Patulitrin | CAS:19833-25-1 | Manufacturer ChemFaces

Patulitrin

Citing Use of our Products

How to Order

Orders via your E-mail:

1. Product number / Name / CAS No.
2. Delivery address
3. Ordering/billing address
4. Contact information
Sent to Email: info@chemfaces.com

Order & Inquiry & Tech Support

Tel: (0086)-27-84237683
Fax: (0086)-27-84254680
E-mail: manager@chemfaces.com
Address: No. 83, CheCheng Rd., WETDZ, Wuhan, Hubei 430056, PRC

Delivery time

Delivery & Payment method

1. Usually delivery time: Next day delivery by 9:00 a.m. Order now

2. We accept: Wire transfer & Credit card & Paypal & Western Union

* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.

According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.

Size /Price /Stock	10 mM * 1 mL in DMSO / $338 / In-stock
Other Packaging	*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap

Featured Products

Salviolone

Catalog No: CFN92163
CAS No: 119400-86-1
Price: $595/5mg

Quercetin-3-O-glucuronide

Catalog No: CFN92172
CAS No: 22688-79-5
Price: $298/20mg

Gomisin N

Catalog No: CFN90125
CAS No: 69176-52-9
Price: $268/20mg

Ganoderiol F

Catalog No: CFN99244
CAS No: 114567-47-4
Price: $398/5mg

Voacangine

Catalog No: CFN92252
CAS No: 510-22-5
Price: $463/5mg

Shikonin

Catalog No: CFN99907
CAS No: 517-88-4
Price: $80/20mg

N-trans-Feruloyltyramine

Catalog No: CFN97135
CAS No: 66648-43-9
Price: $288/10mg

Description:

Patulitrin has antioxidant, anti-inflammatory, and larvicidal activities, oral and topical administration of patuletin and patulitrin inhibited acute inflammation in mice.

Targets:

Antifection

In vitro:

Evid Based Complement Alternat Med. 2017;2017:9602368.

Larvicidal Activity against Aedes aegypti and Chemical Characterization of the Inflorescences of Tagetes patula.[Pubmed: 29362590 ]

METHODS AND RESULTS:
The crude acetone extract (CAE) of defatted inflorescences of Tagetes patula was partitioned into five semipurified fractions: n-hexane (HF), dichloromethane (DF), ethyl acetate (EAF), n-butanol (BF), and aqueous (AQF). BF was fractionated by reversed-phase polyamide column chromatography, obtaining 34 subfractions, which were subjected to HSCCC, where patuletin and Patulitrin were isolated. CAE and the fractions BF, EAF, DF, and AQF were analyzed by LC-DAD-MS, and patuletin and Patulitrin were determined as the major substances in EAF and BF, respectively. BF was also analyzed by HPLC and capillary electrophoresis (CE), and Patulitrin was again determined to be the main substance in this fraction. CAE and the semipurified fractions (750, 500, 300, 100, and 50 mg/L) were assayed for larvicidal activity against Aedes aegypti, with mortality rate expressed as percentage. All fractions except AQF showed insecticidal activity after 24 h exposure of larvae to the highest concentration. However, EAF showed the highest activity with more than 50% reduction in larval population at 50 mg/L.
CONCLUSIONS:
The insecticidal activity observed with EAF might have been due to the higher concentration of patuletin present in this fraction.

Nat Prod Res. 2012;26(17):1584-93.

Determination of antioxidant activity of extracts and fractions obtained from Galinsoga parviflora and Galinsoga quadriradiata, and a qualitative study of the most active fractions using TLC and HPLC methods.[Pubmed: 22085305 ]

Taking into account the role of reactive oxygen species in the development of inflammation, and the application of the plants of genus Galinsoga Ruiz & Pav. in folk medicines for inflammatory states, we investigated and compared the antioxidant activities of particular Galinsoga extracts and fractions.
METHODS AND RESULTS:
The compositions of the most active fractions were studied using thin layer chromatography (TLC) and high-performance liquid chromatography (HPLC) methods. The extracts and fractions from Galinsoga parviflora Cav. and Galinsoga quadriradiata Ruiz et Pav. possess dose-dependent free radical-scavenging ability against DPPH• and superoxide radicals, as well as inhibitory effects on linoleic acid peroxidation in a manner comparable to gallic acid. In the most active fractions, flavonoids, Patulitrin, quercimeritrin, quercitagetrin and caffeoyl derivatives were detected.
CONCLUSIONS:
Our research demonstrates that the investigated herbs are an interesting source of preparations with significant antioxidant effects. Our results justify the use of both raw materials in inflammatory diseases, among others, due to their ability to prevent free radical-induced deleterious effects.

In vivo:

Int J Inflam. 2013;2013:309493.

