Substance P acetate salt

cas: 137348-11-9 — see every product listed under this CAS number, including other names

Substance P acetate salt (CAS 137348-11-9) is a chemical reagent available from Chemat. Available pack sizes: 10mg, 5mg, 25mg, 50mg, 100mg. Offered by: Biosynth.

brandBiosynth
catalog numberFS108549-10mg
cas137348-11-9
size10mg
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Available pack sizes

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properties

categoryLife Sciences
sub-category 1Peptides and Biochemicals
sub-category 2Research Peptides
purityNo data
delivery time1-2 weeks
Structural formula: {0} (CAS {1})

Acetic acid;2-[[1-[6-amino-2-[[1-[2-amino-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-N-[5-amino-1-[[1-[[1-[[2-[[1-[(1-amino-4-methylsulfanyl-1-oxobutan-2-yl)amino]-4-methyl-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1,5-dioxopentan-2-yl]pentanediamide (CAS 137348-11-9) is a chemical compound with the molecular formula C65H102N18O15S and a molecular weight of 1407.7 g/mol. IUPAC name: acetic acid;2-[[1-[6-amino-2-[[1-[2-amino-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-N-[5-amino-1-[[1-[[1-[[2-[[1-[(1-amino-4-methylsulfanyl-1-oxobutan-2-yl)amino]-4-methyl-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1,5-dioxopentan-2-yl]pentanediamide. InChIKey: ZVZBDDSODJLJBS-UHFFFAOYSA-N.

Identity
Molecular formulaC65H102N18O15S
Molecular weight1407.7 g/mol
IUPAC nameacetic acid;2-[[1-[6-amino-2-[[1-[2-amino-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-N-[5-amino-1-[[1-[[1-[[2-[[1-[(1-amino-4-methylsulfanyl-1-oxobutan-2-yl)amino]-4-methyl-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1,5-dioxopentan-2-yl]pentanediamide
InChIKeyZVZBDDSODJLJBS-UHFFFAOYSA-N
SMILESCC(C)CC(C(=O)NC(CCSC)C(=O)N)NC(=O)CNC(=O)C(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C(CCC(=O)N)NC(=O)C(CCC(=O)N)NC(=O)C3CCCN3C(=O)C(CCCCN)NC(=O)C4CCCN4C(=O)C(CCCN=C(N)N)N.CC(=O)O

Computed by PubChem (NCBI)

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