275-51-4
275-51-4
Chemical Structure
Azulene
Synonym(s): Cyclopentacycloheptene
- CAS No.: 275-51-4
- Formula:C10H8
- Molecular Weight:128.17
IUPAC Name: azulene
InChIKey: CUFNKYGDVFVPHO-UHFFFAOYSA-N
SMILES: C12=CC=CC=CC1=CC=C2
Biological Activity: Azulene (Cyclopentacycloheptene) is as an isomer of naphthalene with high anti-HIV activity. Azulene, isolated from the distillation of chamomile oil, is a scaffold in medicinal chemistry[1][2][3].
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Azulene | 99.97% | Azulene (Cyclopentacycloheptene) is as an isomer of naphthalene with high anti-HIV activity. Azulene, isolated from the distillation of chamomile oil, is a scaffold in medicinal chemistry. | ||||||||||||||||||||
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Azulene (Standard) | ≥98% | Azulene (Standard) is the analytical standard of Azulene. This product is intended for research and analytical applications. Azulene (Cyclopentacycloheptene) is as an isomer of naphthalene with high anti-HIV activity. Azulene, isolated from the distillation of chamomile oil, is a scaffold in medicinal chemistry. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.86
HY-W777535Naphthalene-13C10 -
Similarity Score 0.86
HY-W777535SNaphthalene-sup>13C6 -
Similarity Score 0.80
HY-W0080303-Aminobiphenyl -
Similarity Score 0.80
HY-W0170774-Methylbiphenyl -
Similarity Score 0.80
HY-W0169833-Phenylphenol -
Similarity Score 0.79
HY-W1402083-Phenylthiophene -
Similarity Score 0.78
![[1,1'-Biphenyl]-3-amine-<sup>13</sup>C<sub>6</sub> hydrochloride Chemical Structure](//file.medchemexpress.com/product_pic/hy-w106014s.gif)
HY-W106014S[1,1'-Biphenyl]-3-amine-13C6 hydrochloride -
Similarity Score 0.78
HY-418264-Bromobiphenyl -
Explore the MedChemAI to find more analogs
![[1,1'-Biphenyl]-3-amine-<sup>13</sup>C<sub>6</sub> hydrochloride Chemical Structure](http://file.medchemexpress.com/product_pic/hy-w106014s.gif)
References
- [1]. Teppo O Leino, et al. Azulene-based Compounds for Targeting Orexin Receptors. Eur J Med Chem. 2018 Sep 5;157:88-100. [Content Brief]
- [2]. Julia Peet, et al. Antiretroviral (HIV-1) Activity of Azulene Derivatives. Bioorg Med Chem. 2016 Apr 15;24(8):1653-7. [Content Brief]
- [3]. David A. Becker, et al. A new synthesis of substituted azulenes. Journal of the American Chemical Society, 111(1), 389-391.
