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T22781LFFN 511 hydrochloride；FFN 511 盐酸盐FFN 511 hydrochloride(1004548-96-2 Free base)；FFN 511 hydrochloride
FFN 511 hydrochloride is a fluorescent pseudo-neurotransmitters (FFNs) targeting neuronal vesicular monoamine transporter 2 (VMA T2).FFN 511 hydrochloride inhibits the binding of 5-hydroxytryptamine to VMA T2-containing membranes and can be used for labelling of dopaminergic nerve endings in acute slices of in vivo cortex-striatum. The excitation and emission maxima are 406 and 501 nm, respectively.
价 格：￥电议型 号：T22781L产 地：中国大陆
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T22697CS 2100；化合物CS 21001-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azeti
CS 2100 (1-[[4-Ethyl-5-[5-(4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-2-thienyl]methyl]-3-azetidinecarboxylic acid) is an S1P1 agonist.
价 格：￥电议型 号：T22697产 地：中国大陆
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T2269Pirinixic Acid；匹立尼酸Wy-14643|||NSC 310038；Wy-14643|||NSC 310038|||匹立尼酸
Pirinixic Acid (NSC 310038) is a synthetic thiacetic acid derivative used in biomedical research, carcinogenic Pirinixic acid is a peroxisome proliferator that activates specific peroxisome proliferator-activated receptors (PPAR).
价 格：￥电议型 号：T2269产 地：中国大陆
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T22680CP-100356 hydrochloride；CP-100356 盐酸盐CP-100356 HCl|||CP 100356 hydrochloride；CP-100356 HCl|||CP 1003
CP-100356 hydrochloride is an orally active and low micromolar dual inhibitor of MDR1 (P-gp) and BCRP, a nucleotide-derived substrate analogue with inhibitory effects on MDR1-mediated Calcein-AM transporter and BCRP-mediated Prazosin transporter.CP-100356 Inhibits OATP1B1, induces stomatal opening in the dark.
价 格：￥电议型 号：T22680产 地：中国大陆
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T22612BMY-14802 hydrochloride；化合物BMY-14802盐酸盐BMS 181100 hydrochloride|||BMY-14802-1|||BMY 14802 hydrochlor
BMY-14802 hydrochloride (BMS 181100 hydrochloride) is a selective antagonist of σ receptor (IC50 = 112 nM) with antipsychotic effects. BMY-14802 hydrochloride is an agonist of the α1-adrenergic receptor and 5-HT1A.
价 格：￥电议型 号：T22612产 地：中国大陆
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T22359MDL 100009；化合物MDL 100009MDL 100009
MDL 100009, the S-enantiomer of MDL 100151 and the opposite enantiomer of MDL 100907, is a selective antagonist of 5-HT2A.
价 格：￥电议型 号：T22359产 地：中国大陆
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T22062CCG-100602；化合物CCG-100602CCG-100602
CCG-100602 inhibits RhoA/C-mediated, SRF-driven luciferase expression in PC-3 prostate cancer cells (IC50 :9.8 μM).
价 格：￥电议型 号：T22062产 地：中国大陆
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T21788BD 1008 dihydrobromide；N-[2-(3,4-二氯苯基)乙基]-N-甲基-1-吡咯烷乙胺二氢溴酸盐BD 1008 dihydrobromide
BD 1008 dihydrobromide is a selective antagonist of the sigma 1 (σ1) receptor (Ki = 2 nM). BD 1008 dihydrobromide have high affinity for sigma1 receptors, moderate affinity for sigma2 receptors.
价 格：￥电议型 号：T21788产 地：中国大陆
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T21600MPC-3100；化合物 T21600MPC-3100
MPC-3100 is an orally bioavailable, synthetic, second-generation small-molecule inhibitor of Hsp90 with significant antitumor activity [1].
