536-60-7
Chemical Structure
4-Isopropylbenzyl alcohol
Synonym(s): Cuminic alcohol
- CAS No.: 536-60-7
- Formula:C10H14O
- Molecular Weight:150.22
IUPAC Name: (4-isopropylphenyl)methanol
InChIKey: OIGWAXDAPKFNCQ-UHFFFAOYSA-N
SMILES: OCC1=CC=C(C(C)C)C=C1
Biological Activity: 4-Isopropylbenzyl alcohol (Cuminic alcohol) is an opioid-dependent analgesic. 4-Isopropylbenzyl alcohol activates opioid receptor, regulates the L-Arginine (HY-N0455)/NO/cGMP pathway, and reduces spinal cord TNF-α and IL-1β levels; it binds to BSA (HY-D0842) via static quenching. 4-Isopropylbenzyl alcohol can be used in research related to nociceptive pain, neuropathic pain, bacterial infection and diabetes[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Isopropylbenzyl alcohol | 99.48% | 4-Isopropylbenzyl alcohol (Cuminic alcohol) is an opioid-dependent analgesic. 4-Isopropylbenzyl alcohol activates opioid receptor, regulates the L-Arginine (HY-N0455)/NO/cGMP pathway, and reduces spinal cord TNF-α and IL-1β levels; it binds to BSA (HY-D0842) via static quenching. 4-Isopropylbenzyl alcohol can be used in research related to nociceptive pain, neuropathic pain, bacterial infection and diabetes. | ||||||||||||||||||||
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4-Isopropylbenzyl alcohol (Standard) | ≥98% | (±)-Leucine (Standard) is the analytical standard of (±)-Leucine. This product is intended for research and analytical applications. (±)-Leucine (DL-Leucine), an isomer of Leucine, chemosterilant and dietary additive. (±)-Leucine inhibits growth of Escherichia coli HfrH by 92.08%. | ||||||||||||||||||||
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References
- [1]. Sheikholeslami MA, et al. Analgesic effects of cuminic alcohol (4-isopropylbenzyl alcohol), a monocyclic terpenoid, in animal models of nociceptive and neuropathic pain: Role of opioid receptors, L-arginine/NO/cGMP pathway, and inflammatory cytokines. European journal of pharmacology. 2021 Jun 05;900:174075.
- [2]. Ali MS, et al. Exploration of the binding between cuminol and bovine serum albumin through spectroscopic, molecular docking and molecular dynamics methods. Journal of biomolecular structure & dynamics. 2022;40(22):12404-12412.
