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Results for "

japonicus

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    28
    TargetMol | Inhibitors_Agonists
  • Dye Reagents
    1
    TargetMol | Dye_Reagents
  • Natural Products
    27
    TargetMol | Natural_Products
  • Recombinant Protein
    1
    TargetMol | Recombinant_Protein
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    1
    TargetMol | Inhibitors_Agonists
Ophiogenin 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside
Ophiogenin-3-O-alpha-L-rhaMnopyranosyl-(1->2)-beta-D-glucopyranoside
T3S1250128502-94-3
Ophiogenin 3-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside (Ophiogenin-3-O-alpha-L-rhaMnopyranosyl-(1->2)-beta-D-glucopyranoside) is a natural product with significant pharmacological effects on the cardiovascular system.
  • $152
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Petasites japonicus extract
TN841491845-41-9
Petasites japonicus extract, derived from Petasites japonicus, possesses antioxidant, anti-inflammatory, anti-obesity, neuroprotective, and anticancer properties. It promotes osteoblast differentiation by upregulating Runx2 and Osterix in MC3T3-E1 cells.
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Ophiopogonin C
Ophiopogonin C
T1380565586-25-6
Ophiopogonin C is a natural product isolated from the tubers of Ophiopogon japonicus, is a rare naturally occurring C29 steroidal glycoside.
  • $253
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TargetMol | Citations Cited
Leukotriene B4
5(S),12(R)-DiHETE
T1404571160-24-2
Leukotriene B4 (LTB4) is a compound derived from arachidonic acid via the 5-lipoxygenase pathway that mediates certain inflammatory and immune responses. Leukotriene B4 induces neutrophil extracellular traps that impede the clearance of Pneumocystis japonicus.
  • $722
35 days
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(rel)-Asperparaline A
T37609195966-93-9
Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces T. colubriformis fecal egg count in gerbils.3References1. Hayashi, H., Nishimoto, Y., Akiyama, K., et al. New paralytic alkaloids, asperparalines A, B and C, from Aspergillus japonicus JV-23. Biosci. Biotechnol. Biochem. 64(1), 111-115 (2000).2. Hirata, K., Kataoka, S., Furutani, S., et al. A fungal metabolite asperparaline a strongly and selectively blocks insect nicotinic acetylcholine receptors: The first report on the mode of action. PLoS One 6(4), e18354 (2011).3. Banks, R.M., Blanchflower, S.E., Everett, J.R., et al. Novel anthelmintic metabolites from an Aspergillus species; the aspergillimides. J. Antibiot. (Tokyo) 50(10), 840-846 (1997). Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces T. colubriformis fecal egg count in gerbils.3 References1. Hayashi, H., Nishimoto, Y., Akiyama, K., et al. New paralytic alkaloids, asperparalines A, B and C, from Aspergillus japonicus JV-23. Biosci. Biotechnol. Biochem. 64(1), 111-115 (2000).2. Hirata, K., Kataoka, S., Furutani, S., et al. A fungal metabolite asperparaline a strongly and selectively blocks insect nicotinic acetylcholine receptors: The first report on the mode of action. PLoS One 6(4), e18354 (2011).3. Banks, R.M., Blanchflower, S.E., Everett, J.R., et al. Novel anthelmintic metabolites from an Aspergillus species; the aspergillimides. J. Antibiot. (Tokyo) 50(10), 840-846 (1997).
  • $265
35 days
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Raddeanin A
Raddeanin R3, NSC382873, Anemodeanin A
T387889412-79-3
Raddeanin A is a natural triterpenoid saponin from Cyperus japonicus that inhibits histone deacetylase and is also a potent immunogenic cell death inducer with strong anti-angiogenic and anti-tumor activities.
  • $40
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TargetMol | Citations Cited
Cixiophiopogon A
T3S1253288143-27-1
Cixiophiopogon A is a natural product from Ophiopogon japonicus.
