AdooQ BioScience is a supplier of biochemicals located in Irvine, CA since 2006. In the past five years, we have been a renowned name engaged in manufacturing and supplying small molecule inhibitors including kinase inhibitors on kinds of signal pathway, such as PI3K, AKT, HDAC, MARP etc.
Company WebsiteSchisanhenol is a valuable natural product worthy to be investigated as a potential.
More Information Supplier PageSchisanhenol is a valuable natural product worthy to be investigated as a potential.
More Information Supplier PageSchisanhenol is a valuable natural product worthy to be investigated as a potential.
More Information Supplier PageSchisantherin A is a dibenzocyclooctadiene that exhibits anti-tussive, sedative, anti-inflammatory, anti-osteoporotic, neuroprotective, cognition enhancing, and cardioprotective activities. In macrophages, Gomisin C decreases LPS-induced expression and activity of iNOS, COX-2, NO, IL-6, and TNF-??.
More Information Supplier PageSchisantherin A is a dibenzocyclooctadiene that exhibits anti-tussive, sedative, anti-inflammatory, anti-osteoporotic, neuroprotective, cognition enhancing, and cardioprotective activities. In macrophages, Gomisin C decreases LPS-induced expression and activity of iNOS, COX-2, NO, IL-6, and TNF-??.
More Information Supplier PageSchisantherin A is a dibenzocyclooctadiene that exhibits anti-tussive, sedative, anti-inflammatory, anti-osteoporotic, neuroprotective, cognition enhancing, and cardioprotective activities. In macrophages, Gomisin C decreases LPS-induced expression and activity of iNOS, COX-2, NO, IL-6, and TNF-??.
More Information Supplier PageSchisantherin B, extracted from Schisandra chinensis (Turcz.)Baill. seeds and stems.
More Information Supplier PageSchisantherin B, extracted from Schisandra chinensis (Turcz.)Baill. seeds and stems.
More Information Supplier PageSchisantherin B, extracted from Schisandra chinensis (Turcz.)Baill. seeds and stems.
More Information Supplier PageSclareol is a fragrant chemical compound found in clary sage (Salvia sclarea), from which it derives its name. It is classified as a bicyclic diterpene alcohol. Sclareol is used as a fragrance in cosmetics and perfumes and as flavoring in food. Sclareol and other similar substances may be prepared from sclareolide.Sclareol is also able to […]
More Information Supplier PageSclareol is a fragrant chemical compound found in clary sage (Salvia sclarea), from which it derives its name. It is classified as a bicyclic diterpene alcohol. Sclareol is used as a fragrance in cosmetics and perfumes and as flavoring in food. Sclareol and other similar substances may be prepared from sclareolide.Sclareol is also able to […]
More Information Supplier PageSclareolide (Norambreinolide) is a sesquiterpene lactone natural product .
More Information Supplier PageSclareolide (Norambreinolide) is a sesquiterpene lactone natural product .
More Information Supplier PageScoparone is a compound found in the herb, Yin Chin, that can up-regulate the expression and activate the CAR (constitutive androstane receptor) found in the liver.
More Information Supplier PageScoparone is a compound found in the herb, Yin Chin, that can up-regulate the expression and activate the CAR (constitutive androstane receptor) found in the liver.
More Information Supplier PageScoparone is a compound found in the herb, Yin Chin, that can up-regulate the expression and activate the CAR (constitutive androstane receptor) found in the liver.
More Information Supplier PageSCR7 is a specific DNA Ligase IV inhibitor. SCR7 inhibits end joining of double strand breaks in diverse cell types resulting in tumour regression by activation of p53 mediated apoptosis.
More Information Supplier PageSCR7 is a specific DNA Ligase IV inhibitor. SCR7 inhibits end joining of double strand breaks in diverse cell types resulting in tumour regression by activation of p53 mediated apoptosis.
More Information Supplier PageSCR7 is a specific DNA Ligase IV inhibitor. SCR7 inhibits end joining of double strand breaks in diverse cell types resulting in tumour regression by activation of p53 mediated apoptosis.
More Information Supplier PageScrambled 10Panx, Panx-1 mimetic inhibitory peptide, is a blocker of pannexin-1 gap junctions.
More Information Supplier PageScrambled 10Panx, Panx-1 mimetic inhibitory peptide, is a blocker of pannexin-1 gap junctions.
More Information Supplier PageScrambled 10Panx, Panx-1 mimetic inhibitory peptide, is a blocker of pannexin-1 gap junctions.
More Information Supplier PageScutellarin is a flavonoid that exhibits a number of cardio- and neuro-protective effects.
More Information Supplier PageScutellarin is a flavonoid that exhibits a number of cardio- and neuro-protective effects.
More Information Supplier PageScutellarin is a flavonoid that exhibits a number of cardio- and neuro-protective effects.
More Information Supplier PageSD 1008 is reported to be a JAK2/STAT3 signaling pathway inhibitor which additionally inhibits Src. SD 1008 is noted to induce apoptosis in cell lines that express constitutively active tyrosine-phosphorylated STAT3.
More Information Supplier PageSD 1008 is reported to be a JAK2/STAT3 signaling pathway inhibitor which additionally inhibits Src. SD 1008 is noted to induce apoptosis in cell lines that express constitutively active tyrosine-phosphorylated STAT3.
More Information Supplier PageSDZ 205-557 is a potent, selective 5-HT4 serotonin receptor antagonist.
More Information Supplier PageSDZ 205-557 is a potent, selective 5-HT4 serotonin receptor antagonist.
More Information Supplier PageSDZ 205-557 is a potent, selective 5-HT4 serotonin receptor antagonist.
More Information Supplier PageSDZ 220-581 ammonium salt is a potent, competitive antagonist at the NMDA glutamate receptor subtype(pKi= 7.7).
More Information Supplier PageSDZ 220-581 ammonium salt is a potent, competitive antagonist at the NMDA glutamate receptor subtype(pKi= 7.7).
More Information Supplier PageSDZ 220-581 ammonium salt is a potent, competitive antagonist at the NMDA glutamate receptor subtype(pKi= 7.7).
More Information Supplier PageSEA0400 is a novel and selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
More Information Supplier PageSEA0400 is a novel and selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
More Information Supplier PageSEA0400 is a novel and selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
More Information Supplier PageSec-O-glucosylhamaudol is one of the major bioactive compounds of the Saposhnikoviae Radix.
More Information Supplier PageSec-O-glucosylhamaudol is one of the major bioactive compounds of the Saposhnikoviae Radix.
More Information Supplier PageSec-O-glucosylhamaudol is one of the major bioactive compounds of the Saposhnikoviae Radix.
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