N15O13 and a molecular weight of 1090.3 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]hexanoyl]amino]-3-(4-nitrophenyl)propanoyl]amino]-5-oxopentanoic acid. InChIKey: MJGGTDHEIUOPEB-WBMHOGBOSA-N.

Identity
Molecular formulaC49H83N15O13
Molecular weight1090.3 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]hexanoyl]amino]-3-(4-nitrophenyl)propanoyl]amino]-5-oxopentanoic acid
InChIKeyMJGGTDHEIUOPEB-WBMHOGBOSA-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](CCCC)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)

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