价 格：￥电议型 号：T21600产 地：中国大陆
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T21561WAY-100635；化合物 T21561WAY-100635
WAY-100635 is a potent and selective 5-hydroxytryptamine 1A (5-HT1A) receptor antagonist with an IC50 of 0.91 nM and Ki of 0.39 nM. It exhibits pIC50 values of 8.9 and 6.6 for 5-HT1A and α1-adrenergic receptors, respectively. Moreover, WAY-100635 acts as a potent agonist of the dopamine D4 receptor [1] [2] [3].
价 格：￥电议型 号：T21561产 地：中国大陆
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T21453AP-24600；化合物 T21453OZ477A282R|||AP 24600|||DA-12847|||KB-310048|||UNII-OZ477A282R；OZ477A282R|||AP 24
AP-24600 is a bio-active chemical.
价 格：￥电议型 号：T21453产 地：中国大陆
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T21387Nafoxidine HCl（1845-11-0 Free base）；化合物Nafoxidine HCl（1845-11-0 Free base）PNU-0011100|||PNU0011100||
Nafoxidine is a partial estrogen antagonist. It inhibits angiogenesis in some tissues by blocking the effects of VEGF and FGF; paradoxically, it may enhance angiogenesis in uterine tissue. Nafoxidine also induces calcium signaling, oxidative stress, and protein kinase C.
价 格：￥电议型 号：T21387产 地：中国大陆
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T21294Polmacoxib；帕马考昔CG-100649|||CG100649|||CG 100649；CG-100649|||帕马考昔|||CG100649|||CG 100649
Polmacoxib (CG 100649) is a first-in-class NSAID drug candidate, is a dual inhibitor of carbonic anhydrase (CA) and COX-2. Polmacoxib inhibits premalignant and malignant colorectal lesions in mouse models, partly through inhibiting tumor cell proliferation.
价 格：￥电议型 号：T21294产 地：中国大陆
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T21100Dodecanedinitrile；化合物 T211001,10-Decamethylenedinitrile|||Decamethylenedinitrile|||1,12-Dodecanedini
Dodecanedinitrile is a bioactive chemical.
价 格：￥电议型 号：T21100产 地：中国大陆
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T21039PL 100；化合物 T21039MK-8122|||PL-100|||PPL-100|||PPL 100|||MX-100；MK-8122|||PL-100|||PPL-100|||PPL 100|
PL 100 could inhibit HIV-1 protease.
价 格：￥电议型 号：T21039产 地：中国大陆
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T21009Conjugated linoleic acid；化合物 T21009Conjugated linoleic acid
Conjugated linoleic acid, a naturally occurring fatty acid, is present in ruminant meat and dairy products and is produced by a bio-hydrogenation process in the rumen. In this case, the predominant isomer formed is 9cis, 11trans.
价 格：￥电议型 号：T21009产 地：中国大陆
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T21008Deacetyldiltiazem；化合物 T21008Desacetyl Diltiazem；Desacetyl Diltiazem
Deacetyldiltiazem is a metabolite product of Diltiazem which is a coronary vasodilator, and is present in the plasma of individuals taking Diltiazem.
价 格：￥电议型 号：T21008产 地：中国大陆
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T21007m 15；化合物 T210075COB|||5OCB|||D 105；5COB|||5OCB|||D 105
M 15 liquid crystals are a member of the oxycyanobiphenyl family, which exhibits a liquid crystalline phase in the temperature range of 47-67.5℃.
价 格：￥电议型 号：T21007产 地：中国大陆
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T21006Deacetyl-7-aminocephalosporanic acid；化合物 T21006Deacetyl-7-aminocephalosporanic acid
Deacetyl-7-aminocephalosporanic acid, an intermediate in the synthesis of semi-synthetic cephalosporins, is found in Acremonium chrysogenum.
价 格：￥电议型 号：T21006产 地：中国大陆
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T21005Lupulon；化合物 T21005Lupulon
Lupulon has a role as an apoptosis inducer, antimicrobial agent, angiogenesis inhibitor, and antineoplastic agent.
价 格：￥电议型 号：T21005产 地：中国大陆
