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：3723018
自主品牌
已选条件
-
TP1994LM871 acetateM871 acetate,M-871 acetate(908844-75-7 Free base)
M871 acetate is a selective galanin GAL2 receptor antagonist (Ki values are 13.1 and 420 nM at GAL2 and GAL1 receptors, respectively).It blocks pronociceptive effects of GAL2 agonists including AR-M1896.
价 格：￥电议型 号：TP1994L产 地：中国大陆
-
T8742G5-7antiangiogenic,inhibit,Apoptosis,JAK,Glioma,G-5-7,cycle,G5 7,phase,G57,STAT3,cell,Inhibitor,EGFR
JAK2 inhibitor G5-7 is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for glioma study
价 格：￥电议型 号：T8742产 地：中国大陆
-
TP1862L[Sar9] Substance P acetate(77128-75-7 free base)[Sar9] Substance P acetate(77128 75 7 free base),[Sa
[Sar9]-Substance P acetate is one of NK-1 receptor agonist. The action of SP on progesterone metabolism was mimicked by the rNK1-specific agonist [Sar-9,Met(O2)11]-SP.
价 格：￥电议型 号：TP1862L产 地：中国大陆
-
T4444A-674563 HCl (552325-73-2(free base))A 674563 HCl (552325 73 2(free base)),A674563 HCl (552325732(fr
A-674563 is an orally available, ATP-competitive, and reversible inhibitor of Akt (Ki: 11 nM for Akt1) [1]. It exhibits inhibitory activity against PKA and Cdk2 (IC50: 16/46 nM) but is 10- to >1, 800-fold selective for Akt1 versus additional kinases in the CMGC, CAMK, and TK families [1].
价 格：￥电议型 号：T4444产 地：中国大陆
-
T8945LAST5902 mesylate(2412155-74-7 free base)AST-5902 mesylate(2412155-74-7 free base),AST5902 mesylate(2
AST5902 mesylate is principal metabolite of Alflutinib in vivo. AST5902 mesylate exerts antineoplastic activity.
价 格：￥电议型 号：T8945L产 地：中国大陆
-
TP1600LIα52 acetate(137756-45-7 free base)Iα52 acetate(137756457 free base),Iα52 acetate(137756 45 7 free b
Iα52 acetate is a naturally processed peptide encompassed the residues 52-68 of the murine I-Eα chain and may contribute to selection of immature T cells.
价 格：￥电议型 号：TP1600L产 地：中国大陆
-
TP1363LNeurokinin B acetate(86933-75-7 free base)Neurokinin B acetate(86933757 free base),Neurokinin B acet
Neurokinin B acetate is the acetate form of Neurokinin B, which belongs to the tachykinin family. Neurokinin binds to neurokinin receptor 1 (NK1R), nk2r and NK3R, and mediates its biological effects.
价 格：￥电议型 号：TP1363L产 地：中国大陆
-
T6139LA-674563 2HCl(552325-73-2(fb-2hcl))
A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.
价 格：￥电议型 号：T6139L产 地：中国大陆
-
T4690Betrixaban hydrochloride(330942-05-7(free base))盐酸贝曲西班；PRT054021 hydrochloride
Betrixaban is a potent, selective, and orally efficacious factor Xa (fXa) inhibitor (IC50: 1.5 nM).
价 格：￥电议型 号：T4690产 地：中国大陆
-
T4122TAPI-1 trifluoroacetate (171235-71-5(free base))
TAPI-1 is an ADAM17/TACE inhibitor, which blocks shedding of cytokine receptors.
价 格：￥电议型 号：T4122产 地：中国大陆
-
T22574LAngiotensin 1/2 (5-7) acetate
Angiotensin 1/2 (5-7) acetate is a peptide with the sequence H2N-Ile-His-Pro-OH. Angiotensin is an oligopeptide and is a hormone and a powerful dipsogen. It is derived from the precursor molecule angiotensinogen, a serum globulin produced in the liver. It
价 格：￥电议型 号：T22574L产 地：中国大陆
-
T8742G5-7；化合物JAK2 inhibitor G5-7JAK2 inhibitor G5-7；JAK2 inhibitor G5-7
JAK2 inhibitor G5-7 (JAK2 inhibitor G5-7) is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for glioma study
价 格：￥电议型 号：T8742产 地：中国大陆
-
T8661AS601245.2TFA (345987-15-7 free base)；化合物AS601245.2TFAAS601245.2TFA；AS601245.2TFA
AS601245.2TFA (345987-15-7 free base) (AS601245.2TFA) is a cell-permeable Inhibitor of JNK (IC50s of 150, 220, and 70 nM for hJNK1, hJNK2, and hJNK3, respectively).
价 格：￥电议型 号：T8661产 地：中国大陆
-
T76366CART (55-76), rat；化合物 CART (55-76), ratCART (55-76), rat
CART (55-76), rat, a neuropeptide comprising residues 55-76 of the CART peptide and serving as the N-terminal fragments of CART (55-102), functions as a rat satiety factor. It demonstrates potent appetite-suppressing activity and has a close association with leptin and neuropeptide Y. Additionally, CART (55-76), rat is known to induce anxiety and stress-related behavior [1].
价 格：￥电议型 号：T76366产 地：中国大陆
-
T6139LA-674563 2HCl(552325-73-2(fb-2hcl))；化合物A-674563 2HClA-674563 2HCl(552325-73-2(fb-2hcl))
A-674563 2HCl is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.
价 格：￥电议型 号：T6139L产 地：中国大陆
-
T4690Betrixaban hydrochloride(330942-05-7(free base))；盐酸贝曲西班PRT054021 hydrochloride；PRT054021 hydrochlori
Betrixaban hydrochloride(330942-05-7(free base)) (PRT054021 hydrochloride) is a potent, selective, and orally efficacious factor Xa (fXa) inhibitor (IC50: 1.5 nM).
价 格：￥电议型 号：T4690产 地：中国大陆
-
T4444A-674563 HCl (552325-73-2(free base))；化合物A-674563 HClA-674563 HCl (552325-73-2(free base))
A-674563 is an orally available, ATP-competitive, and reversible inhibitor of Akt (Ki: 11 nM for Akt1) [1]. It exhibits inhibitory activity against PKA and Cdk2 (IC50: 16/46 nM) but is 10- to >1, 800-fold selective for Akt1 versus additional kinases in the CMGC, CAMK, and TK families [1].
价 格：￥电议型 号：T4444产 地：中国大陆
-
T40379Bax BH3 peptide (55-74), wild type；Bax BH3 peptide (55-74), wild typeBax BH3 peptide (55-74), wild t
Bax BH3 peptide (55-74), wild type is a 20-amino acid peptide (Bax 1) known for its ability to induce apoptosis in various cell line models.
价 格：￥电议型 号：T40379产 地：中国大陆
-
T31268Deanol pidolate；化合物 T31268EINECS 245-706-1；EINECS 245-706-1
Deanol pidolate is a biochemical.
价 格：￥电议型 号：T31268产 地：中国大陆
-
T30188L1(Iso)-Atagabalin HCl；异构体Atagabalin盐酸盐(Iso)-Atagabalin HCl((Iso)-223445-75-8)；(Iso)-Atagabalin HCl((I
(Iso)-Atagabalin HCl(isomer-Atagabalin HCl) is an alpha -2- delta ligand that can be used to treat non-restorative sleep.
价 格：￥电议型 号：T30188L1产 地：中国大陆
