Search Result

Results for "

Camellia sinensis

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (1) Drug Derivative (1) Drug Intermediate (1) EGFR (1) Fungal (1)
By Research Areas:	Cancer (2) Infection (2)

Inhibitors & Agonists

Natural
Products

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-N2524

Camelliaside A	EGFR	Cancer
Camelliaside A is a phytochemical and also a HER2 ligand. Camelliaside A shows no inhibitory effect on mycelial growth of Rhizoctonia solani, indicating no antifungal activity against this pathogen. Camelliaside A is applicable to breast cancer-related research .

HY-N12153

Theasaponin E2	Others	Cancer
Theasaponin E2 shows cytotoxicity against K562 and HL60 cells (IC₅₀: 14.7 μg/mL). Theasaponin E2 can be isolated from Camellia sinensis .

HY-17517

Tiadinil	Fungal Biochemical Assay Reagents	Infection
Tiadinil is a systemic acquired resistance (SAR) inducer, plant elicitor and antifungal agent. Tiadinil promotes the production of herbivore-induced plant volatiles in Camellia sinensis (tea plant). Tiadinil inhibits mycelial growth, spore germination and germ tube elongation of Stagonosporopsis citrulli in vitro. Tiadinil can be used in studies related to vine blight .

HY-W711045

Deoxygeraniol	Drug Derivative	Others
Deoxygeraniol, a monoterpenoid, has been reported in Camellia sinensis, Magnolia sieboldii, and Zingiber officinale. It is commonly used as an intermediate in the synthesis of fragrances or flavorings.

HY-N19888

β-Maltoside	Others	Others
β-Maltoside is a 2-phenylethyl glycoside. β-Maltoside resists hydrolysis by purified β-primeverosidase derived from fresh Camellia sinensis var. sinensis cv. Yabukita leaves .

HY-N17379

Camelliquercetiside D	Others	Others
Camelliquercetiside D is a natural product. Camelliquercetiside D can be isolated from the leaves of Camellia sinensis. Camelliquercetiside D inhibits alcohol dehydrogenase, with an IC₅₀ of 41.5 μM against yeast ADH. Camelliquercetiside D exhibits scavenging activity against DPPH .

HY-N17378

Camelliquercetiside B	Others	Others
Camelliquercetiside B is a natural product. Camelliquercetiside B can be isolated from the leaves of Camellia sinensis. Camelliquercetiside B inhibits alcohol dehydrogenase (Alcohol dehydrogenase), with an IC₅₀ of 13.7 μM against yeast alcohol dehydrogenase. Camelliquercetiside B exhibits scavenging activity against DPPH free radicals .

HY-W747972A

(Z)-3-Hexenal	Drug Intermediate	Infection
(Z)-3-Hexenal is an isomer of Hydrosorbaldehyde (HY-W747972). (Z)-3-Hexenal is a green leaf volatile and also the main contributor to the fresh, grassy aroma of tea leaves. (Z)-3-Hexenal undergoes irreversible conversion to (E)-2-hexenal via (Z)-3:(E)-2-hexenal isomerase (CsHI). (Z)-3-Hexenal plays a key role in protecting plants against biotic stresses (such as pathogens and insects) and acting as a signaling chemical .

Camelliaside A	Flavonols Structural Classification Flavonoids Classification of Application Fields Phenols Polyphenols Camellia sinensis (L.) O. Ktze. Plants Inflammation/Immunology Disease Research Fields Source Classification Theaceae	EGFR
Camelliaside A is a phytochemical and also a HER2 ligand. Camelliaside A shows no inhibitory effect on mycelial growth of Rhizoctonia solani, indicating no antifungal activity against this pathogen. Camelliaside A is applicable to breast cancer-related research .

Theasaponin E2	Triterpenes Structural Classification Terpenoids Camellia sinensis (L.) O. Ktze. Plants Pentacyclic Triterpenoids Source Classification Theaceae	Others
Theasaponin E2 shows cytotoxicity against K562 and HL60 cells (IC₅₀: 14.7 μg/mL). Theasaponin E2 can be isolated from Camellia sinensis .

Deoxygeraniol	Structural Classification Other Monoterpenes Terpenoids Magnoliaceae Oyama sieboldii (K. Koch) N. H. Xia & C. Y. Wu Plants Source Classification	Drug Derivative
Deoxygeraniol, a monoterpenoid, has been reported in Camellia sinensis, Magnolia sieboldii, and Zingiber officinale. It is commonly used as an intermediate in the synthesis of fragrances or flavorings.

β-Maltoside	Structural Classification Polysaccharides Camellia sinensis (L.) O. Ktze. Plants Saccharides Source Classification Theaceae	Others
β-Maltoside is a 2-phenylethyl glycoside. β-Maltoside resists hydrolysis by purified β-primeverosidase derived from fresh Camellia sinensis var. sinensis cv. Yabukita leaves .

Camelliquercetiside D	Structural Classification Flavonols Flavonoids Camellia sinensis (L.) O. Ktze. Plants Source Classification Theaceae	Others
Camelliquercetiside D is a natural product. Camelliquercetiside D can be isolated from the leaves of Camellia sinensis. Camelliquercetiside D inhibits alcohol dehydrogenase, with an IC₅₀ of 41.5 μM against yeast ADH. Camelliquercetiside D exhibits scavenging activity against DPPH .

Camelliquercetiside B	Structural Classification Flavonols Flavonoids Camellia sinensis (L.) O. Ktze. Plants Source Classification Theaceae	Others
Camelliquercetiside B is a natural product. Camelliquercetiside B can be isolated from the leaves of Camellia sinensis. Camelliquercetiside B inhibits alcohol dehydrogenase (Alcohol dehydrogenase), with an IC₅₀ of 13.7 μM against yeast alcohol dehydrogenase. Camelliquercetiside B exhibits scavenging activity against DPPH free radicals .

(Z)-3-Hexenal	Structural Classification Ketones, Aldehydes, Acids Camellia sinensis (L.) O. Ktze. Plants Source Classification Theaceae	Drug Intermediate
(Z)-3-Hexenal is an isomer of Hydrosorbaldehyde (HY-W747972). (Z)-3-Hexenal is a green leaf volatile and also the main contributor to the fresh, grassy aroma of tea leaves. (Z)-3-Hexenal undergoes irreversible conversion to (E)-2-hexenal via (Z)-3:(E)-2-hexenal isomerase (CsHI). (Z)-3-Hexenal plays a key role in protecting plants against biotic stresses (such as pathogens and insects) and acting as a signaling chemical .

Inquiry Online

Your information is safe with us. * Required Fields.

MCE Japan Authorized Agent ナミキ商事株式会社コスモ・バイオ株式会社重松貿易株式会社
Salutation			Country or Region *
Applicant Name *			Organization Name *
Department *
Email Address *			Product Name *
Cat. No.			Requested quantity *
Phone Number *
Remarks

Inquiry Online

Inquiry Information

Product Name:
Cat. No.:
Quantity:
MCE Japan Authorized Agent:

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

MedchemExpress Validation 03

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred

MedchemExpress Validation 04

MedchemExpress Validation

We use cookies

MedChemExpress values your privacy and your trust is important to us. We use cookies to enhance your website experience. Some cookies are necessary to run the website. Privacy and Cookie Policy

Name
Email *

	Sorry, but the email address you supplied was invalid.

Camellia sinensis

Inhibitors & Agonists

NaturalProducts

Natural
Products