当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3882664
自主品牌
已选条件
-
T28451Prodilidine hydrochloride；化合物 T28451ARC I-O-1|||A-1981-12|||CI-427|||Prodilidine HCl|||CI 427；ARC I-
Prodilidine hydrochloride is an opioid analgesic.
价 格：￥电议型 号：T28451产 地：中国大陆
-
T28437LPomisartan 2HCl；泊米沙坦盐酸盐Pomisartan 2HCl(144702-17-0 Free base)|||BIBR363 2HCL；Pomisartan 2HCl(144702-
Pomisartan 2HCl (BIBR363 2HCL) is a small molecule AT1R antagonist used to study heart failure and hypertension.
价 格：￥电议型 号：T28437L产 地：中国大陆
-
T28433PNU-142731A HCl；化合物 T28433PNU142731A|||PNU 142731A|||PNU-142731A；PNU142731A|||PNU 142731A|||PNU-1427
PNU-142731A HCl, a mediator release inhibitor and an IL-5 production inhibitor, is used potentially for the treatment of asthma.
价 格：￥电议型 号：T28433产 地：中国大陆
-
T28417Pipamperone HCl；化合物 T28417fluoropipamide|||floropipamide hydrochloride|||carpiperone|||floropipamide
Pipamperone acts as an antagonist of the 5-HT2A, 5-HT2B, 5-HT2C D2, D3, D4, α1-adrenergic, and α2-adrenergic receptors. It shows much higher affinity for the 5-HT2A and D4 receptors over the D2 receptor (15-fold in the case of the D4 receptor, and even higher in the case of the 5-HT2A receptor), being regarded as "highly selective" for the former two sites at low doses. Pipamperone has low and likely insignificant affinity for the H1 and mACh receptors, as well as for other serotonin a
价 格：￥电议型 号：T28417产 地：中国大陆
-
T28404Phenyramidol Hydrochloride；化合物 T28404Vazalmin|||Analexin|||Firmalgil|||Phenyramidol HCl|||Betapirin；
Phenyramidol Hydrochloride is an anticoagulant and analgesic.
价 格：￥电议型 号：T28404产 地：中国大陆
-
T28388PF-5274857 mseylate (1373615-35-0 free base)；化合物 T28388PF5274857 HCl|||PF 5274857|||PF-5274857|||PF-
PF-5274857 is a potent, orally active and selective inhibitor of hedgehog (Hh) signaling pathway (IC50 = 5.8 nM, Ki = 4.6 nM) . PF-5274857 effectively penetrates the blood-brain barrier and inhibits Smo activity in the brain of primary medulloblastoma mice, resulting in improved animal survival rates.
价 格：￥电议型 号：T28388产 地：中国大陆
-
T28376PF-06758955 HCl；化合物 T28376PF6758955|||PF 06758955|||PF06758955|||PF 6758955 HCl|||PF-06758955|||PF-6
PF-06758955 is a potent, MAP4K4-selective inhibitor.
价 格：￥电议型 号：T28376产 地：中国大陆
-
T28368PF-04859989 HCl化合物PF-04859989PF 04859989|||PF04859989|||PF-04859989HCl|||PF-04859989
PF-04859989 HCl is a brain-penetrable and irreversible inhibitor of kynurenine amino transferase II (KAT II), which is the enzyme responsible for most of the brain synthesis of kynurenic acid.
价 格：￥电议型 号：T28368产 地：中国大陆
-
T28364PF-03463275 2HCl；化合物 T28364PF3463275|||PF 3463275|||PF03463275|||PF-3463275；PF3463275|||PF 3463275||
PF-03463275 is an orally available, CNS-penetrant inhibitor of SLC6A9, a GlyT1 glycine transporter.
价 格：￥电议型 号：T28364产 地：中国大陆
-
T28346PD-217014 HCl；化合物 T28346PD 217014|||PD217014|||PD-217,014|||PD-217014；PD 217014|||PD217014|||PD-217,
PD-217014 is a GABA analog. It inhibits (3)H-gabapentin binding to alpha(2)delta subunit of voltage-gated calcium channels in a concentration-dependent manner (K(i) = 18 nmol/l). PD-217014 possesses visceral analgesic activity.
价 格：￥电议型 号：T28346产 地：中国大陆
-
T28297Parsaclisib hydrochloride；化合物Parsaclisib HClParsaclisib HCl|||INCB-50465|||INCB 050465|||INCB-050465
Parsaclisib hydrochloride (INCB050465 HCl) is a selectve PI3Kδ inhibitor with antitumor activity. Parsaclisib demonstrates potent activity with IC50 values ranging from 0.2 to 2 nM.
