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巴豆属

巴豆属

Cat. No. Product Name CAS No. Purity Chemical Structure
TN2974 3-O-Methylquercetin tetraacetate
化合物 TN2974
1486-69-7 98%
Quercetin 3-O-methyl ether is a potent phosphodiesterase (PDE)3/4 inhibitor, it has potential for treating asthma against ovalbumin-induced airway hyperresponsiv...
TN3945 Ent-3-Oxokauran-17-oic acid
化合物 TN3945
151561-88-5 98%
ent-3-Oxokauran-17-oic acid 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3945,CAS号为 151561-88-5。
TN4392 Koaburaside
化合物 TN4392
41653-73-0 98%
Koaburaside exhibits antioxidant activity with an IC50 value of 9.0μM, it shows weak inhibitory activity against influenza A neuraminidase. Koaburaside may have ...
TN4393 Koaburaside monomethyl ether
化合物 TN4393
41514-64-1 98%
Koaburaside monomethyl ether是一种天然产物,属于大戟科巴豆属,其产品编号为 TN4393,CAS号为 41514-64-1。Koaburaside monomethyl ether可用作对照参考。
T5136 Kongensin A
化合物 T5136
885315-96-8 98%
Kongensin A is an effective heat shock protein 90 (HSP90) inhibitor that has potential anti-necroptosis and anti-inflammation applications.
TN3943 Ent-17-Hydroxykauran-3-one
化合物 TN3943
960589-81-5 98%
ent-17-Hydroxy-16α-kauran-3-one shows weak antimicrobial activity when tested against Staphylococcusaureus.
TN3946 Ent-3-Oxokaurane-16,17-diol
化合物 TN3946
135683-73-7 98%
AKaurane-3,16,17-triol,ent-kaurane-3-oxo-16α,17-diol,and ent-16α,17-dihydroxyatisan-3-one are three kinds of toxic diterpenoids isolated from the roots of genus ...
TN3959 Ent-kaurane-3,16,17-triol
化合物 TN3959
130855-22-0 98%
Kaurane-3,16,17-triol,ent-kaurane-3-oxo-16α,17-diol,and ent-16α,17-dihydroxyatisan- 3-one are three kinds of toxic diterpenoids isolated from the roots of genus ...
TN1266 3-O-Methylquercetin
3-邻甲基槲皮素
1486-70-0 99.8%
3-O-Methylquercetin 是分离自植物Rhamnus nakaharai 的天然产物,可抑制总 cAMP 和cGMP-phosphodiesterase (PDE)。它对PDE1、PDE5、PDE 和PDE4的IC50分别是31.9 μM、86.9 μM、18.6 μM 和1.6 μM。
T3929 Kaurenoic acid
异贝壳杉烯酸
6730-83-2 99.7%
Kaurenoic acid (kaurenoate) 是一种二萜,来源于 Sphagneticola trilobata 中,可以抑制细胞因子的产生和激活 NO–cyclic GMP–PKG–ATP- 敏感型钾通道信号通路,并抑制炎症疼痛。
TN1643 Ferulamide
阿魏酸酰胺
61012-31-5 99.45%
Ferulamide (4-Hydroxy-3-methoxycinnamide) 是从巴豆中分离的阿魏酸衍生物,具有抗胆碱酯酶活性。
T6S0033 Crotonoside
巴豆苷
1818-71-9 98%
Crotonoside (Isoguanosine) 是从中草药巴豆中分离出来的一种天然产物。 它抑制 FLT3 和 HDAC3/6,有治疗急性髓性白血病 (AML)的研究潜力。
3-O-Methylquercetin tetraacetate
TN2974
Quercetin 3-O-methyl ether is a potent phosphodiesterase (PDE)3/4 inhibitor, it has potential for treating asthma against ovalbumin-induced airway hyperresponsiv...
ent-3-Oxokauran-17-oic acid
TN3945
ent-3-Oxokauran-17-oic acid 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3945,CAS号为 151561-88-5。
Koaburaside
TN4392
Koaburaside exhibits antioxidant activity with an IC50 value of 9.0μM, it shows weak inhibitory activity against influenza A neuraminidase. Koaburaside may have ...
Koaburaside monomethyl ether
TN4393
Koaburaside monomethyl ether是一种天然产物,属于大戟科巴豆属,其产品编号为 TN4393,CAS号为 41514-64-1。Koaburaside monomethyl ether可用作对照参考。
Kongensin A
T5136
Kongensin A is an effective heat shock protein 90 (HSP90) inhibitor that has potential anti-necroptosis and anti-inflammation applications.
ent-17-Hydroxykauran-3-one
TN3943
ent-17-Hydroxy-16α-kauran-3-one shows weak antimicrobial activity when tested against Staphylococcusaureus.
ent-3-Oxokaurane-16,17-diol
TN3946
AKaurane-3,16,17-triol,ent-kaurane-3-oxo-16α,17-diol,and ent-16α,17-dihydroxyatisan-3-one are three kinds of toxic diterpenoids isolated from the roots of genus ...
ent-kaurane-3,16,17-triol
TN3959
Kaurane-3,16,17-triol,ent-kaurane-3-oxo-16α,17-diol,and ent-16α,17-dihydroxyatisan- 3-one are three kinds of toxic diterpenoids isolated from the roots of genus ...
3-O-Methylquercetin
TN1266
3-O-Methylquercetin 是分离自植物Rhamnus nakaharai 的天然产物,可抑制总 cAMP 和cGMP-phosphodiesterase (PDE)。它对PDE1、PDE5、PDE 和PDE4的IC50分别是31.9 μM、86.9 μM、18.6 μM 和1.6 μM。
Kaurenoic acid
T3929
Kaurenoic acid (kaurenoate) 是一种二萜,来源于 Sphagneticola trilobata 中,可以抑制细胞因子的产生和激活 NO–cyclic GMP–PKG–ATP- 敏感型钾通道信号通路,并抑制炎症疼痛。
Ferulamide
TN1643
Ferulamide (4-Hydroxy-3-methoxycinnamide) 是从巴豆中分离的阿魏酸衍生物,具有抗胆碱酯酶活性。
Crotonoside
T6S0033
Crotonoside (Isoguanosine) 是从中草药巴豆中分离出来的一种天然产物。 它抑制 FLT3 和 HDAC3/6,有治疗急性髓性白血病 (AML)的研究潜力。
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