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T10058A2B receptor antagonist 1A-2B receptor antagonist 1,A2B receptor antagonist 1
A2B receptor antagonist 1 (EXAMPLE 9B) is a potent A2B adenosine receptor antagonist extracted from patent WO 2009157938 A1.
价 格：￥电议型 号：T10058产 地：中国大陆
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T7338DHBP dibromideCa channels,inhibit,DHBP dibromide,Inhibitor,Ca2+ channels,Calcium Channel
DHBP dibromide is calcium release and a muscle relaxant inhibitor.
价 格：￥电议型 号：T7338产 地：中国大陆
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TN70872,5-dimethoxycyclohexa-2,5-diene-1,4-dio2,5dimethoxycyclohexa2,5diene1,4dio,2,5 dimethoxycyclohexa 2
2,5-dimethoxycyclohexa-2,5-diene-1,4-dio is a natural product. The redox cycle of 2,5-dimethoxybenzoquinone is a source of reducing equivalent for the regeneration of Fe2+ and H2O2 in brown rot fungal decay of wood.
价 格：￥电议型 号：TN7087产 地：中国大陆
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TQ0033ZegocractinInhibitor,inhibit,Calcium release-activated channels,Ca2+ release-activated Ca2+ channels
CM4620 is a calcium-release activated calcium-channel (CRAC channel) inhibitor.
价 格：￥电议型 号：TQ0033产 地：中国大陆
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T8944TTA-A2Pregnane X receptor,TTA-A2,neurological diseases,T-type calcium channel,Inhibitor,Ca2+ channel
TTA-A2 is a selective T-type calcium channel antagonist as a potent anticonvulsant that the Cav3.1 isoform plays a prominent role in mediating. TTA-A2 is equally potent against the Cav3.1 (a1G) and Cav3.2 (a1H) channels with IC50 values of 89 nM and 92 nM, respectively, at -80 and -100 mV holding potentials. TTA-A2 can be used for the research of a variety of human neurological diseases, including sleep disorders and epilepsy.
价 格：￥电议型 号：T8944产 地：中国大陆
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T10212A2AR-agonist-1
A2AR-agonist-1 is a potent A2AR and ENT1 agonist (Ki: 4.39 and 3.47 for A2AR and ENT1. It targets the Adenosine A2A Receptor and Adenosine Transporter for Neuroprotection.
价 格：￥电议型 号：T10212产 地：中国大陆
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T11665Ionomycin calciumCa2+ channels,PKC,ionophore,Calcium Channel,Ionomycin,SQ 23377,Ionomycin calcium,An
lonomycin calcium is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. also induces the activation of protein kinase C (PKC). Ionomycin calcium is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionomycin promotes apoptosis.
价 格：￥电议型 号：T11665产 地：中国大陆
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T7373CDN1163Inhibitor,CDN 1163,Calcium Channel,Ca channels,Ca2+ channels,CDN-1163,CDN1163,inhibit
CDN1163 is a small molecule activator of sarco/endoplasmic reticulum Ca2+-ATPase (SERCA).
价 格：￥电议型 号：T7373产 地：中国大陆
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T8674SR33805Ca channels,channel,failing,Ca2+ channels,Ca2+,SR 33805,Calcium Channel,acute,L-type,SR-33805
SR33805 is a potent antagonist of Ca2+ channel(EC50s of 4.1 nM and 33 nM in depolarized and polarized conditions, respectively)
价 格：￥电议型 号：T8674产 地：中国大陆
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TP1549LNY-BR-1 p904 A2 acetate(347142-73-8 free base)NY-BR-1 p-904 A2 acetate(347142-73-8 free base),NYBR1
T-cell clones specific for this NY-BR-1 epitope (p904) can recognize breast tumor cells expressing NY-BR-1.
价 格：￥电议型 号：TP1549L产 地：中国大陆
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T216531,4-DPCAHIF-PH,HIF/HIF Prolyl-Hydroxylase,HIF-1α,HIFs,FIH,P4HA1,P4HA2,1,4DPCA,healing,Inhibitor,Hypo
1,4-DPCA is an inhibitor of prolyl-hydroxylase with an IC50 of 2.4 ?M for collagen hydroxylation in human foreskin fibroblasts and 60 μM for factor inhibiting HIF (FIH).
