Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN260227 Agrochelin 247115-74-8
Agrochelin, an alkaloid cytotoxicantibiotic, is produced by the fermentation of a marineAgrobacteriumsp. Agrochelin has cytotoxic activity in tumor cell lines.
YN330255 Desethyl chloroquine diphosph... 247912-76-1
Desethyl chloroquine diphosphate is a major desethyl metabolite of Chloroquine. Chloroquine diphosphate is an inhibitor ofautophagy and toll-like receptors (TLRs). Desethyl chloroquine diphosphate possesses antiplasmodic activity.
YN250787 Galidesivir 249503-25-1
Galidesivir (BCX4430), an adenosine analog and a direct-acting antiviral agent, disrupts viralRNA-dependent RNA polymerase (RdRp)activity. Galidesivir is active in vitro against many RNA viral pathogens, including the filo...
YN250045 Antibiotic-5d 251349-54-9
Antibiotic-5d is a synthesis and antimicrobial compound.
YN251818 Apelin-36(human) 252642-12-9
Apelin-36(human) is an endogenous orphan G protein-coupled receptorAPJagonist, with an EC50 of 20nM. Apelin-36(human) shows high affinity to human APJ receptors expressed in HEK 293 cells (pIC50=8.61). Apelin-36 has been l...
YN350118 5Z-7-Oxozeaenol 253863-19-3
5Z-7-Oxozeaenol is a natural anti-protozoan compound from fungal origin, acting as a potent irreversible and selective inhibitor ofTAK1 and VEGF-R2, with IC50s of 8nM and 52nM, respectively.
YN250364 Alisporivir 254435-95-5
Alisporivir (Debio-025) is acyclophilininhibitor molecule with potent anti-hepatitis C virus (HCV) activity.
YN250099 Emricasan 254750-02-2
Emricasan is a potent irreversible pan-caspase inhibitor.
YN251794 Kushenol W 254886-76-5
Kushenol W is a prenylated flavonoid that can be isolated from the root ofSophora flavescens. Kushenol W has antimicrobial effect, with a MIC of 10 μg/mL forStaphylococcus aureus.
YN250806 Artemisone 255730-18-8
Artemisone (Artemifone) is a potent and semi-syntheticantimalarial, inhibitsP. falciparumstrains, with a mean IC50 of 0.83nM. Artemisone is also a potent inhibitor ofhuman CMV.
YN371329 17-GMB-APA-GA 256337-10-7
17-GMB-APA-GA is anADC Cytotoxin. 17-GMB-APA-GA is a potent HSP90 inhibitor and used for latent T. gondii infection research.
YN250595 Favipiravir 259793-96-9
Favipiravir (T-705) is a potent and selective RNA-dependent RNA polymerase inhibitor, used to treat influenza virus infections.
YN483416 Rabdosiin 263397-69-9
Rabdosiin is a tetramer of caffeic acid isolated from the stem ofRabdosia japonicaHara. Rabdosiin possess anti-allergic activity, anti-HIV activity and inhibition on DNA topoisomerase.
YN250852 Etravirine 269055-15-4
Etravirine (TMC125) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used for the treatment of HIV.
YN250893 Pristinamycin 270076-60-3
Pristinamycin, produced byStreptomyces pristinaespiralis, is an orally active streptogramin-like antibiotic consisting of two chemically unrelated components: Pristinamycin I (PI) and Pristinamycin II (PII). Pristinamycin is ...
YN251831 PA (224-233), Influenza 271573-27-4
PA (224-233), Influenza is a 10-aa peptide, a fragment of polymerase 2 protein in influenza A virus.
YN250739 (S,S)-Valifenalate 283159-94-4
(S,S)-Valifenalate ((S,S)-IR5885) is an acylamino acidfungicide and is used to control a wide range of fungi belonging to the class of Oomycetes. (S,S)-Valifenalate ((S,S)-IR5885) interferes with the cell-wall synthesis thus...
DPC-681 is a potent and selective inhibitor of HIV protease with IC90s for wild-type HIV-1 of 4 to 40nM.
Leu-AMS (compound 6), a leucine analogue, is a potent inhibitor ofleucyl-tRNA synthetase(LRS) with an IC50 of 22.34nM, which inhibits the catalytic activity of LRS but did not affect the leucine-induced mTORC1 activation...
YN482606 Cimiracemoside D 290821-39-5
Cimiracemoside D is a natural product found in Actaea racemosa with unknown details.
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