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Fmoc-Dab (Boc) -OH

CAT: 0804-HY-W008024-01Size: 5 gDry Ice: NoHazardous: No
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CAT#:0804-HY-W008024-01Size:5 g
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Fmoc-Dab (Boc) -OH is an amino acid derivative with an Fmoc protecting group that can be used to synthesize somatostatin analogs that inhibit neointima formation induced by balloon injury in rats without altering growth hormone release. Fmoc-Dab (Boc) -OH can be used for the synthesis of peptides[1][2].
CAS Number
125238-99-5
UNSPSC
12352209
Hazard Statement
H302, H315, H319, H335
Target
Amino Acid Derivatives
Type
Peptides
Related Pathways
Others
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/fmoc-dab-boc-oh.html
Purity
99.78
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
O=C([C@H](CCNC(OC(C)(C)C)=O)NC(OCC1C2=C(C=CC=C2)C3=C1C=CC=C3)=O)O
Molecular Formula
C24H28N2O6
Molecular Weight
440.49
Precautions
H302, H315, H319, H335
References & Citations
[1]Thurieau, et al. "A new somatostatin analog with optimized ring size inhibits neointima formation induced by balloon injury in rats without altering growth hormone release." European journal of medicinal chemistry 30.2 (1995) : 115-122.|[2]García-Gros J, et al. Synthesis of the Antimicrobial Peptide Murepavadin Using Novel Coupling Agents. Biomolecules. 2024 Apr 27;14 (5) :526.
Shipping Conditions
Room Temperature
Storage Conditions
Store at room temperature 3 years
Scientific Category
Peptides
Clinical Information
No Development Reported

Chemical Information

(2S)-4-(((tert-butoxy)carbonyl)amino)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid
CAS Number125238-99-5
PubChem CID2756101
IUPAC Name(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
Molecular FormulaC24H28N2O6
Molecular Weight440.5
XLogP3.7
Topological Polar Surface Area114
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count10
Heavy Atom Count32
Formal Charge0
Complexity654
SMILES
CC(C)(C)OC(=O)NCC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChI
InChI=1S/C24H28N2O6/c1-24(2,3)32-22(29)25-13-12-20(21(27)28)26-23(30)31-14-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,19-20H,12-14H2,1-3H3,(H,25,29)(H,26,30)(H,27,28)/t20-/m0/s1
InChIKey
LIWKOFAHRLBNMG-FQEVSTJZSA-N
Chemical Structure
2D Structure
2D structure of (2S)-4-(((tert-butoxy)carbonyl)amino)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)butanoic acid
CAS: 125238-99-5
CID: 2756101
Formula: C24H28N2O6
MW: 440.5
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight440.5
XLogP33.7
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count10
Exact Mass440.19473662
Monoisotopic Mass440.19473662
Topological Polar Surface Area114 Ų
Heavy Atom Count32
Formal Charge0
Complexity654
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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CatalogName
5-04727Fmoc-Dab[Fmoc-Dab(Boc)]-OH
FF71806-01Fmoc-Dab (Fmoc-Dab (Boc) ) -OH
B-1800.0001Fmoc-Dab(Boc)-OH
A-3520.0005Boc-Dab(Fmoc)-OH
4016009.0001Fmoc-Dab (Boc) -OH
sc-223837Boc-Dab (Fmoc) -OH
4027507.0001Boc-D-Dab (Fmoc) -OH
MBS405106-01Fmoc-D-Dab(Boc)-OH
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