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T13533Aflatoxin G2黄曲霉毒素 G2黄曲霉毒素 G2
Aflatoxin G2 is a major naturally produced aflatoxin. It is a mycotoxin produced by the fungi Aspergillus flavus and Aspergillus parasiticus.
价 格：￥电议型 号：T13533产 地：中国大陆
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T13530AF40431化合物 T13530AF-40431|||AF40431
AF40431 is the first reported small-molecule ligand of sortilin (IC50: 4.4 μM; Kd: 0.7 μM). AF40431 is bound in the neurotensin-binding site of sortilin.
价 格：￥电议型 号：T13530产 地：中国大陆
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T135165-Methyltetrahydrofolic acid；甲基叶酸盐5-Methyl THF；甲基叶酸盐|||5-Methyl THF
5-Methyltetrahydrofolic acid (5-Methyl THF) is a biologically active form of folic acid and a methylated derivate of tetrahydrofolate. It is the predominant natural dietary folate and the principal form of folate in plasma and cerebrospinal fluid.
价 格：￥电议型 号：T13516产 地：中国大陆
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T1351H-Lys(Tfa)-OH；化合物 H-Lys(Tfa)-OHH-Lys(Tfa)-OH
H-Lys(Tfa)-OH is an inhibitor of L-lysine cyclodeaminase.
价 格：￥电议型 号：T1351产 地：中国大陆
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T134963-?Furfuryl 2-?pyrrolecarboxylate；化合物 T134963-?Furfuryl 2-?pyrrolecarboxylate
3-Furfuryl 2-pyrrolecarboxylate, a chemical compound, is extracted from the root tuber of Pseudostellaria heterophylla.
价 格：￥电议型 号：T13496产 地：中国大陆
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T1349025,26-Dihydroxyvitamin D3；化合物 T1349025,26-Dihydroxycholecalciferol；25,26-Dihydroxycholecalciferol
25,26-Dihydroxyvitamin D3 is a metabolite of vitamin D3 with intestinal calcium transport activity.
价 格：￥电议型 号：T13490产 地：中国大陆
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T13495-Fluorouridine；5-氟尿嘧啶核苷5-Fluorouridine
5-fluorouridine is also known as FUrd, 5-Fluorouracil 1-beta-D-ribofuranoside, 5-Fur, or 5-Fluoro-uridine. 5-fluorouridine is a solid. This compound belongs to the pyrimidine nucleosides and analogues. These are compounds comprising a pyrimidine base attached to a sugar. 5-fluorouridine is known to target uridine phosphorylase. FUrd is often used in chemical and biochemical comparison studies with fluorouracil and thymine analogs.
价 格：￥电议型 号：T1349产 地：中国大陆
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T134882-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide；化合物 T134882-_E-2-decenoylamino_ethyl_2-_cyclo
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound known to inhibit stress-induced ulcers, effectively maintaining the levels of phospholipase A2 and prostaglandin E2 in rats subjected to water immersion-restrained stress-induced ulceration.
价 格：￥电议型 号：T13488产 地：中国大陆
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T13480L(S)-(-)-5-Fluorowillardiine hydrochloride；化合物 T13480L(S)-5-Fluorowillardiine hydrochloride|||(5S)-Fl
(S)-(-)-5-Fluorowillardiine hydrochloride is a potent and specific agonist of AMPAR.
价 格：￥电议型 号：T13480L产 地：中国大陆
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T13480(S)-(-)-5-Fluorowillardiine；5-氟代尿嘧啶丙氨酸(S)-5-Fluorowillardiine|||(5S)-Fluorowillardiine；(S)-5-Fluorow
(S)-(-)-5-Fluorowillardiine ((S)-5-Fluorowillardiine) is an AMPA receptor-specific agonist
价 格：￥电议型 号：T13480产 地：中国大陆
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T13473Lαvβ1 integrin-IN-1 TFA (1689540-62-2 free base)；化合物 T13473Lαvβ1 integrin-IN-1 TFA；αvβ1 integrin-IN-1
αvβ1 integrin-IN-1 TFA is an effective and selective αvβ1 integrin inhibitor (IC50: 0.63 nM).
