l-arabino

Epirubicin hydrochloride (Pharmorubicin) is an adriamycin derivative, a topoisomerase (Topo) inhibitor, and a Forkhead box protein p3 (Foxp3) inhibitor. Epirubicin hydrochloride has antitumor activity.

Oleanolic acid-3-O-α-L-arabino pyranoside is a natural product that can be used in related research in the field of life sciences. Its product number is TN8640.

L-Arabinopyranose (Pectinose) is an aldopentose, including an aldehyde (CHO) functional group.

Hederagenin 28-O-{β-D-xylopyranosyl-(1→6)-β-D-glucopyranosyl ester}3-O-{α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl} is a saponin known for its antitumor and anti-inflammatory properties [1].

4-Mmethylumbelliferyl α-L-arabinopyranoside (4-Mmethylumbelliferyl α-L-arabinopyranoside) serves as a substrate for enzymes that hydrolyze arabinose-containing substrates, such as α-L-arabinopyranoside.

Cimicidanol 3-O-alpha-L-arabinoside is a natural product of Cimicifuga, Ranunculaceae. The catalog number is T4S1672 and the CAS number is 161207-05-2. Cimicidanol 3-O-alpha-L-arabinoside can be used as a reference standard.

Ellagic acid 4-O-alpha-L-arabinofuranoside is a natural product that can be used as a reference standard. The CAS number of Ellagic acid 4-O-alpha-L-arabinofuranoside is 358617-39-7.

Apigenin 6,8-di-C-alpha-L-arabinopyranoside is a useful organic compound for research related to life sciences. The catalog number is T124311 and the CAS number is 73140-47-3.

Apigenin 6-C-alpha-L-arabinopyranosyl-8-C-beta-D-xylopyranoside is a natural product from Viola yedoensis.

Ellagic acid 4-O-α-L-arabinopyranoside, extracted from Dimocarpus longan Lour. (syn. Euphoria longan Lam.), exhibits antioxidative activity [1].

7-[α-L-Arabinopyranosyl-(1→6)-β-D-glucopyranosyloxy]cuminol, a cuminol glycoside, can be isolated from *Rhodiola rosea*^[1].

2'-Deoxy-2'-fluoro-5-ethyl-arabinouridine is a Nucleoside Derivative - Fluoro-modified nucleoside, Arabino-nucleoside, 5-Modified pyrimidine nucleoside, 2'-Modified nucleoside.

3',5'-Di-O-benzoyl-2'-deoxy-2'-fluoro-5-trifluoromethyl-arabinouridine is a Nucleoside Derivative - Fluoro-modified nucleoside, Arabino-nucleoside, 5-Modified pyrimidine nucleoside, 2'-Modified nucleoside.

4-Nitrophenyl β-L-arabinopyranoside can be utilized as a detection substrate for galactosidase.

p-Nitrophenyl α-L-arabinopyranoside is a biochemical reagent that can be hydrolyzed by recombinant BgaA (rBgaA, isolated from E. coli BL21 (DE3) strain carrying pEBGA29). It has potential applications in enzyme activity assays.

4-Nitrophenyl α-L-arabinofuranoside is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

Oleanolic acid 3-O-beta-D-glucosyl-(1->3)-alpha-L-rhamnosyl(1->2)-alpha-L-arabinoside is a natural product

Luteolin-7-O-α-L-arabinopyranosyl-(1→6)-β-D-glucopyranoside, a flavonoid, exhibits antiradical activity [1].

Myricetin 3-O-α-L-arabinopyranoside, a quercetin derivative and plant flavonoid, exhibits antioxidant, antibacterial, and antiurease properties. It inhibits A2E photooxidation-induced retinal pigment epithelium (RPE) cell death and offers protection against retinal degeneration as well as blue light (BL)-induced damage in RPE cells and mouse models [1].

Nucleoside Derivatives - 5-Modified pyrimidine nucleosides, Arabino-nucleosides

2R,3R-taxifolin-3-O-α-L-arabinopyranoside is a natural product that can be used in related research in the field of life sciences. Its product number is TN8634.

Hederagenin 3-O-(2-O-acetyl-α-L-arabinopyranoside) significantly elevated alkaline phosphatase (ALP) activity and enhanced the protein expression levels of bone sialoprotein (BSP) and osteocalcin (OC).

Apigenin-6-C-β-D-xylopyranosyl-8-C-α-L-arabinopyranoside, a flavonoid known for its antioxidant activity, can be isolated from the Traditional Chinese Medicine Tiepi Shihu [1].

3'-Deoxy-1,2-O-isopropylidene-5-O-(p-toluoyl)-L-arabinofuranose is a purine nucleoside analog that exerts antitumor activity by inhibiting DNA synthesis and inducing apoptosis, and it can target inert lymphoid malignancies.