Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN250474 Neoabietic acid 471-77-2
Neoabietic acid is an abietic-type acid isolated from the oleoresin and rosin ofPinus palustris. Neoabietic acid is highly susceptible to mineral acid. Neoabietic acid has antibacterial activity in vitro .
Pinocembrin is a major flavonoid molecule incorporated as multifunctional in the pharmaceutical industry. Its vast range of pharmacological activities has been well researched including antimicrobial, anti-inflammatory, antioxidant, and a...
YN251899 Phloracetophenone 480-66-0
Phloracetophenone (2,4,6-trihydroxyacetophenone) is the aglycone part of acetophenone glycoside obtained fromCurcuma comosaRoxb, with cholesterol-lowering activity. Phloracetophenone enhances cholesterol 7α-hydroxylase (CYP7A1) act...
YN251461 Isoimperatorin 482-45-1
Isoimperatorin, a natural furanocoumarin that can be isolated from a variety of plant parts, has analgesic, antimicrobial, vascular relaxing and anticancer activities.
Thermopsine is a quinolizidine alkaloid isolated from the fruits and pods and stem bark ofSophora velutinasubsp. Thermopsine hasantibacterialactivity.
Gossypetin is a hexahydroxylated flavonoid and is a potentmitogen-activated protein kinase kinase (MKK)3 and MKK6inhibitor with strongly attenuates theMKK3/6-p38signaling pathway, has various pharmacological activities, includin...
YN250271 Griseoluteic acid 489-76-9
Griseoluteic acid, a phenazine antibiotic, is originally isolated fromS. griseoluteus. Griseoluteic acid is a breakdown product of griseolutein A and B.
YN251941 4(3H)-Quinazolinone 491-36-1
Some 4-quinazolinone derivatives have antiplatelet activity.
kaempferide, a natural compound derived from the roots of kaempferia galanga, has a variety of effects including anti-carcinogenic, anti-inflammatory, anti-oxidant, anti-bacterial and anti-viral properties.
YN251589 Rhapontigenin 500-65-2
In vitro inhibitory concentration against proliferation of HL60 cells
YN251920 3-Nitropropanoic acid 504-88-1
3-Nitropropionic acid (3-NP) is an irreversible inhibitor of mitochondrial respiratory Complex II succinate dehydrogenase, resulting in energy depletion through disruption of the electron transport chain.
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