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Structure of Safranal
CAS No.: 116-26-7
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Safranal is the main active component of saffron, exhibiting neuroprotective and anti-inflammatory effects, particularly showing potential therapeutic value in research on neurodegenerative diseases such as Parkinson's disease.
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Batch number can be found on the product's label following the word 'Batch'.
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CAS No. : | 116-26-7 |
Formula : | C10H14O |
M.W : | 150.22 |
SMILES Code : | O=CC1=C(C)C=CCC1(C)C |
MDL No. : | MFCD00209531 |
InChI Key : | SGAWOGXMMPSZPB-UHFFFAOYSA-N |
Pubchem ID : | 61041 |
GHS Pictogram: |
![]() ![]() |
Signal Word: | Danger |
Hazard Statements: | H225-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Class: | 3 |
UN#: | 1993 |
Packing Group: | Ⅲ |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Rat neural stem cells (NSC) | 1, 20, or 100 ng/mL | 1 week | SAF at 20 and 100 ng/mL significantly increased TH and DAT positive rates and promoted dopamine release. | PMC6201804 |
HepG2 cells | 1, 0.3, 0.1, 0.03, 0.01 mM | 24 hours | To evaluate the effect of Safranal on HepG2 cell viability. Results showed that Safranal significantly reduced HepG2 cell viability in a dose-dependent manner, with almost 70% reduction at 1 mM concentration. | PMC8845597 |
Bone marrow-derived mast cells (BMMCs) | 10 µM or 100 µM | 24 hours | To investigate the inhibitory effect of Safranal on degranulation and inflammatory mediator production in BMMCs. Results showed that Safranal significantly reduced the release of β-hexosaminidase and inhibited the production of IL-6, TNF-α, and LTC4. | PMC8173045 |
Escherichia coli αR283D mutant | 12 mM | 60 minutes | Safranal partially inhibited αR283D mutant ATP synthase | PMC5884629 |
Escherichia coli wild-type | 8 mM | 60 minutes | Safranal fully inhibited wild-type F1Fo ATP synthase | PMC5884629 |
Bone marrow-derived macrophages (BMDMs) | 10 or 50 µM | 24 hours | To evaluate the cytotoxicity of Safranal in BMDMs and inhibit the production of NO, iNOS, and COX-2. | PMC6838343 |
RAW264.7 cells | 10 or 50 µM | 24 hours | To evaluate the cytotoxicity of Safranal in RAW264.7 cells and inhibit the production of NO, iNOS, and COX-2. | PMC6838343 |
HepG2 cells | 30–100 μM | 24 hours | To assess the effects of safranal on the survival of HepG2 cells. Results showed that safranal inhibited colony formation in a dose-dependent manner, being most effective at 100 µM dose. | PMC6240095 |
HepG2 cells | 50–900 μM | 24, 48, 72 hours | To assess the cytotoxic effects of safranal on HepG2 cells. Results showed that safranal inhibited cellular viability in a dose- and time-dependent manner (IC50 500 μM). | PMC6240095 |
HepG2 cells | 1, 0.7, 0.5 mM | 48 hours | To evaluate the effect of Safranal on caspase-3 and -7 activities in HepG2 cells. Results showed that Safranal significantly increased caspase-3 and -7 activities at 1 mM concentration. | PMC8845597 |
Human retinal microvascular endothelial cells (HRMECs) | 80 μg/mL | 5 days | Safranal protected HRMECs from high glucose-induced cell proliferation inhibition, reduced apoptosis, and inhibited cell migration and tube formation. | PMC9708741 |
HepG2 cells | 500 μM | 6–48 hours | To investigate how safranal affects cell cycle progression. Results showed that safranal caused G2/M phase arrest at 6 and 12 h post treatment, S-phase arrest at 24 h, and a significant (p < 0.001) increase in sub-G1 population post 24 and 48 h of treatment, indicating apoptosis induction. | PMC6240095 |
Rat aortic rings | 0.01–1 μM | To investigate the vasodilatory effect of Safranal on phenylephrine-precontracted aortic rings, results showed that Safranal caused vasodilation in both endothelium-intact and endothelium-denuded aortic rings. | PMC9268204 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Wistar rats | DEN/2-AAF-induced liver cancer model | Oral | 0.025 ml/kg and 0.05 ml/kg | Daily administration for 12 weeks | To evaluate the preventive effect of Safranal on DEN/2-AAF-induced liver cancer model. Results showed that Safranal significantly inhibited the formation of pre-neoplastic lesions, reduced the number and area of GST-p-positive foci, inhibited cell proliferation (Ki-67), induced apoptosis (TUNEL and M30 CytoDeath), and exhibited anti-inflammatory properties (inhibition of NF-kB, COX2, iNOS, TNF-alpha, and its receptor). | PMC8845597 |
BALB/c mice | OVA-induced asthma model and passive systemic anaphylaxis (PSA) model | Oral | 200 mg/kg or 500 mg/kg | Once daily for 7 days | To evaluate the anti-allergic effects of Safranal in OVA-induced asthma model and PSA model. Results showed that Safranal significantly reduced serum IgE levels, decreased mast cell infiltration in lung tissue, and balanced Th1/Th2 cytokine levels. In the PSA model, Safranal reduced the levels of histamine and LTC4 in serum. | PMC8173045 |
BALB/c mice | DSS-induced colitis model | Oral | 200 mg/kg or 500 mg/kg | Once daily for 7 days | To evaluate the clinical and histological effects of Safranal in DSS-induced colitis mice. | PMC6838343 |
C57BL/6J mice | Pentobarbital-treated mice model | Intragastrically | 90, 180, or 360 mg/kg | Single administration, observed for 3 hours | Safranal increased the duration of non-rapid eye movement (NREM) sleep, shortened NREM sleep latency, and enhanced the delta power activity of NREM sleep. Immunohistochemical evaluation revealed that safranal increased c-Fos expression in the ventrolateral preoptic nucleus (VLPO), one of the putative sleep centers, and decreased it in the arousal histaminergic tuberomammillary nuclei (TMN). | PMC6493539 |
Sprague-Dawley rats | 6-OHDA-induced Parkinson's disease model | Intrastriatal injection | 2 μL (100 ng/mL) | 2 and 4 weeks after transplantation | Transplantation of SAF-treated NSC significantly reduced rotation numbers, increased survival rates, and promoted the differentiation and survival of dopaminergic neurons. | PMC6201804 |
Tags: Safranal | Keap1-Nrf2 | Saffron | neuroprotective | antioxidant | anti-inflammatory | neuroprotective | Alzheimer's disease | Parkinson's disease | anticancer | antidepressant | 116-26-7
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