Effects of Flavonoids from French Marigold (Florets of Tagetes patula L.) on Acute Inflammation Model.[Pubmed: 24175111 ]

METHODS AND RESULTS:
The major components patuletin and Patulitrin were isolated from French marigold (florets of Tagetes patula). Patuletin and Patulitrin were found to inhibit acute inflammation in mice. Oral administration of patuletin and Patulitrin significantly suppressed hind-paw edema induced by carrageenin and histamine, while topical application of patuletin and Patulitrin significantly inhibited ear edema induced by 12-O-tetradecanoylphorbol-13-acetate and arachidonic acid.
CONCLUSIONS:
Thus, oral and topical administration of patuletin and Patulitrin inhibited acute inflammation in mice. These results suggest the anti-inflammatory efficacy of French marigold.

Patulitrin Description

Source:	The herbs of Tagetes erecta
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Cell Research:

Pharm Biol. 2015 May;53(5):672-81.

Cytotoxic and antioxidant properties of phenolic compounds from Tagetes patula flower.[Pubmed: 25539472 ]

Tagetes patula Linn. (Asteraceae) (French Marigold) flowers are used by local practitioners for cancer treatment; however, it lacks scientific justification. Identification of bioactive compounds in T. patula flower for cytotoxic and growth inhibition in human cancer cell lines along with its antioxidant properties using chemical and cell based systems.
METHODS AND RESULTS:
The T. patula flower methanol extract, its seven fractions, and three phenolic compounds including methyl protocatechuate (1), patuletin (2), and Patulitrin (3) were evaluated using sulforhodamine-B assay against HeLa, HT-144, NCI-H460, MCF-7, PC-3, and SF-268 human cancer cell lines. In parallel, antioxidant activity was evaluated using chemical (DPPH(·), deoxyribose, and lipid peroxidation assays) and cell-based chemiluminescence systems (human neutrophils and mice macrophages). The methanol extract and ethyl acetate insoluble fraction exhibited cytotoxic and growth inhibitory effects against HeLa in which 2 exhibited highest cell growth inhibition (GI50: 0.6 ± 0.1 µg/ml) and cytotoxicity (LC50: 2.5 ± 0.1 µg/ml). It also scavenged LOO(·) (IC50: 6.5 ± 0.7 µg/ml) and [Formula: see text] (IC50: 27.5 ± 1.3 μg/ml) in chemical systems and human neutrophils, respectively. However, 1 preferably scavenged H2O2-Cl(-) (IC50: 0.5 ± 0.01 μg/ml) in mice macrophages.
CONCLUSIONS:
Compound 2 from T. patula flower exhibited both growth inhibitory and cytotoxic properties while 1 and 3 were only growth inhibitory against HeLa. 1-3 also displayed antioxidant properties implying its probable role in growth inhibition/cytotoxic action. The present study provides scientific evidence for the use of T. patula flower in cancer treatment by traditional healer.

CAS No.	19833-25-1	Price	$398 / 5mg
Catalog No.	CFN95153	Purity	>=98%
Molecular Weight	494.4	Type of Compound	Flavonoids
Formula	C₂₂H₂₂O₁₃	Physical Description	Powder
Download	COA MSDS	Similar structural	Comparison (Web) (SDF)

Product Name	Patulitrin
CAS No.:	19833-25-1
Catalog No.:	CFN95153
Molecular Formula:	C₂₂H₂₂O₁₃
Molecular Weight:	494.4 g/mol
Purity:	>=98%
Type of Compound:	Flavonoids
Physical Desc.:	Powder
Targets:	Antifection
Source:	The herbs of Tagetes erecta
Solvent:	DMSO, Pyridine, Methanol, Ethanol, etc.
Price:	$398 / 5mg
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Flavonoids Compound Library Antifection Inhibitor Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	2.0227 mL	10.1133 mL	20.2265 mL	40.4531 mL	50.5663 mL
5 mM	0.4045 mL	2.0227 mL	4.0453 mL	8.0906 mL	10.1133 mL
10 mM	0.2023 mL	1.0113 mL	2.0227 mL	4.0453 mL	5.0566 mL
50 mM	0.0405 mL	0.2023 mL	0.4045 mL	0.8091 mL	1.0113 mL
100 mM	0.0202 mL	0.1011 mL	0.2023 mL	0.4045 mL	0.5057 mL

CFN95351	New compound 11	N/A	784.6	C₃₆H₃₂O₂₀
CFN98573	Luteolin 7,3'-di-O-glucuronide	53965-08-5	638.48	C₂₇H₂₆O₁₈
CFN91094	6-Hydroxyluteolin 7-glucoside	54300-65-1	464.38	C₂₁H₂₀O₁₂
CFN90438	Nepetin-7-glucoside	569-90-4	478.40	C₂₂H₂₂O₁₂
CFN95153	Patulitrin	19833-25-1	494.4	C₂₂H₂₂O₁₃
CFN93021	Chrysoeriol-7-O-glucoside	19993-32-9	462.4	C₂₂H₂₂O₁₁
CFN98502	Diosmetin-7-O-beta-D-glucopyranoside	20126-59-4	462.41	C₂₂H₂₂O₁₁
CFN98145	Diosmin	520-27-4	608.54	C₂₈H₃₂O₁₅
CFN93075	Neodiosmin	38665-01-9	608.54	C₂₈H₃₂O₁₅
CFN98100	Lethedoside A	221289-20-9	490.5	C₂₄H₂₆O₁₁