132-66-1
Chemical Structure
N-1-Naphthylphthalamic acid
Synonym(s): Alanap 1
- CAS No.: 132-66-1
- Formula:C18H13NO3
- Molecular Weight:291.31
IUPAC Name: 2-(naphthalen-1-ylcarbamoyl)benzoic acid
InChIKey: JXTHEWSKYLZVJC-UHFFFAOYSA-N
SMILES: O=C(C1=CC=CC=C1C(NC2=C3C=CC=CC3=CC=C2)=O)O
Biological Activity: N-1-Naphthylphthalamic acid (Alanap 1) is a modulator of polar auxin transport that competes with auxin (indole-3-acetic acid, IAA) for membrane binding sites. N-1-Naphthylphthalamic acid also disrupts maize leaf initiation, KNOX protein regulation, and leaf margin formation[1][1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N-1-Naphthylphthalamic acid | 99.97% | N-1-Naphthylphthalamic acid (Alanap 1) is a modulator of polar auxin transport that competes with auxin (indole-3-acetic acid, IAA) for membrane binding sites. N-1-Naphthylphthalamic acid also disrupts maize leaf initiation, KNOX protein regulation, and leaf margin formation. | ||||||||||||||||||||
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N-1-Naphthylphthalamic acid (Standard) | 98.55% | N-1-Naphthylphthalamic acid (Standard) is the analytical standard of N-1-Naphthylphthalamic acid. This product is intended for research and analytical applications. N-1-Naphthylphthalamic acid (Alanap 1) is a modulator of polar auxin transport that competes with auxin (indole-3-acetic acid, IAA) for membrane binding sites. N-1-Naphthylphthalamic acid also disrupts maize leaf initiation, KNOX protein regulation, and leaf margin formation. | ||||||||||||||||||||
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- [1]. Ihsan BurakCam, et al. Physical and chemical properties of cow cockle seeds (Vaccaria hispanica (Mill.) Rauschert) genetic resources of Turkey.
- [2]. Sussman MR, et al. The action of specific inhibitors of auxin transport on uptake of auxin and binding of N-1-naphthylphthalamic acid to a membrane site in maize coleoptiles. Planta. 1981 May;152(1):13-8. [Content Brief]