Boc-D-Asp(OcHex)-OH is an aspartic acid derivative[1].
2,4-D sodium salt (Sodium 2,4-dichlorophenoxyacetate) is a selective systemic herbicide for the control of broad-leaved weeds. 2,4-D sodium salt acts as a plant hormone, causing uncontrolled growth in the meristematic tissues. 2,4-D sodium salt inhibits DNA and protein synthesis and thereby prevents normal plant growth and development[1].
L-Lysine ethyl ester dihydrochloride is a lysine derivative[1].
4’-Methyladenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
NHS-NH-(diethylamino)ethyl benzoate is a compound that can be used for N-glycan labeling[1].
Benalaxyl-d5is the deuterium labeledBenalaxyl(HY-121109)[1]. Benalaxyl is a fungicide, but A. fumigatus isolates are intrinsically resistant to Benalaxyl[2].
Z-β-D-HomoAla-OH is an alanine derivative[1].
(S)-3-(4-Hydroxyphenyl)-2-(methylamino)propanoic acid is a tyrosine derivative[1].
C.I. Vat Yellow 2 is an agent of yellow dye and can also be used for the paper dyeing[1].
Exaluren (ELX-02) is an synthetic eukaryotic ribosome-selective glycoside that induces read through of nonsense mutations, resulting in normally localized full-length functional proteins. Exaluren is used for the research of cystic fibrosis caused by nonsense mutations[1].
S-Hexylglutathione is an S-substituted glutathione in which the hydrogen of the thiol has been replaced by a hexyl group. S-Hexylglutathione is also an competitive inhibitor against glutathione-S-transferase. S-Hexylglutathione can be used as an affinity chromatographic ligand for glutathione-S-transferase and glutathione peroxidase[1][2].
4-Fluorobenzonitrile-d4 is the deuterium labeled 4-Fluorobenzonitrile[1].
Fmoc-D-Phe(4-I)-OH is a phenylalanine derivative[1].
Ammonium sulphate,≥99.0%,AR is an inorganic sulfate salt used for molecular biology[1].
Olivil monoacetate is found in Gymnosporia varialilis Loes[1].
Fmoc-Val-Gly-OH is a Glycine (HY-Y0966) derivative[1].
1b-Benzoyl-8a-cinnamoyl-4a,5a-dihydroxydihydroagarofuran is a sesquiterpenoid isolated from the root bark of Tripterygium hypoglaucum containing a benzoyl and a cinnamoyl group[1].
Maoecrystal B is a diterpenoids compound isolated from the leaves of Isodon eriocalyx var. laxiflora[1].
(25R)-Spirost-4-ene-3,6,12-trione is a natural product, that can be isolated from T. terrestris L[1].
2-Amino-2-(thiophen-3-yl)acetic acid is a Glycine (HY-Y0966) derivative[1].
Dihydromicromelin B is a natural product that can be isolated from the leaves of Micromelum integerrimum[1].
Benzyl alcohol-13C6 is the 13C labeled Benzyl alcohol[1].
N-Trityl-L-serine lactone is a serine derivative[1].
Protopine, an isoquinoline alkaloid contained in plants in northeast Asia.IC50 Value:Target:In vitro: Protopine was found to reduce nitric oxide (NO), cyclooxygenase-2 (COX-2), and prostaglandin E(2) (PGE(2)) production by LPS-stimulated Raw 264.7 cells, without a cytotoxic effect. Pre-treatment of Raw 264.7 cells with protopine reduced the production of pro-inflammatory cytokines [2]. Protopine is a novel microtubule stabilizer with anticancer activity in HRPC cells through apoptotic pathway by modulating Cdk1 activity and Bcl-2 family of proteins [3]. In HepG2 cells, protopine significantly increased CYP1A1 mRNA levels after 24h exposure at concentrations from 25 and 10 μM. Protopine also dose-dependently increased CYP1A1 and CYP1A2 mRNA levels in human hepatocytes [4].In vivo: Assays were performed on MDA-MB-231 human breast cancer cells, and the result showed that protopine exhibited anti-adhesive and anti-invasion effects in MDA-MB-231 cells; after treatment with protopine for 90 min, the expression of EGFR, ICAM-1, αv-integrin, β1-integrin and β5-integrin were remarkably reduced [1].
Fmoc-Ile-OH is an isoleucine derivative[1].
H-Phe(3,4-DiCl)-OH is a phenylalanine derivative[1].
5,6,7,40-Tetrahydroxyisoflavone-6,7-di-o-b-D-glucopyranoside is an isoflavonoid glycoside isolated from Pueraria lobata[1].
Timtraxanib (AVI-3207) is a selective VEGF-2 inhibitor. Timtraxanib can be used for the research of senile macular degeneration[1].
Xylotriose is a natural xylooligosaccharide, acts as a bifidogenic factor[1].
Cyanine5 amine hydrochloride is a potent fluorescent dye. Cyanine5 amine hydrochloride can be reacted with terminal alkynes via a copper-catalyzed click reaction (CuAAC). (λex=646 nm, λem=662 nm)[1].