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
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:3869725
已选条件
-
TP1087Substance PNK receptor,Neurokinin Receptor,Endogenous Metabolite,Substance P,inhibit,Tachykinin rece
Substance P (SP) is an undecapeptide (a peptide composed of a chain of 11 amino acid residues) member of the tachykinin neuropeptide family.
价 格:¥电议型 号:TP1087产 地:中国大陆
-
T6816DASA-58DASA58,inhibit,Inhibitor,DASA 58,DASA-58,glycolysis,TXNIP,cancer metabolism,Pyruvate Kinase,p
DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.
价 格:¥电议型 号:T6816产 地:中国大陆
-
TN7138Methyl 5-hydroxy-1H-indole-3-carboxylate
Methyl 5-hydroxy-1H-indole-3-carboxylate is a marine derived natural products found in Hyrtios erectus.
价 格:¥电议型 号:TN7138产 地:中国大陆
-
T7752(S,R,S)-AHPC-MeVHL ligand-2,VHL ligand2,Inhibitor,inhibit,Ligands for E3 Ligase,(S,R,S) AHPC Me,(S,R
(S,R,S)-AHPC-Me (VHL ligand 2) is the (S,R,S)-AHPC-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein[1]. (S,R,S)-AHPC-Me can be used to synthesize ARV-771. ARV-771 is a von Hippel-Landau (VHL) E3 ligase-based BET PROTAC degrader. ARV-771 potently degrades BET protein in castration-resistant prostate cancer (CRPC) cells with a DC50 <1 nM.
价 格:¥电议型 号:T7752产 地:中国大陆
-
TN1032Geissoschizine methyl ether5-HT Receptor,Geissoschizine methyl ether,Inhibitor,inhibit,5-hydroxytryp
Geissoschizine methyl ether, a major indole alkaloid found in Uncaria hook, is a major active component of Yokukansan with psychotropic effects. Geissoschizine methyl ether is a potent serotonin A receptor agonist and candidate for amelioration of aggressiveness and sociality by yokukansan
价 格:¥电议型 号:TN1032产 地:中国大陆
-
T40515MetamitronInhibitor,Metamitron,inhibit
Metamitron is a photosynthetic electron transport chain inhibitor and can be used as a chemical thinner.
价 格:¥电议型 号:T40515产 地:中国大陆
-
T6926PalmitoylethanolamideEndogenous Metabolite,inhibit,Loramine P256,Palmitoylethanolamide,Inhibitor,Lor
Palmitoylethanolamide(PEA) , an endogenous fatty acid amide, activates PPAR-α selectively in vitro (EC50=3.1±0.4 μM).
价 格:¥电议型 号:T6926产 地:中国大陆
-
TP1426His-[D-2-ME-Trp]-AlaHis[D2METrp]Ala,His [D 2 ME Trp] Ala
His-[D-2-ME-Trp]-Ala is a peptide fragment of the growth hormone hexarelin.
价 格:¥电议型 号:TP1426产 地:中国大陆
-
TQ0094JNJ-40411813ADX71149,JNJ-40411813,ADX 71149,JNJ40411813,mGluR,Inhibitor,JNJ 40411813,Metabotropic gl
JNJ-40411813 (ADX-71149) is a new positive allosteric modulator of the metabotropic glutamate 2 receptor (mGlu2R, EC50: 147 nM).
价 格:¥电议型 号:TQ0094产 地:中国大陆
-
T8753LX-2761 intermediateLX 2761 intermediate,LX2761 intermediate
LX-2761 intermediate a chemical compound.
价 格:¥电议型 号:T8753产 地:中国大陆
-
T76216-?ThioinosineNucleoside Antimetabolite/Analog,6 ?Thioinosine,6-?Thioinosine,inhibit,Inhibitor,6?Thi
6- Thioinosine (6TI) is a purine antimetabolite, acts as an anti-adipogenesis agent.
价 格:¥电议型 号:T7621产 地:中国大陆
-
T16040Mepazinediffuse,B cell,inhibit,large,mucosa associated lymphoid tissue lymphoma translocation gene 1
Mepazine is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM. Mepazine enhances apoptosis and affects the cell viability.
价 格:¥电议型 号:T16040产 地:中国大陆
-
T6636RefametinibMEK1,allosteric,RDEA 119,BAY-869766,inhibit,Inhibitor,MAP2K,MEK2,orally,MAPKK,RDEA-119,Mi
Refametinib (RDEA119, Bay 86-9766) is an effective, ATP non-competitive and specific inhibitor of MEK1/2 (IC50: 19/47 nM).
价 格:¥电议型 号:T6636产 地:中国大陆
-
T8929BC1618Ubiquitin activating enzyme,Mitochondrial Autophagy,fission,Mitophagy,inhibit,Inhibitor,mTORC,
BC1618 is an orally active Fbxo48 inhibitory compound, stimulates Ampk-dependent signaling. It promotes mitochondrial fission, facilitates autophagy and improves hepatic insulin sensitivity.
价 格:¥电议型 号:T8929产 地:中国大陆
-
TN1918Medicarpininhibit,Inhibitor,Apoptosis,Medicarpin
Medicarpin, a legume phytoalexin, acts as an estrogen receptor (ER) agonist, can stimulate osteoblast differentiation likely via ERα2, promote achievement of peak bone mass, and is devoid of uterine estrogenicity; in addition, given its excellent oral bioavailability, it can be potential osteogenic agent.
价 格:¥电议型 号:TN1918产 地:中国大陆
-
T80387-Ethoxy-4-Methylcoumarincoumarin,CYPs,inhibit,Inhibitor,P450 2B6,P450 2B4,7Ethoxy4Methylcoumarin,7
7-Ethoxy-4-Methylcoumarin is a natural organic compound
价 格:¥电议型 号:T8038产 地:中国大陆
-
TN71361,7-dimethyl-1H-indole-3-carbaldehyde
1,7-dimethyl-1H-indole-3-carbaldehyde is a marine derived natural products found in Lyngbya majuscula.
价 格:¥电议型 号:TN7136产 地:中国大陆
-
T75481-Methylguanosine1-Methylguanosine,1 Methylguanosine,Endogenous Metabolite,Inhibitor,inhibit,1Methyl
1-Methylguanosine is a methylated nucleoside. It is known that some modified, especially methylated, nucleosides originating from RNA degradation are excreted in abnormal levels in the urine of patients with malignant tumors.
价 格:¥电议型 号:T7548产 地:中国大陆
-
T8405Vardenafil hydrochloridePDE-5 inhibitors,Vardenafil,Endogenous Metabolite,diabetes,Zucker diabetic f
Vardenafil hydrochloride is a New Phosphodiesterase Type 5(PDE5) Inhibitor, in the Treatment of Erectile Dysfunction in Men With Diabetes
价 格:¥电议型 号:T8405产 地:中国大陆
-
T7187Genz-644282Genz 644282,Inhibitor,inhibit,Genz-644282,Topoisomerase
Genz-644282, a novel non-camptothecin topoisomerase I inhibitor for cancer treatment.
价 格:¥电议型 号:T7187产 地:中国大陆