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T36621Prostaglandin F2β；Prostaglandin F2βProstaglandin F2β
Prostaglandin F2β (PGF2β) is the 9β-hydroxy stereoisomer of PGF2α. It is much less active than PGF2α in antifertility and bronchoconstrictor activities. PGF2β exhibits bronchodilating activity in guinea pigs and cats and antagonizes the bronchoconstrictor activity of PGF2α.
价 格：￥电议型 号：T36621产 地：中国大陆
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T362191a,1b-dihomo Prostaglandin E1；1a,1b-dihomo Prostaglandin E11a,1b-dihomo Prostaglandin E1；1a,1b-dihom
1a,1b-dihomo Prostaglandin E1 is a class of prostaglandin compounds.
价 格：￥电议型 号：T36219产 地：中国大陆
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T3621819R(20S)-EpDPA；19R(20S)-EpDPA19R(20S)-EpDPA
19R(20S)-EpDPA is an oxylipin and a metabolite of docosahexaenoic acid .1,2It is formed from DHA by various cytochrome P450 (CYP) isoforms in a stereoselective manner.219R(20S)-EpDPA (30 nM) prevents calcium-induced increases in the spontaneous beating of isolated neonatal rat cardiomyocytes (NRCMs).3
价 格：￥电议型 号：T36218产 地：中国大陆
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T3621719-hydroxy Cholesterol；19-hydroxy Cholesterol19-hydroxy Cholesterol
19-hydroxy Cholesterol is formed during metabolic oxidation of cholesterol. It has been used as an internal standard for the quantitative determination of sterols by mass spectroscopic analysis.[1]
价 格：￥电议型 号：T36217产 地：中国大陆
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T3621517R(18S)-EpETE；17R(18S)-EpETE17R(18S)-EpETE
17R(18S)-EpETE is an oxylipin and a cytochrome P450 metabolite of eicosapentaenoic acid .1,217R(18S)-EpETE is an activator of large-conductance calcium-activated potassium (BKCa) channels, increasing the potassium current amplitude by 15-fold in isolated rat cerebral artery vascular smooth muscle cells (VSMCs) at +60 mV when used at a concentration of 50 nM.2It has negative chronotropic effects in isolated neonatal rat cardiomyocytes (NRCMs; EC50= ~1-2 nM) and prevents calcium-induced increases
价 格：￥电议型 号：T36215产 地：中国大陆
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T3621416,16-dimethyl Prostaglandin E1；16,16-dimethyl Prostaglandin E116,16-dimethyl Prostaglandin E1；16,16
16,16-dimethyl Prostaglandin E1 is a PGE1 (T1626) analog that induces bronchoconstriction and vascular smooth muscle contraction and inhibits indomethacin-induced cell elongation.
价 格：￥电议型 号：T36214产 地：中国大陆
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T3621316,16-dimethyl Prostaglandin D2；16,16-dimethyl Prostaglandin D216,16-dimethyl Prostaglandin D2；16,16
16,16-dimethyl PGD2 is a metabolically stable synthetic analog of PGD2. It enhances ADP-induced human platelet aggregation and increases systemic blood pressure in rats.
价 格：￥电议型 号：T36213产 地：中国大陆
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T3621216(S)-Iloprost；16(S)-Iloprost16(S)-Iloprost
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(S)-Iloprost potently inhibits platelet aggregation with an IC50 value of 3.5 nM.
价 格：￥电议型 号：T36212产 地：中国大陆
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T3621116(R)-Iloprost；16(R)-Iloprost16(R)-Iloprost
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(R)-Iloprost inhibits platelet aggregation with an IC50 value of 65 nM.
价 格：￥电议型 号：T36211产 地：中国大陆
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T3621015-keto Treprostinil (sodium salt)；15-keto Treprostinil (sodium salt)15-keto Treprostinil (sodium sa
15-keto Treprostinil is an impurity found in treprostinil , which is a stable analog of prostaglandin I2 with a longer plasma half-life. Formulations containing treprostinil are used for the treatment of primary pulmonary hypertension.
价 格：￥电议型 号：T36210产 地：中国大陆
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T3621Brigatinib；布格替尼AP-26113；布格替尼|||AP-26113
Brigatinib (AP-26113) is a highly potent and selective ALK inhibitor.
价 格：￥电议型 号：T3621产 地：中国大陆
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T35621Febuxostat Acyl Glucuronide；Febuxostat Acyl GlucuronideFebuxostat Acyl Glucuronide
Febuxostat acyl glucuronide is a metabolite of the xanthine oxidoreductase inhibitor febuxostat . Febuxostat acyl glucuronide is formed via glucuronidation of febuxostat by uridine diphosphate-glucuronosyltransferases (UGTs).
价 格：￥电议型 号：T35621产 地：中国大陆
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T35276YS 3621；化合物 T35276YS-3621|||YS3621；YS-3621|||YS3621
YS 3621 is a biochemical.
价 格：￥电议型 号：T35276产 地：中国大陆
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T35093W 6211；化合物 T35093W6211|||W-6211；W6211|||W-6211
W 6211 is a biochemical.
价 格：￥电议型 号：T35093产 地：中国大陆
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T34621Serrawettin W2；化合物 T34621Serrawettin W2
Serrawettin W2 is an extracellular cyclic lipopeptide that promotes flagellum-dependent.
价 格：￥电议型 号：T34621产 地：中国大陆
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T3445LImportazole HCl (662163-81-7 free base)；化合物 T3445LImportazole hydrochloride|||Importazole HCl|||Impo
Importazole specifically inhibits the importin-β likely by altering its interaction with RanGTP.
价 格：￥电议型 号：T3445L产 地：中国大陆
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T34328Rimexolone；化合物 T34328Rimexel|||Org-6216|||Vexol；Rimexel|||Org-6216|||Vexol
Rimexolone is a glucocorticoid steroid used to treat inflammation in the eye.
价 格：￥电议型 号：T34328产 地：中国大陆
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T32621Ledazerol；化合物 T32621Ledazerolum；Ledazerolum
Ledazerol is a vasodilator.
价 格：￥电议型 号：T32621产 地：中国大陆
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T32006GSK-2262167 sodium；化合物 T32006GSK-2262167|||GSK2262167|||GSK 2262167；GSK-2262167|||GSK2262167|||GSK 2
GSK-2262167 is a potent S1P1 agonist, as effective as fingolimod in collagen-induced arthritis models, and shows good preclinical pharmacokinetic properties.
价 格：￥电议型 号：T32006产 地：中国大陆
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T30851CGP-62198A；化合物 T30851WXF63HI1WD|||UNII-WXF63HI1WD|||SCHEMBL6042796|||CGP62198A；WXF63HI1WD|||UNII-WXF
CGP-62198A is a bio-active chemical.
价 格：￥电议型 号：T30851产 地：中国大陆
