微信关注
China
Total item
Cart Subtotal
￥ 0.00 “betaine hydrochloride”的搜索结果
-
Ciprofloxacin HCl
Catalog No. A16969 Ciprofloxacin hydrochloride是一种广谱抗菌剂羧基氟喹啉，一种广泛用作抗菌剂和免疫调节剂的氟喹诺酮类抗生素。 了解更多 -
Lomerizine dihydrochloride
Catalog No. A16599 -
Anlotinib HCl
Catalog No. A17076 -
HA-100 (C1)
Catalog No. A17019 PKs 抑制剂HA-100 dihydrochloride是具有添加的哌嗪基磺酰基的异喹啉化合物，可充当蛋白激酶（PKs）的抑制剂，包括PKA，PKC和PKG（IC50分别为8、12和4 μM）。 了解更多 -
GR 144053 trihydrochloride
Catalog No. A17198 GR 144053 trihydrochloride是一种有效的选择性血小板纤维蛋白原受体糖蛋白IIb/IIIa（GpIIb/IIIa）拮抗剂。 了解更多 -
Levocetirizine Dihydrochloride
Catalog No. A17440 L-isomer of cetirizine and histamine H1 receptor antagonistLevocetirizine dihydrochloride is a L-isomer of cetirizine and histamine H1 receptor antagonist. It incrases levels of CD4+ CD25+ T cells and decreases levels of eosinophils, decreasing allergy symptoms. 了解更多 -
Tilorone dihydrochloride
Catalog No. A17487 interferon inducerTilorone Dihydrochloride is an antiviral, antineoplastic, and anti-inflammatory agent; Orally active interferon inducer, inhibiting Ebola virus (EBOV). 了解更多 -
Minaprine dihydrochloride
Catalog No. A17722 MAO-A inhibitorMinaprine is a reversible inhibitor of MAO-A; weakly inhibit acetylcholinesterase; an antidepressant for treatment of depression. 了解更多 -
delta-Valerobetaine
Catalog No. A18793 delta-Valerobetaine is a precursor of trimethylamine N-oxide (TMAO). 了解更多 -
Pirenzepine dihydrochloride
Catalog No. A17916 M1 muscarinic receptor antagonistPirenzepine dihydrochloride (LS519) is a selective M1 muscarinic receptor antagonist. 了解更多 -
L-NIO dihydrochloride
Catalog No. A13027 NOS inhibitorL-NIO dihydrochloride is a potent, non-selective and NADPH-dependent nitric oxide synthase (NOS) inhibitor. 了解更多 -
Ranolazine dihydrochloride
Catalog No. A10781 Ranolazine dihydrochloride (CVT 303 dihydrochloride) is an anti-angina drug that achieves its effects by inhibiting the late phase of inward sodium current (INa and IKr with IC50 values of 6 μM and 12 μM, respectively) without affecting heart rate or blood pressure (BP). 了解更多 -
AQ-13 dihydrochloride
Catalog No. A12178 AQ-13 dihydrochloride is an aminoquinoline antimalarial drug that is effective against chloroquine-resistant strains of Plasmodium falciparum. 了解更多 -
Lesopitron dihydrochloride
Catalog No. A12950 5-HT1A receptor agonistLesopitron dihydrochloride is a full and selective 5-HT1A receptor agonist with IC50 of 125 nM in rat hippocampal membranes. 了解更多 -
Canertinib dihydrochloride
Catalog No. A11344 EGFR inhibitorCanertinib dihydrochloride (CI-1033 dihydrochloride) is a potent and irreversible EGFR inhibitor; inhibits cellular EGFR and ErbB2 autophosphorylation with IC50s of 7.4 and 9 nM. 了解更多 -
JDTic dihydrochloride
Catalog No. A11469 KOR antagonistJDTic (dihydrochloride) is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception. 了解更多 -
Y-33075 dihydrochloride
Catalog No. A11611 ROCK inhibitorY-33075 dihydrochloride is a selective ROCK inhibitor with an IC50 of 3.6 nM. 了解更多 -
