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Molecule
ID:103848
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₂₇N₇O₈
Molecular Mass
433.41698
Exact Mass
433.19211086
Charge
0
InChI
InChI=1S/C15H27N7O8/c16-7(2-1-3-19-15(17)18)12(27)20-5-10(24)21-8(4-11(25)26)13(28)22-9(6-23)14(29)30/h7-9,23H,1-6,16H2,(H,20,27)(H,21,24)(H,22,28)(H,25,26)(H,29,30)(H4,17,18,19)
InChIKey
NNRFRJQMBSBXGO-UHFFFAOYSA-N
Canonic Smiles
OCC(C(=O)O)NC(=O)C(CC(=O)O)NC(=O)CNC(=O)C(CCCNC(=N)N)N
Isomeric Smiles
NC(CCCNC(=N)N)C(=O)NCC(=O)NC(CC(=O)O)C(=O)NC(CO)C(=O)O
Calculated Properties
JChem
Acid pKa
-0.77673435
H Acceptors
12
H Donor
10
LogD (pH = 5.5)
-9.26485
LogD (pH = 7.4)
-9.405291
Log P
-9.266645
Molar Refractivity
108.9005
Polarizability
38.612175
Polar Surface Area
270.05
Rotatable Bonds
14
Lipinski's Rule of Five
false
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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IUPAC name
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IUPAC Traditional name
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PubChem SID
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PubChem CID
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MP Biomedicals
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02153053
Academic Data
PubChem
4649132
Names and Identifiers
IUPAC name
3-[2-(2-amino-5-carbamimidamidopentanamido)acetamido]-3-[(1-carboxy-2-hydroxyethyl)carbamoyl]propanoic acid
IUPAC Traditional name
3-[2-(2-amino-5-carbamimidamidopentanamido)acetamido]-3-[(1-carboxy-2-hydroxyethyl)carbamoyl]propanoic acid
Synonyms
ARG-GLY-ASP-SER
Registration numbers
CAS Number
91037-65-9
PubChem SID
162103017
PubChem CID
4649132
Properties
Safety Information
MSDS Link
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Source
Storage Condition
-20°C
Source
Product Information
Certificate of Analysis
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Molecule Details
MP Biomedicals
02153053
Supports fibroblast attachment and inhibits fibronectin binding to platelets.
A target sequence for syphilis spirochete cytadherence.
References
PubChem Literature
From Data Sources
•
Pierschbacher, M.D. and Ruoslahti, E., Nature, 309: 30, (1984).
Bioactivity
PubChem BioAssay