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T1097Loratadine;氯雷他定SCH 29851|||Loratidine;氯雷他定|||SCH 29851|||Loratidine
Loratadine (SCH 29851) is a second-generation histamine H1 receptor antagonist used in the treatment of allergic rhinitis and urticaria. Unlike most classical antihistamines (HISTAMINE H1 ANTAGONISTS) it lacks central nervous system depressing effects such as drowsiness.
价 格:¥电议型 号:T1097产 地:中国大陆
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T10966DC-5163;化合物 T10966DC-5163
DC-5163 is a potent inhibitor of glyceraldehyde 3-phosphate dehydrogenase (GAPDH) with IC50 of 176.3 nM and Kd of 3.192 μM. DC-5163 selectively inhibits cancer cell proliferation and induces apoptosis, and partially inhibits the glycolysis pathway.
价 格:¥电议型 号:T10966产 地:中国大陆
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T10958Dapagliflozin-d5;化合物 T10958BMS-512148 D5;BMS-512148 D5
Dapagliflozin D5 (BMS-512148 D5) is deuterated Dapagliflozin. Dapagliflozin is a competitive SGLT2 inhibitor.
价 格:¥电议型 号:T10958产 地:中国大陆
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T10952LDabuzalgron HCl;化合物 T10952LR1240|||R-450|||R450|||RO-1151240|||R-1240|||RO1151240;R1240|||R-450|||R4
Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence.
价 格:¥电议型 号:T10952L产 地:中国大陆
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T10951Dabigatran ethyl ester hydrochloride化合物T10951N-[[2-[[[4-(氨基亚氨甲基)苯基]氨基]甲基]-1-甲基-1H-苯并咪唑-5-基]羰基]-N-(2-
Dabigatran ethyl ester hydrochloride is an effective inhibitor of ribosyl dihydronicotinic acid amide dehydrogenase (NQO2) with an IC50 value of 0.8 μM and is a thrombin inhibitor.
价 格:¥电议型 号:T10951产 地:中国大陆
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T10937LD-JNKI-1 acetate;化合物D-JNKI-1 acetateD-JNKI-1 acetate(1445179-97-4 Free base)|||AM-111 acetate;D-JNKI
D-JNKI-1 acetate (AM-111 acetate) is a highly potent and cell-permeable peptide inhibitor of JNK.
价 格:¥电议型 号:T10937L产 地:中国大陆
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T10883CRA-026440;化合物CRA-026440PCI-34051;PCI-34051
CRA-026440(PCI-34051) is a highly potent HDAC inhibitor with inhibitory effects on HDAC1, HDAC2, HDAC3, HDAC6, HDAC8 and HDAC10 with Ki values of 4,14,11,15,7 and 20 nM, respectively. CRA-026440 has anti-tumor and anti-angiogenic activity and can be used to study colon cancer.
价 格:¥电议型 号:T10883产 地:中国大陆
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T10856Cobimetinib (R-enantiomer);考比替尼 (R 型对映体)XL-518 R-enantiomer|||Cobimetinib R-enantiomer|||GDC-0973 R-
Cobimetinib R-enantiomer is the less active R-enantiomer of Cobimetinib which is a selective MEK inhibitor.
价 格:¥电议型 号:T10856产 地:中国大陆
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T10852CNS-5161 hydrochloride;化合物CNS-5161盐酸盐CNS 5161A;CNS 5161A
CNS-5161 hydrochloride (CNS 5161A) is a new antagonist of NMDA ion-channel. It interacts with the NMDA receptor/ion channel site to produce a noncompetitive blockade of the actions of glutamate.
价 格:¥电议型 号:T10852产 地:中国大陆
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T10851CMP-Sialic acid sodium salt;CMP-Sialic acid 钠盐CMP-Neu5Ac sodium salt;CMP-Neu5Ac sodium salt
CMP-Sialic acid sodium salt (CMP-Neu5Ac sodium salt) is a variant inhibitor of UDP-GlcNAc 2-epimerase, the activated form of sialic acid, which is widely found in animals and is involved in the metabolism of organisms.
价 格:¥电议型 号:T10851产 地:中国大陆
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T10751Cefetrizole;头孢三唑Cefetrizole
Ceftezole is an α-Glucosidase inhibitor (IC50: 2.1 μM; Ki: 0.578 μM).
价 格:¥电议型 号:T10751产 地:中国大陆
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T10750Cecropin A TFA (80451-04-3 free base);化合物 T10750Cecropin A TFA;Cecropin A TFA
Cecropin A TFA is an antimicrobial polypeptide isolated from Hyalaphora cecropia pupae with anti-inflammatory, anti-bacterial, and anti-cancer activity.
价 格:¥电议型 号:T10750产 地:中国大陆
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T10695CB1151;化合物 T10695CB1151
CB1151 is a 20-epi analogue of 1,25 dihydroxyvitamin D3 with anti-tumor effects. It inhibits MCF-7 cell growth (IC50: 0.82 nM).
价 格:¥电议型 号:T10695产 地:中国大陆
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T10651c-Kit-IN-3;化合物c-Kit-IN-3c-Kit-IN-3
c-Kit-IN-3 is a selective inhibitor of c-KIT kinase with IC50s of 4 nM and 8 nM for c-Kit (wt) and c-Kit (T670I).
价 格:¥电议型 号:T10651产 地:中国大陆
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T10631Bucindolol布新洛尔BMY 13105|||MJ 131051|||MJ 13105
Bucindolol (BMY 13105) is a novel and potent β1-adrenergic receptor blocker that mediates vasodilation and can be used to study chronic heart failure.
价 格:¥电议型 号:T10631产 地:中国大陆
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T10598BR351 precursor;化合物 T10598BR351 precursor
BR351 precursor is a precursor of BR351. BR351 is a brain penetrant MMP inhibitor (IC50s: 4, 2, 11, 50 nM for MMP2, MMP8, MMP9 and MMP13).
价 格:¥电议型 号:T10598产 地:中国大陆
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T10597BR351;化合物 T10597BR351
BR351 is a brain penetrant MMP inhibitor (IC50s: 4, 2, 11, 50 nM for MMP2, MMP8, MMP9 and MMP13).
价 格:¥电议型 号:T10597产 地:中国大陆
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T10551Bithionol sulfoxide;硫双二氯酚亚砜Bithionol sulfoxide
Bithionol sulfoxide is a clinically approved antiparasitic drug with the inhibitory against solid tumor growth in several preclinical cancer models.
价 格:¥电议型 号:T10551产 地:中国大陆
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T10518BET-BAY 002;化合物 T10518BET-BAY 002
BET-BAY 002 is an effective BET inhibitor and exhibits efficacy in a multiple myeloma model.
价 格:¥电议型 号:T10518产 地:中国大陆
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T10517BET-BAY 002 (S enantiomer);化合物 T10517BET-BAY 002 (S enantiomer)
The S-enantiomer of BET-BAY 002, referred to as BET-BAY 002 S enantiomer, is a potent inhibitor of BET (Bromodomain and Extra-Terminal motif proteins).
价 格:¥电议型 号:T10517产 地:中国大陆