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- Acanthaceae Extract
Acanthaceae Extract
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- Simsia foetida (Cav.) S.F.Blake (42)
- Conioselinum smithii (H. Wolff) Pimenov & Kljuykov (28)
- Alfredia cernua (L.) Cass. (8)
- Senecio latifolius DC. (6)
- Jacobaea cannabifolia (Less.) E. Wiebe (5)
- Acmella paniculata (Wall. ex DC.) R. K. Jansen (4)
- Cremanthodium helianthus (Franch.) W. W. Sm. (4)
- Vernonia adoensis (4)
- Arnica chamissonis Less. (3)
- Picris rhagadioloides (L.) Desf. (3)
- Rhaponticum chinense (S. Moore) L. Martins & Hidalgo (3)
- Senecio polypodioides Greene (3)
- Ambrosia artemisiifolia L. (2)
- Blepharis ciliaris (L.) B.L.Burtt (2)
- Cirsium vulgare(Savi) Ten. (2)
- Elsholtzia kachinensis Prain (2)
- Hypoestes purpurea (L.) R. Br. (2)
- Jacobaea maritima (L.) Pelser & Meijden (2)
- Justicia adhatodaL. (2)
- Lepidagathis cuspidata Nees (2)
- Petasites tatewakianus Kitam. (2)
- Psiadia argutaVoigt (2)
- Taraxacum obovatum (Willd.) DC. (2)
- Blepharis edulis (Forssk.) Pers. (1)
- Isodon albopilosus (C. Y. Wu & H. W. Li) H. Hara (1)
- Justicia gendarussa N. L. Burman (1)
- Salvia argentea L. (1)
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Acanthaceae Extract (103)
- Formula: C36H40O19
- Molecular Weight: 776.70
Ciliatoside A is a naturally bioactive compound that exhibits significant anti-inflammatory, antiviral, and neuroprotective activities. Ciliatoside A serves as a mitophagy inducer and NLRP3 inflammasome inhibitor, activating AMPK, SIRT1, and the PINK1/Parkin axis, and inhibiting pyroptosis and apoptosis. Ciliatoside A promotes autophagic flux, autophagosome-lysosome fusion, mTOR inhibition, and p62-dependent HBc degradation; reduces Aβ aggregation, plaque deposition, microglial/astrocyte activation, and bacterial load; and maintains neuronal integrity, mitochondrial membrane potential, and ATP production. Ciliatoside A is used in research on Alzheimer's disease, Klebsiella pneumoniae-induced pneumonia, hepatitis B virus infection, and inflammation.
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- Formula: C22H20O7
- Molecular Weight: 396.40
Pronaphthalide A is a cytotoxic agent and an inhibitor of SFTSV glycoprotein Gn (domain B) (Kd = 0.74 mM). It blocks viral binding and internalization by binding to the conserved B domain of SFTSV Gn, thereby inhibiting SFTSV infection at the viral entry stage, and exhibits broad-spectrum antiviral activity against bunyaviruses. Pronaphthalide A can be used for research on gastric cancer, severe fever with thrombocytopenia syndrome, and HIV/AIDS.
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- Formula: C26H26O12
- Molecular Weight: 530.48
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- Formula: C36H40O19
- Molecular Weight: 776.70
Procumbenoside E is an arylnaphthalene lignan glycoside compound discovered from Justicia procumbens, and it possesses an arylnaphthalene lignan skeleton and a diphyllin structure.
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- Formula: C41H48O23
- Molecular Weight: 908.81
Procumbenoside F is a lignan glycoside compound that can be isolated and extracted from Justicia procumbens L.. Procumbenoside F can be used in cancer research.
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- Formula: C31H32O15
- Molecular Weight: 644.58
Procumbenoside A is a lignan glycoside discovered in Justicia procumbens. Procumbenoside A inhibits HIV-1 replication with an IC50 of 4.95 μM. Procumbenoside A exerts cytotoxic effects on various cancer cells. Procumbenoside A induces Cu (II)-mediated strand breaks in supercoiled plasmid DNA, generating the relaxed circular DNA form, while no linear form is detected. Procumbenoside A is used in studies related to liver cancer, colon adenocarcinoma, and HIV-1 infection.
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- Formula: C27H36O9
- Molecular Weight: 504.58
8,8'-Lignan-3,3',4,4',5,9,9'-heptol is a dibenzylbutane-type lignan that can be found in Justicia procumbens. It is useful for research related to lignan components and natural product chemistry.
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- Formula: C26H24O12
- Molecular Weight: 528.47
Justalakonin is an arylnaphthalene glycoside that is found in Justicia purpurea. Justalakonin exhibits no significant inhibitory effects on lipid peroxidation, COX‑1, or the proliferation of various tumor cells, but possesses COX-2 inhibitory activity.
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- Formula: C20H29NaO7S
- Molecular Weight: 436.49
Sodium 14-deoxy-8,9-didehydro andrographolide-12(R)-sulfonate is a natural product that can be found in Andrographis paniculata.
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- Formula: C20H36O7P2
- Molecular Weight: 450.45
ent-Copalyl diphosphate (ent-CPP) is a terpenoid precursor and metabolite involved in plant biosynthetic pathways. ent-Copalyl diphosphate participates in metabolism of natural products including phytoalexins in rice and maize, and steviol glycoside in Stevia rebaudiana.
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- Formula: C46H74O16
- Molecular Weight: 883.07
Clemontanoside-C is an oleanane-based triterpenoid saponin and antifungal agent found in the roots of Lepidagathis cuspidata. Clemontanoside-C acts against Aspergillus flavus, Rhizopus stolinifer, Penicillum nodatum, and Aspergillus fumigatus. Clemontanoside-C can be used for the research of fungal infections.
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- Formula: C21H32O5
- Molecular Weight: 364.48
14-Deoxy-12-methoxyandrographolide, an ent-labdane-type diterpenoid found in the aerial parts of Andrographis paniculata, is a cell differentiation inducer. 14-Deoxy-12-methoxyandrographolide induces differentiation of myeloid leukemia cells via increased phagocytosis of polystyrene latex particles. 14-Deoxy-12-methoxyandrographolide can be used for the research of myeloid leukemia.
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- Formula: C21H14O7
- Molecular Weight: 378.33
Justicidin F (Taiwanin E methyl ether) is a lignan found in Justicia procumbens Linn. var. leucantha Honda.
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- Formula: C30H28O12
- Molecular Weight: 580.54
Naringenin-7-O-(6′′-E-p-coumaroyl-β-D-glucopyranoside) (Compound 6) is a natural product. Naringenin-7-O-(6′′-E-p-coumaroyl-β-D-glucopyranoside) can be isolated from the aerial parts of Blepharis ciliaris (L.) B.L. Burtt. Naringenin-7-O-(6′′-E-p-coumaroyl-β-D-glucopyranoside) does not exhibit antioxidant activity.
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- Formula: C28H36O14
- Molecular Weight: 596.58
Magnolenin C is a glycoside with a ketolignan structure. Magnolenin C can be isolated from the aerial parts of Acanthus ebracteatus.
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- Formula: C20H30O3
- Molecular Weight: 318.45
8-Methylandrograpanin (Compound I) is a diterpene found in the leaves of Andrographis paniculata (Burm.f.) Nees.
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- Formula: C24H26O11
- Molecular Weight: 490.46
Andrographidine E is a COX-2 (IC50 = 19 μM) and HDAC inhibitor, with high affinity for HDAC1 and HDAC3. Andrographidine E can specifically bind to macrophages and has potential immunotargeting properties. Andrographidine E can be used for studying inflammation.
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