Mirodenafil dihydrochloride
Catalog No. A18047 PDE-5 inhibitorMirodenafil dihydrochloride (SK3530 dihydrochloride) is a phosphodiesterase type 5 (PDE-5) inhibitor developed for the treatment of erectile dysfunction. 了解更多 -
GW791343 trihydrochloride
Catalog No. A21204 P2X7 allosteric modulatorGW791343 3Hcl is a P2X7 allosteric modulator; exhibits species-specific activity and acts as a negative allosteric modulator of human P2X7 (pIC50 = 6.9 - 7.2). 了解更多 -
SB-277011 dihydrochloride
Catalog No. A21353 dopamine D3 receptor antagonistSB-277011 dihydrochloride (SB-277011A dihydrochloride) is a potent, selective, orally bioavailable and brain penetrate dopamine D3 receptor antagonist, with pKis of 8.0, 6.0, <5.2 and 5.9 for D3, D2, 5-HT1B, and 5-HT1D receptors, respectively. 了解更多 -
Foliglurax monohydrochloride
Catalog No. A21384 glutamate receptor 4 modulatorFoliglurax monohydrochloride (PXT002331 monohydrochloride) is a highly selective and potent, brain-penetrant metabotropic glutamate receptor 4 positive allosteric modulator (mGluR4 PAM) , with an EC50 of 79 nM. Antiparkinsonian effect. 了解更多 -
PF429242 dihydrochloride
Catalog No. A21386 S1P inhibitorPF429242 dihydrochloride is a reversible and competitive S1P inhibitor with an IC50 of 175 nM. 了解更多 -
NVP-BSK805 dihydrochloride
Catalog No. A21406 JAK2 inhibitorNVP-BSK805 dihydrochloride (BSK805 dihydrochloride) is an ATP-competitive JAK2 inhibitor, with IC50s of 0.48 nM, 31.63 nM, 18.68 nM, and 10.76 nM for JAK2 JH1 (JAK homology 1), JAK1 JH1, JAK3 JH1, and TYK2 JH1, respectively. 了解更多 -
CHIR-99021 monohydrochloride
Catalog No. A21430 GSK-3α/β inhibitorCHIR-99021 monohydrochloride (CT99021 monohydrochloride) is a GSK-3α/β inhibitor with IC50 of 10 nM/6.7 nM; > 500-fold selectivity for GSK-3 versus its closest homologs CDC2 and ERK2, as well as other protein kinases. 了解更多 -
CHIR-99021 trihydrochloride
Catalog No. A21436 GSK-3α/β inhibitorCHIR-99021 trihydrochloride (CT99021 trihydrochloride) is a GSK-3α/β inhibitor with IC50 of 10 nM/6.7 nM. 了解更多 -
Naspm trihydrochloride
Catalog No. A21437 CP-AMPA receptors antagonistNaspm trihydrochloride (1-Naphthylacetyl spermine trihydrochloride), a synthetic analogue of Joro spider toxin, is a calcium permeable AMPA (CP-AMPA) receptors antagonist. 了解更多 -
JNJ-37822681 dihydrochloride
Catalog No. A21470 dopamine D2 receptor antagonistJNJ-37822681 dihydrochloride is a potent, specific, centrally active, fast-dissociating dopamine D2 receptor antagonist with a moderate binding affinity for the dopamine D2L receptor (Ki =158 nM), which has potential for the treatment of schizophrenia and bipolar disorder. 了解更多 -
Vofopitant dihydrochloride
Catalog No. A21543 NK1 receptor antagonistVofopitant dihydrochloride (GR 205171A) is a potent, selective and orally available tachykinin neurokinin 1(NK1) receptor antagonist. 了解更多 -
Gusperimus trihydrochloride
