Azetidine-3-carboxylic acid
Azetidine-3-carboxylic acid
Résumé du produit
Aperçu rapide
- Famille de produits
- ADC Linkers & Conjugation Reagents
- Nom chimique
- Azetidine-3-carboxylic acid
- FM
- C4H7NO2
- PM
- 101.1
Azetidine-3-carboxylic acid is a small azetidine carboxylic acid identified by CAS 36476-78-5.
This record matches molecular formula C4H7NO2, molecular weight about 101.1, PubChem CID 93192, and InChIKey GFZWHAAOIVMHOI-UHFFFAOYSA-N.
The PubChem IUPAC name is azetidine-3-carboxylic acid.
Identité et spécifications
| Catalog No. | CH53012 |
| CAS No. | 36476-78-5 |
| Chemical Name | Azetidine-3-carboxylic acid |
| Molecular Formula | C4H7NO2 |
| Molecular Weight | 101.1 |
| PubChem CID | 93192 |
| InChIKey | GFZWHAAOIVMHOI-UHFFFAOYSA-N |
Contexte d’application
- Azetidine building-block identity: supports matching the azetidine carboxylic acid name with CAS 36476-78-5 and PubChem CID 93192.
- Catalog data alignment: useful when formula, molecular weight, CAS number, and InChIKey need to be checked together.
- Small heterocycle reference: provides a concise identity record for azetidine-3-carboxylic acid.
Informations complémentaires sur le matériau
Utilisations
Useful for aligning Azetidine-3-carboxylic acid with CAS 36476-78-5, formula C4H7NO2, PubChem CID 93192, and the InChIKey GFZWHAAOIVMHOI-UHFFFAOYSA-N.
Caractéristiques
- Small nitrogen heterocycle bearing a carboxylic acid group at the 3-position.
- CAS and product-name lookups both resolve to PubChem CID 93192.
- The formula and molecular weight align between CHEMOS source data and PubChem.
Ressources techniques associées
Chimie des espaceurs et charges utiles pour ADC
Espaceurs clivables ou stables, segments hydrophiles, fonctions réactives sélectives et intermédiaires espaceur-charge utile.
espaceurs ADC clivables vs non clivables
Comparer espèce libérée, déclencheur, stabilité en circulation, traitement cellulaire, charge, conjugaison et preuves analytiques.
Sources publiques
- 3-azetidinecarboxylic Acid | PubChem CID 93192
- Development of Solid-Phase Site-Specific Conjugation and Its Application toward Generation of Dual Labeled Antibody and Fab Drug Conjugates
Bioconjugate Chemistry, 2016
Product-family technical context
- Effect of Linker-Drug Properties and Conjugation Site on the Physical Stability of ADCs
Journal of Pharmaceutical Sciences, 2020
Product-family technical context
- Antibody-Maytansinoid Conjugates Are Activated in Targeted Cancer Cells by Lysosomal Degradation and Linker-Dependent Intracellular Processing
Cancer Research, 2006
Product-family technical context
- The Effect of Different Linkers on Target Cell Catabolism and Pharmacokinetics/Pharmacodynamics of Trastuzumab Maytansinoid Conjugates
Molecular Cancer Therapeutics, 2012
Product-family technical context
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