价 格：￥电议型 号：T28297产 地：中国大陆
-
T28287PA1 2HCl；化合物 T28287PA1|||PA1 dihydrochloride；PA1|||PA1 dihydrochloride
PA1 2HCl is a blocker of photoswitchable epithelial sodium channel (ENaC). PA1 2HCl enables the optical control of ENaC channels, in particular the δβγ isoform, by switching between blue and green light, or by turning on and off blue light.
价 格：￥电议型 号：T28287产 地：中国大陆
-
T28273LOT-551 HCl；OT-551盐酸盐OT-551 HCl（627085-11-4 Free base）；OT-551 HCl（627085-11-4 Free base）
OT-551 HCl is an NF-Κb inhibitor, a disubstituted hydroxylamine with antioxidant properties can be used for the treatment of cataracts and age-related macular degeneration and geographic atrophy (GA).
价 格：￥电议型 号：T28273L产 地：中国大陆
-
T28270Osemozotan HCl；奥莫佐坦MCI-242|||MN-305|||Osemozotan hydrochloride|||MKC-242|||MKC242|||MCI242；MCI-242||
Osemozotan HCl (Osemozotan hydrochloride) is a novel and selective 5-HT1A receptor agonist that reduces methamphetamine-induced c-Fos expression in the medial prefrontal cortex and striatum.Osemozotan HCl is used in the study of mechanical abnormalities of pain and depression.
价 格：￥电议型 号：T28270产 地：中国大陆
-
T28247ONO-1714 HCl；化合物 T28247ONO-1714|||ONO1714|||ONO-1714 hydrochloride|||ONO 1714；ONO-1714|||ONO1714|||O
ONO-1714 is a inducible nitric oxide synthase (NOS-2) inhibitor. ONO-1714 reduces hyperoxic lung injury in mice. ONO-1714 attenuates inflammation-related large bowel carcinogenesis in male Apc(Min/+) mice. ONO-1714 also inhibits neuronal NOS and exerts antinociception in rats.
价 格：￥电议型 号：T28247产 地：中国大陆
-
T28229Olanexidine hydrochloride；盐酸奥兰西丁OPB2045|||OPB-2045|||OPB-2045 HCl|||OPB 2045；OPB2045|||OPB-2045|||OP
Olanexidine hydrochloride (OPB-2045 HCl) shows bactericidal activity against Gram-positive and Gram-negative bacteria. Olanexidine hydrochloride disrupts the membrane integrity of S. aureus.
价 格：￥电议型 号：T28229产 地：中国大陆
-
T28202NSC-152035；化合物 T28202Racemetirosine methyl ester HCl|||NSC 152035|||Racemetirosine methyl ester hydr
NSC-152035 is an inhibitor of tyrosine 3-monooxygenase.
价 格：￥电议型 号：T28202产 地：中国大陆
-
T28189Nortopixantrone HCl；诺托生琼盐酸盐BBR3438|||Nortopixantrone hydrochloride|||BBR-3438；BBR3438|||Nortopixantr
Nortopixantrone HCl (BBR 3438) is a novel 9-azacyclonopyrazole that shows antitumor activity in a human prostate cancer model.
价 格：￥电议型 号：T28189产 地：中国大陆
-
T28172Niguldipine hydrochloride；化合物 T28172BY-935|||Niguldipine HCl|||B-85935|||B-8509-035|||B-859-35；BY-93
Niguldipine is a calcium channel antagonist. Niguldipine shows high affinity to Ca2+ channels and to a subtype of alpha 1-adrenoceptors.
价 格：￥电议型 号：T28172产 地：中国大陆
-
T28167NGB 2904；化合物NGB2904 HClNGB2904 HCl|||NGB-2904|||NGB2904；NGB2904 HCl|||NGB-2904|||NGB2904
NGB 2904 is a potent and selective antagonist of dopamine D3 receptor (Ki values are 1.4, 217, 223, 642, > 5000, > 10000 and > 10000 nM for D3, D2, 5-HT2, α1, D4, D1 and D5 receptors respectively). NGB2904 potently antagonizes mitogenesis stimulated by quinpirole (IC50 = 6.8 nM).
价 格：￥电议型 号：T28167产 地：中国大陆
