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T10669Canagliflozin-d4；化合物 T10669Canagliflozin D4；Canagliflozin D4
Canagliflozin D4 is a deuterium-labeled Canagliflozin. Canagliflozin is an SGLT2 inhibitor.
价 格：￥电议型 号：T10669产 地：中国大陆
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T10662LCalcimycin；离子载体(钙镁盐混合物)Antibiotic A-23187|||A-23187；Antibiotic A-23187|||离子载体(钙镁盐混合物)|||A-23187
Calcimycin (A-23187) is an ionophorous, polyether carboxylic antibiotic from Streptomyces chartreusensis. It binds and transports calcium and other divalent cations across membranes and uncouples oxidative phosphorylation while inhibiting ATPase of rat liver mitochondria. The substance is used mostly as a biochemical tool to study the role of divalent cations in various biological systems.
价 格：￥电议型 号：T10662L产 地：中国大陆
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T10660LCAL-130 Hydrochloride；化合物 T10660LCAL-130 Hydrochloride
CAL-130 Hydrochloride is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660L产 地：中国大陆
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T10659Ca2+ channel agonist 1；化合物Ca2+ channel agonist 1Ca2+ channel agonist 1
Ca2+ channel agonist 1 is an agonist of N-type Ca2+ channel and an inhibitor of Cdk2 (EC50s: 14.23 μM and 3.34 μM) and is used as a potential treatment for motor nerve terminal dysfunction.
价 格：￥电议型 号：T10659产 地：中国大陆
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T1065Baclofen；巴氯芬Lioresal；巴氯芬|||Lioresal
Baclofen (Lioresal) is a synthetic chlorophenyl-butanoic acid derivative used to treat spasms due to spinal cord damage and multiple sclerosis, muscle-relaxing Baclofen acts as a gamma-aminobutyric acid (GABA) agonist specific for GABA-B receptors. It acts at spinal and supraspinal sites, reducing excitatory transmission.
价 格：￥电议型 号：T1065产 地：中国大陆
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T10649c-Fms-IN-3；化合物c-Fms-IN-3c-Fms-IN-3
c-Fms-IN-3 is a novel inhibitor of the c-FMS and can be used in studies about antirheumatic and anti-inflammatory diseases.
价 格：￥电议型 号：T10649产 地：中国大陆
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T10648c-Fms-IN-9；化合物 T10648c-Fms-IN-9
c-Fms-IN-9 is a c-FMS inhibitor. It inhibits unphosphorylated c-FMS kinase (uFMS) and uKIT (IC50s: <0.01 μM and 0.1-1 μM).
价 格：￥电议型 号：T10648产 地：中国大陆
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T10639C-021 dihydrochloride；化合物C-021 dihydrochlorideC-021 dihydrochloride
C-021 dihydrochloride is a potent CCR4 antagonist. It potently inhibits functional chemotaxis in human and mouse with IC50s of 140 nM and 39 nM.
价 格：￥电议型 号：T10639产 地：中国大陆
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T10638LAW68；化合物 AW68AW68|||AW68；AW68|||AW68
AW68 is a potential small molecule BRD4 inhibitor that prevents and treats BRD4-related diseases and can be used in cancer research.
价 格：￥电议型 号：T10638L产 地：中国大陆
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T10631LBucindolol Formate；化合物Bucindolol FormateBucindolol Formate (71119-11-4 Free base)；Bucindolol Formate
Bucindolol Formatel is a blocker of β1-adrenergic receptor. Bucindolol exhibits intrinsic sympathomimetic activity. Bucindolol can be used in the research of heart failure.
价 格：￥电议型 号：T10631L产 地：中国大陆
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T10629Btk inhibitor 2；化合物Btk inhibitor 2BGB-3111 analog；BGB-3111 analog
Btk inhibitor 2 (BGB-3111 analog) is a BTK inhibitor.
价 格：￥电议型 号：T10629产 地：中国大陆
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T10626(Rac)-IBT6A；化合物(Rac)-IBT6A(Rac)-IBT6A
(Rac)-IBT6A is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib and can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct.
价 格：￥电议型 号：T10626产 地：中国大陆
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T10625L(Rac)-IBT6A hydrochloride (1412418-47-3 free base)；化合物 T10625L(Rac)-IBT6A hydrochloride；(Rac)-IBT6A
(Rac)-IBT6A hydrochloride is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib. IBT6A can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a Btk inhibitor (IC50: 0.5 nM).
价 格：￥电议型 号：T10625L产 地：中国大陆
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T10619Bromelain；菠萝蛋白酶Bromelain
Bromelain is an anti-inflammatory drug derived from pineapple stem. It acts through down-regulation of plasma kininogen, degradation of advanced glycation end-product receptors, inhibition of Prostaglandin E2 expression, and regulation of angiogenic biomarkers as well as antioxidant action upstream in the COX-pathway.
价 格：￥电议型 号：T10619产 地：中国大陆
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T10617Brofaromine；化合物 T10617CGP 11305A；CGP 11305A
Brofaromine (CGP 11305A) is an MAO inhibitor (IC50: 0.2 μM for MAO-A).
价 格：￥电议型 号：T10617产 地：中国大陆
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T10613BRL 37344 sodium；化合物 T10613BRL 37344A；BRL 37344A
BRL 37344 sodium is a specific agonist of the β3-adrenergic receptor. The treatment of BRL 37344 sodium significantly lowers the bodyweight of obese mice.
价 格：￥电议型 号：T10613产 地：中国大陆
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T10609Brevetoxin-3；化合物 T10609PbTx-3；PbTx-3
Brevetoxin-3 (PbTx-3) is a potent allosteric voltage-gated Na+ channel activator. Brevetoxin-3 has a high affinity to site 5 of the voltage-sensitive Na+ channels, inhibits the inactivation of Na+ channels.
价 格：￥电议型 号：T10609产 地：中国大陆
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T10603BRD-6929；化合物BRD-6929BRD-6929
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: ?1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1.5 nM) [2]. BRD-6929 potentiates the efficacy of gnidimacrin (a PKC Agonist) against latent HIV-1. BRD-6929 can be used for mood-related behavioral model research[3].
价 格：￥电议型 号：T10603产 地：中国大陆
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T10602LBRD 4354；化合物BRD 4354BRD 4354
BRD 4354 is an inhibitor of HDAC5 and HDAC9. For HDAC5 and HDAC9, the IC50s values are 0.85 and 1.88 μM, respectively.
价 格：￥电议型 号：T10602L产 地：中国大陆
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T10599BRAF inhibitor；化合物BRAF inhibitorBRAF inhibitor
BRAF inhibitor is an inhibitor of B-Raf.
价 格：￥电议型 号：T10599产 地：中国大陆