Catalog No. A21551 Gusperimus trihydrochloride (Spanidin) is a derivative of the antitumor antibiotic spergualin with immunosuppressant activity. 了解更多 -
GDC-0575 dihydrochloride
Catalog No. A21567 CHK1 inhibitorGDC-0575 dihydrochloride (ARRY-575 dihydrochloride) is an orally bioavailable CHK1 inhibitor, with an IC50 of 1.2 nM, and has antitumor activity. 了解更多 -
Lerociclib dihydrochloride
Catalog No. A21577 CDK4/CDK6 inhibitorLerociclib dihydrochloride (G1T38 dihydrochloride) is a potent and selective inhibitor of CDK4/CDK6, with IC50s of 1 nM and 2 nM for CDK4/CyclinD1 and CDK6/CyclinD3, respectively. 了解更多 -
l-Atabrine dihydrochloride
Catalog No. A21646 l-Atabrine dihydrochloride is a less active enantiomer of quinacrine which displays antiprion activity. 了解更多 -
MRT68921 dihydrochloride
Catalog No. A21650 ULK1/ULK2 inhibitorMRT68921 dihydrochloride is the most potent inhibitor of ULK1 and ULK2, with IC50 values of 2.9 nM and 1.1 nM, respectively. 了解更多 -
LCL521 dihydrochloride
Catalog No. A21656 ACDase inhibitorLCL521 dihydrochloride (1,3DMG-B13 dihydrochloride) is an acid ceramidase (ACDase) inhibitor. 了解更多 -
diABZI STING agonist-1 trihydrochloride
Catalog No. A21694 STING receptor agonistdiABZI STING agonist-1 (trihydrochloride) is a selective stimulator of interferon genes (STING) receptor agonist, with an EC50s of 130 for human PBMCs. 了解更多 -
TLR7/8 agonist 1 dihydrochloride
Catalog No. A21700 TLR7/8 agonistTLR7/8 agonist 1 dihydrochloride is a toll-like receptor (TLR7)/TLR8 dual-agonistic imidazoquinoline. 了解更多 -
Lys01 trihydrochloride
Catalog No. A21702 lysosomal autophagy inhibitorLys01 trihydrochloride (Lys05) is a novel lysosomal autophagy inhibitor with IC50 values of 3.6, 3.8, 6 and 7.9 μM for 1205Lu, c8161, LN229 and HT-29 cell line in the MTT assay. 了解更多 -
N8-Acetylspermidine dihydrochloride
Catalog No. A21720 N8-Acetylspermidine dihydrochloride is a polyamine. 了解更多 -
MCOPPB triHydrochloride
Catalog No. A21722 nociceptin receptor agonistMCOPPB 3Hcl is a nociceptin receptor agonist with pKi of 10.07; weaker activity at other opioid receptors. 了解更多 -
GSK3368715 dihydrochloride
Catalog No. A21733 PRMT inhibitorGSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50=3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)). 了解更多 -
Ipatasertib dihydrochloride
Catalog No. A21734 pan-Akt inhibitorIpatasertib dihydrochloride (GDC-0068 dihydrochloride) is a highly selective pan-Akt inhibitor targeting Akt1/2/3 with IC50 of 5/18/8 nM, 620-fold selectivity over PKA. 了解更多 -
Philanthotoxin 74 dihydrochloride
Catalog No. A21739 AMPAR antagonistPhilanthotoxin 74 dihydrochloride (PhTx 74) is an AMPAR antagonist; inhibits GluR3 and GluR1 with IC50s of 263 and 296 nM, respectively. 了解更多 -
K-604 dihydrochloride
Catalog No. A21773 ACAT-1 inhibitorK-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 (ACAT-1) inhibitor with an IC50 of 0.45??0.06 μM. 了解更多 -
Lexibulin dihydrochloride
