Cholecystokinin Precursor (24-32) (rat)

cas: 99291-20-0 — see every product listed under this CAS number, including other names

Cholecystokinin Precursor (24-32) (rat) (CAS 99291-20-0) is a chemical reagent available from Chemat. Available pack sizes: on request, 10mg, 5mg, 25mg. Offered by: Creative Peptides, Biosynth.

brandCreative Peptides
catalog numberCP-C21042
cas99291-20-0
sizeon request
Need more information?

Ask us about this product — we're happy to help.

Available pack sizes

brand size price
Creative Peptides on request price on request
Biosynth 10mg price on request
Biosynth 5mg price on request
Biosynth 25mg price on request

properties

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

(4S)-4-[[(2S)-2-[[1-[(2S)-2-amino-3-methylbutanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-5-[[(2S)-1-[[(2S)-1-[[(2S)-3-carboxy-1-[(2S)-2-[[(1S)-1-carboxy-3-methylsulfanylpropyl]carbamoyl]pyrrolidin-1-yl]-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxopropan-2-yl]amino]-5-oxopentanoic acid (CAS 99291-20-0) is a chemical compound with the molecular formula C42H69N9O14S and a molecular weight of 956.1 g/mol. IUPAC name: (4S)-4-[[(2S)-2-[[1-[(2S)-2-amino-3-methylbutanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-5-[[(2S)-1-[[(2S)-1-[[(2S)-3-carboxy-1-[(2S)-2-[[(1S)-1-carboxy-3-methylsulfanylpropyl]carbamoyl]pyrrolidin-1-yl]-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxopropan-2-yl]amino]-5-oxopentanoic acid. InChIKey: AIKMAJWJXJPJNB-MHJJKFOESA-N.

Identity
Molecular formulaC42H69N9O14S
Molecular weight956.1 g/mol
IUPAC name(4S)-4-[[(2S)-2-[[1-[(2S)-2-amino-3-methylbutanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-5-[[(2S)-1-[[(2S)-1-[[(2S)-3-carboxy-1-[(2S)-2-[[(1S)-1-carboxy-3-methylsulfanylpropyl]carbamoyl]pyrrolidin-1-yl]-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
InChIKeyAIKMAJWJXJPJNB-MHJJKFOESA-N
SMILESC[C@@H](C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCSC)C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C(C)C)NC(=O)C2CCCN2C(=O)[C@H](C(C)C)N

Computed by PubChem (NCBI)

Also listed as