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7423-55-4,MFCD00043030
Catalog No.:AA0033NU

7423-55-4 | 3-Maleimidopropionic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$16.00   $12.00
- +
5g
95%
in stock  
$24.00   $17.00
- +
25g
95%
in stock  
$67.00   $47.00
- +
100g
95%
in stock  
$177.00   $124.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0033NU
Chemical Name:
3-Maleimidopropionic acid
CAS Number:
7423-55-4
Molecular Formula:
C7H7NO4
Molecular Weight:
169.1348
MDL Number:
MFCD00043030
SMILES:
OC(=O)CCN1C(=O)C=CC1=O
Properties
Properties
 
BP:
382.5 °C at 760 mmHg  
Form:
Solid  
MP:
103-106 °C  
Stability:
Moisture Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
251  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  

Literature

Title: Biophysical property and broad anti-HIV activity of albuvirtide, a 3-maleimimidopropionic acid-modified peptide fusion inhibitor.

Journal: PloS one 20120101

Title: Enhancing cellular uptake of activable cell-penetrating peptide-doxorubicin conjugate by enzymatic cleavage.

Journal: International journal of nanomedicine 20120101

Title: Albumin-conjugated C34 peptide HIV-1 fusion inhibitor: equipotent to C34 and T-20 in vitro with sustained activity in SCID-hu Thy/Liv mice.

Journal: The Journal of biological chemistry 20081205

Title: Protein and electrode engineering for the covalent immobilization of P450 BMP on gold.

Journal: Analytical chemistry 20081115

Title: Evaluation of low energy CID and ECD fragmentation behavior of mono-oxidized thio-ether bonds in peptides.

Journal: Journal of the American Society for Mass Spectrometry 20070301

Title: The use of poly(ethylene glycol)-block-poly(lactic acid) derived copolymers for the rapid creation of biomimetic surfaces.

Journal: Biomaterials 20031101

Title: An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562

Quotation Request
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SDS
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Tags:7423-55-4 Molecular Formula|7423-55-4 MDL|7423-55-4 SMILES|7423-55-4 3-Maleimidopropionic acid
Catalog No.: AA0033NU
7423-55-4,MFCD00043030
7423-55-4 | 3-Maleimidopropionic acid
Pack Size： 1g
Purity： 95%
in stock
$16.00 $12.00
Pack Size： 5g
Purity： 95%
in stock
$24.00 $17.00
Pack Size： 25g
Purity： 95%
in stock
$67.00 $47.00
Pack Size： 100g
Purity： 95%
in stock
$177.00 $124.00
Quantity
- +
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bulk Quotation Request
Technical Information
Catalog Number: AA0033NU
Chemical Name: 3-Maleimidopropionic acid
CAS Number: 7423-55-4
Molecular Formula: C7H7NO4
Molecular Weight: 169.1348
MDL Number: MFCD00043030
SMILES: OC(=O)CCN1C(=O)C=CC1=O
Properties
BP: 382.5 °C at 760 mmHg  
Form: Solid  
MP: 103-106 °C  
Stability: Moisture Sensitive  
Storage: Keep in dry area;Room Temperature;  
Complexity: 251  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
Literature fold

Title: Biophysical property and broad anti-HIV activity of albuvirtide, a 3-maleimimidopropionic acid-modified peptide fusion inhibitor.

Journal: PloS one20120101

Title: Enhancing cellular uptake of activable cell-penetrating peptide-doxorubicin conjugate by enzymatic cleavage.

Journal: International journal of nanomedicine20120101

Title: Albumin-conjugated C34 peptide HIV-1 fusion inhibitor: equipotent to C34 and T-20 in vitro with sustained activity in SCID-hu Thy/Liv mice.

Journal: The Journal of biological chemistry20081205

Title: Protein and electrode engineering for the covalent immobilization of P450 BMP on gold.

Journal: Analytical chemistry20081115

Title: Evaluation of low energy CID and ECD fragmentation behavior of mono-oxidized thio-ether bonds in peptides.

Journal: Journal of the American Society for Mass Spectrometry20070301

Title: The use of poly(ethylene glycol)-block-poly(lactic acid) derived copolymers for the rapid creation of biomimetic surfaces.

Journal: Biomaterials20031101

Title: An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562

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