178762-28-2
178762-28-2
Chemical Structure
Jineol
Synonym(s): 3,8-Quinolinediol
- CAS No.: 178762-28-2
- Formula:C9H7NO2
- Molecular Weight:161.16
IUPAC Name: quinoline-3,8-diol
InChIKey: IGDFDIZIHMFYGR-UHFFFAOYSA-N
SMILES: OC1=CC2=CC=CC(O)=C2N=C1
Biological Activity: Jineol is a cytotoxic alkaloid from the centipede Scolopendra subspinipes. Jineol exhibits modest cytotoxic activity in vitro against the growth of human tumor cell lines[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Jineol | 99.68% | Jineol is a cytotoxic alkaloid from the centipede Scolopendra subspinipes. Jineol exhibits modest cytotoxic activity in vitro against the growth of human tumor cell lines. | ||||||||||||||||||||
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1,2-Dihydroxynaphthalene | 98.88% | 1,2-Dihydroxynaphthalene is a metabolic intermediate of Naphthalene and a precursor for the formation of 1,2-Naphthoquinone, and is also the most sensitive biomarker of Naphthalene exposure in humans. 1,2-Dihydroxynaphthalene inhibits the AMPK/SIRT3 pathway and activates acetylated p53 and NF-κB by inducing oxidative stress, leading to G2/M cell cycle arrest, senescence, and apoptosis, while also damaging DNA through the formation of depurination adducts, thereby causing mutations. 1,2-Dihydroxynaphthalene can be used in research on cancer and cataracts. | ||||||||||||||||||||
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Cloxiquine | 99.94% | Cloxiquine (5-Chloro-8-quinolinol) is an antibacterial, antifungal and antiamoebic agent. Cloxiquine can be used for the research of tuberculosis and dermatoses. Cloxiquine suppresses the growth and metastasis of melanoma cells through activation of PPARγ. | ||||||||||||||||||||
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8-Hydroxyquinoline | 99.95% | 8-Hydroxyquinoline (8-Quinolinol) is a lipophilic metal chelator that can be used as a fungicide .8-Hydroxyquinoline shows the MIC range of 27.56-55.11 μM (4-8 μg/mL) against the clinical isolates of Neisseria gonorrhoeae. 8-Hydroxyquinoline can bind to copper form complexes and transport copper into cells. 8-Hydroxyquinoline increases in the number of micronucleated polychromatic erythrocytes and can also make hair depigmented in mice. | ||||||||||||||||||||
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Naphthoresorcinol | 99.49% | Naphthoresorcinol (1,3-Dihydroxynaphthalene) is a fluorescent dye (λex=330 nm, λem=380 nm) that can react with the NPPD (a tracer) and concentrated HCl and develop a red color. Naphthoresorcinol could be used as a background electrolyte (BGE) to determine the carbohydrates. | ||||||||||||||||||||
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5-Amino-8-hydroxyquinoline | 95.0% | 5-Amino-8-hydroxyquinoline (5A8HQ; 5AHQ) is an orally active non-competitive 20S proteasome inhibitor. 5-Amino-8-hydroxyquinoline can inhibit NF-κB activity and induce cancer cells death and shows low cytotoxicity towards normal hematopoietic cells. 5-Amino-8-hydroxyquinoline can be used for the research of cancer, such as leukemia. | ||||||||||||||||||||
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2,3-Dihydroxynaphthalene | 98.62% | Naphthalene-2,3-diol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2,7-Dihydroxynaphthalene (Standard) | ≥98% | 2,7-Dihydroxynaphthalene (Standard) (2,7-DHN (Standard)) is the analytical standard of 2,7-Dihydroxynaphthalene (HY-W015451). This product is intended for research and analytical applications. 2,7-Dihydroxynaphthalene (2,7-DHN) is a substrate of a new group of aromatic prenyltransferases in fungi and can be catalyzed to undergo a regiospecific prenylation reaction. 2,7-Dihydroxynaphthalene can undergo reactions such as oxidation and substitution. | ||||||||||||||||||||
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Tiliquinol | 99.55% | Tiliquinol (NSC 130828) is a non-absorbed anti-amoebic luminal agent. Tiliquinol is used in combination with tibroquinol. Tiliquinol can be used for the research of amebic liver abscess. | ||||||||||||||||||||
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4,6-Dihydroxyquinoline | 98.15% | 4,6-Dihydroxyquinoline is an oxidation product of 5-hydroxykynuramine. | ||||||||||||||||||||
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4-Chloroquinolin-8-ol | 4-Chloroquinolin-8-ol (compound 1) is an Alq3-derived aluminum ligand. Alq3 is an organometallic molecule widely used as electron transport layer and light-emitting layer in organic LEDs, and also as a host for fluorescent and phosphorescent dyes. | |||||||||||||||||||||
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