价 格：￥电议型 号：T21653产 地：中国大陆
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T6S1418Praeruptorin CCa2+ channels,Ca channels,Calcium Channel,Praeruptorin C,Inhibitor,inhibit
1. Praeruptorin C has been widely used as an antioxidant and a calcium antagonist to treat diseases. 2. Praeruptorin C partially protects cortical neurons by inhibiting the expression of GluN2B-containing NMDA receptors and regulating the Bcl-2 family. 3. Praeruptorin C can reduce vascular hypertrophy in isolated rat hypertrophied smooth muscle cells, and this is associated with improvement of smooth muscle cells [Ca2+]i level, nitric oxide content and cellular signal transdution of protein kina
价 格：￥电议型 号：T6S1418产 地：中国大陆
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T2782CatharanthineCalcium Channel,Ca2+ channels,Ca channels,Inhibitor,Catharanthine,inhibit
Catharanthine suppresses nicotinic receptor-mediated diaphragm contractions (IC50=59.6 μM).
价 格：￥电议型 号：T2782产 地：中国大陆
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TWA2417Sodium taurocholateI nterleukin-1β,Tumor necrosis factor-α,inhibit,Sodium taurocholate hydrate,Immun
Taurocholic acid is the main end product of cholesterol catabolism. During enterohepatic circulation, bile taurocholic acid is converted by the microorganisms to taurodeoxycholic acid and deoxycholic acid.[3] These are reabsorbed by the liver via a carrier-mediated process and converted by liver enzymes to taurocholic acid.
价 格：￥电议型 号：TWA2417产 地：中国大陆
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TP1367[D-Ala2]leucine-enkephalinOpioid Receptor,[DAla2]leucineenkephalin,Inhibitor,[D Ala2]leucine enkepha
[D-Ala2]-Leucine enkephalin is a delta opioid agonist used to study the signaling pathway of delta opioid receptors.
价 格：￥电议型 号：TP1367产 地：中国大陆
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T67868Oleana-2,12-dien-28-oic acidOleana2,12dien28oicacid
Oleana-2,12-dien-28-oic acid is an HBsAg and HBeAg inhibitor that obviously inhibit HBV deoxyribonucleic acid (HBV-DNA) replication in HepG2.2.15 cells. Oleana-2,12-dien-28-oic acid for the study of hepatitis B virus infection.
价 格：￥电议型 号：T67868产 地：中国大陆
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TQ0108MK-6892HCAR2,PUMA-G,MK-6892,HM74A,HCA2,Inhibitor,GPR109A,MK6892,inhibit,MK 6892
MK-6892 is a selective and full agonist for the high-affinity nicotinic acid receptor GPR109A (Ki: 4 nM; GTPγS EC50: 16 nM).
价 格：￥电议型 号：TQ0108产 地：中国大陆
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T7550BarnidipineBarnidipine,Inhibitor,Ca2+ channels,Calcium Channel,inhibit,Ca channels
Barnidipine is a calcium channel blocker.
价 格：￥电议型 号：T7550产 地：中国大陆
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T8863VK-II-36Calcium Channel,VKII36,Ca channels,Ca2+ channels,Inhibitor,inhibit,VK II 36
VK-II-36, a carvedilol analog, suppresses sarcoplasmic reticulum (SR) Ca(2+) release but does not block the β-receptor.
价 格：￥电议型 号：T8863产 地：中国大陆
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T6625Ozagrel hydrochlorideOKY-046,Inhibitor,thromboxane A2,TXA2,antiplatelet,OKY 046,Ozagrel,aggregation,
Ozagrel HCl is a selective thromboxane A(2) synthetase inhibitor used for the improvement of postoperative cerebrovascular contraction and accompanying cerebral ischaemia.
价 格：￥电议型 号：T6625产 地：中国大陆