Catalog No. A21774 tubulin polymerisation inhibitorLexibulin 2Hcl (CYT-997 2Hcl) is a potent tubulin polymerisation inhibitor with IC50 of 10-100 nM in cancer cell lines; with potent cytotoxic and vascular disrupting activity in vitro and in vivo. 了解更多 -
DDR1-IN-1 dihydrochloride
Catalog No. A21813 DDR1 receptor tyrosine kinase inhibitorDDR1-IN-1 dihydrochloride is a potent and selective DDR1 receptor tyrosine kinase inhibitor with an IC50 of 105 nM; 4-fold less potent for DDR2 (IC50 = 413 nM). 了解更多 -
GSK-LSD1 dihydrochloride
Catalog No. A21815 LSD1 inhibitorGSK-LSD1 dihydrochloride is a potent, selective and irreversible lysine specific demethylase 1 (LSD1) inhibitor with an IC50 of 16 nM. 了解更多 -
B-Raf inhibitor 1 dihydrochloride
Catalog No. A21834 Raf kinase inhibitorB-Raf inhibitor 1 dihydrochloride is a potent Raf kinase inhibitor with Kis of 1 nM, 1 nM, and 0.3 nM for B-RafWT, B-RafV600E, and C-Raf, respectively. 了解更多 -
Liarozole dihydrochloride
Catalog No. A21853 CYP450 dependent inhibitorLiarozole dihydrochloride (R75251; R85246) is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase). 了解更多 -
MW-150 dihydrochloride dihydrate
Catalog No. A21860 p38α MAPK inhibitorMW-150 dihydrochloride dihydrate (MW01-18-150SRM dihydrochloride dihydrate) is a selective, CNS penetrant, and orally active inhibitor of p38α MAPK with a Ki of 101 nM. 了解更多
联系我们
United StatesAdooq Bioscience
Toll Free: (866) 930-6790
Fax: +1-323-606-8156
Email: sales@adooq.com
Not your Region? View all Distributors
最近查看过的产品
FILTER BY:
购物选项
- 分类
-
- Epigenetics (16)
- Apoptosis (7)
- PI3K / Akt / mTOR (13)
- Protein Tyrosine Kinases (20)
- Angiogenesis (23)
- MAPK (11)
- JAK / Stat (9)
- Cell Cycle (14)
- DNA Damage (19)
- Cytoskeleton (2)
- Cell Metabolism (28)
- Autophagy Signaling (4)
- Immunology & Inflammation (8)
- GPCR / G Protein (145)
- NF-kB/IkB (3)
- TGF-β / Smad (10)
- Neuronal Signaling (34)
- Proteases (8)
- Microbiology (5)
- Stem Cells / Wnt (4)
- Membrane Transporters/Ion Channels (27)
- Endocrinology / Hormones (8)
- PROTACs (3)
- Others (32)
- Natural Products (12)
- Ready to Use Solution (55)
- Products On Sale (77)
- Monoclonal Antibodies (1)
- Enzymes (2)
- COVID-19 Related Products (3)
- 作用机制
-
- Inhibitor (抑制剂) (211)
- Agonist (激动剂) (67)
- Antagonist (拮抗剂) (85)
- Activator (激活剂) (7)
- Modulator (调节剂) (7)
- Blocker (阻断剂) (18)
- Inducer (诱导剂) (2)
- Stabilizer (稳定剂) (3)
- 靶点
-
- A1 adenosine receptor (1)
- B-Raf (2)
- Bcl-xL (1)
- C-Raf (Raf-1) (2)
- COX-1 (1)
- COX-2 (1)
- CXCR4 (1)
- DNA-PK (1)
- EGFR (2)
- EGFR L858R (1)
- EGFR L861Q (1)
- EGFR T790M (1)
- HDAC1 (1)
- HDAC3 (1)
- HDAC6 (1)
- HDAC8 (1)
- Histamine H1 receptor (1)
- JAK2 (1)
- KDM1A (LSD1) (1)
- L3MBTL1 (1)
- Lck (1)
- MAO-A (1)
- MAO-B (1)
- p110α (1)
- p110β (1)
- p110γ (1)
- p110δ (1)
- p53 (3)
- PARP (1)
- PDGFRβ (1)
- Pim1 (1)
- Pim2 (1)
- Pim3 (1)
- PRMT5 (1)
ADOOQ 产品质量保证
We promise all products to perform as described.