价 格：￥电议型 号：T13473L产 地：中国大陆
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T13460(+)-Cevimeline hydrochloride hemihydrate；化合物 T13460(+)-AF102B hydrochloride hemihydrate|||(+)-SNI-20
(+)-Cevimeline hydrochloride hemihydrate ((+)-SNI-2011), a potent muscarinic receptor agonist, stands as a promising therapeutic candidate for treating xerostomia in Sjogren´s syndrome. This compound has demonstrated a broad pharmacological profile across various systems including gastrointestinal, urinary, and reproductive, in animal models such as mice, rats, guinea pigs, rabbits, and dogs. Its metabolism was assessed in vitro using rat and dog liver microsomes, revealing that (+)-SNI-20
价 格：￥电议型 号：T13460产 地：中国大陆
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T13457(Z)-9-Propenyladenine；(Z)-替诺福韦酯杂质(Z)-Mutagenic Impurity of Tenofovir Disoproxil；(Z)-替诺福韦酯杂质|||(Z)-Mu
(Z)-9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.
价 格：￥电议型 号：T13457产 地：中国大陆
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T13445(R)-Q-VD-OPh；化合物 T13445(R)-Quinoline-Val-Asp-Difluorophenoxymethylketone|||(R)-QVD-OPH；(R)-Quinoline
(R)-Q-VD-OPh is the less active enantiomer of Q-VD-OPha. Q-VD-OPha is an irreversible inhibitor of pan-caspase, with potent antiapoptotic properties.
价 格：￥电议型 号：T13445产 地：中国大陆
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T13429α-2,3-sialyltransferase-IN-1；化合物 T13429Lith-O-Asp analog；Lith-O-Asp analog
α-2,3-sialyltransferase-IN-1 is a noncompetitive inhibitor of α-2,3-sialyltransferase(IC50 of 6 μM).
价 格：￥电议型 号：T13429产 地：中国大陆
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T13427(3S,4R)-Tofacitinib；(3S,4R)-托法替尼(3S,4R)-Tofacitinib
(3S,4R)-Tofacitinib is an less active enantiomer of Tofacitinib. Tofacitinib is a JAK3 inhibitor(IC50 : 1 nM).
价 格：￥电议型 号：T13427产 地：中国大陆
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T13426L(3S,4S)-Tofacitinib(3S,4S)-托法替尼(3S,4S)-托法替尼
(3S,4S)-Tofacitinib, a less active enantiomer of tofacitinib, is a Janus kinases inhibitor.
价 格：￥电议型 号：T13426L产 地：中国大陆
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T13421(-)-Cevimeline hydrochloride hemihydrate；化合物 T13421(-)-SNI-2011|||(-)-AF102B hydrochloride hemihydra
Cevimeline hydrochloride hemihydrate ((-)-SNI-2011), a novel muscarinic receptor agonist, is being explored as a potential treatment for xerostomia in Sjogren´s syndrome, exhibiting an IC50 value indicative of its affinity for mAChR. This compound´s pharmacological effects on the gastrointestinal, urinary, and reproductive systems, alongside its impact on various tissues, were thoroughly examined in species including mice, rats, guinea pigs, rabbits, and dogs. The metabolic breakdown
价 格：￥电议型 号：T13421产 地：中国大陆
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T13418CP-319340(free base)；化合物 T13418CP-319340(free base)
CP-319340 free base is a inhibitor of microsomal triglyceride transfer protein (MTP) .
价 格：￥电议型 号：T13418产 地：中国大陆
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T13412LZM223 hydrochloride (2031177-48-5 free base)；化合物 T13412LZM223 hydrochloride；ZM223 hydrochloride
ZM223 hydrochloride is an orally active, potent non-covalent inhibitor of NEDD8 activating enzyme (NAE), and with excellent anticancer activity.
价 格：￥电议型 号：T13412L产 地：中国大陆