  • $696
7-10 days
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14-Hydroxy sprengerinin C
T4S12471111088-89-1
14-Hydroxy sprengerinin C, a natural product derived from Ophiopogon japonicus.
  • $61
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Shizukaol G
T81166165171-11-9
Shizukaol G, a dimeric sesquiterpene, can be isolated from the roots of Chloranthus japonicus [1].
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Shizukanolide
T8116770578-36-8
Shizukanolide, a sesquiterpene lactone extracted from Chloranthus japonicus (Chloranthaceae), has a dehydro derivative that exhibits moderate antifungal activity [1].
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Preleoheterin
T81408151178-05-1
Preleoheterin (Compound 3), a labdane diterpene isolated from L. japonicus [1], exhibits anti-inflammatory properties by inhibiting the production of nitric oxide and pro-inflammatory cytokines in LPS-activated macrophages without inducing cytotoxicity at certain concentrations [2].
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Ophiopogonone C
T81601477336-77-9
Ophiopogonone C (compound 3), an isoflavone, has been isolated from the ethanol extract of the tubers of Ophiopogon japonicus [1].
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Ejaponine A
T824871253119-28-6
Ejaponine A (Compound 1), an insecticidal sesquiterpene ester derived from Euonymus japonicus, exhibits potent activity against Mythimna separata, with an LD50 of 89.2 μg/g. It is employed for the control of this pest species [1].
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6-Formyl-isoophiopogonanone B
T8326688700-30-5
6-Formyl-isoophiopogonanone B, a homoisoflavonoid, can be isolated from the species Ophiopogon japonicus [1].
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6-Aldehydoisoophiopogonone B
T83271112500-89-7
Compound 24, also known as 6-Aldehydoisoophiopogonone B, is a homoisoflavonoid extractable from Ophiopogon japonicus [1].
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(25R)-Ruscogenin-3-yl α-L-rhamnopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→4)]-β-D-glucopyranoside
T835681220707-31-2
Compound 1, (25R)-Ruscogenin-3-yl α-L-rhamnopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→4)]-β-D-glucopyranoside, is a steroidal saponin that can be isolated from the roots of Ophiopogon japonicus [1].
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Calenduloside E
Silphioside F
TJS092826020-14-4
Calenduloside E (Silphioside F) is a pentacyclic triterpene saponin extracted from Panax japonicus. It targets heat shock protein 90 (Hsp90) and has anti-apoptotic effect.
  • $117
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TargetMol | Citations Cited
6-Formyl-isoophiopogonanone A
6-Aldehydoisoophiopogonanone A
TN1304116291-82-8
6-Aldehydoisoophiopogonanone A is a natural product from Ophiopogon japonicus.
  • $197
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Isoleojaponin
TN43061840966-49-5
Isoleojaponin is a natural product from Leonurus japonicus.
  • $750
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Nodosin
TN466110391-09-0
Nodosin has anti-inflammatory function of Nodosin via inhibition of IL-2. Nodosin perfusion provides a potential protective effect through inducing HO-1 expression to attenuate ischemia reperfusion injury in liver transplantation.
  • $98
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Shizukaol A
TN5010131984-98-0
Shizukaol A is a natural product from Chloranthus japonicus.
  • $740
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3,4-Dihydroxyallylbenzene 3,4-di-O-glucoside
1,2-Di-O-β-D-glucopyranosyl-4-allylbenzene
TN6231454473-97-3
3,4-Dihydroxyallylbenzene 3,4-di-O-glucoside (1,2-Di-O-β-D-glucopyranosyl-4-allylbenzene) is a natural product found in the tuber of Ophiopogon japonicus Ker-Gawl.
  • $1,580
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Ginsenoside Rs2
TN711087733-66-2
Ginsenoside Rs2 is a natural product isolated from the leaves of Panax japonicus var..
  • $307
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11-oxo-alpha-amyrin
Neoilexonol
TN72282118-90-3
11-oxo-alpha-amyrin (Neoilexonol) is a triterpene compound extracted from Leonurus japonicus (Lamiaceae) and is a natural compound .
  • $195
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