Signaling Pathways(信号通路)
- Proteases(4106)
- Apoptosis(2733)
- Chromatin/Epigenetics(1612)
- Metabolism(3106)
- MAPK Signaling(575)
- Tyrosine Kinase(1406)
- DNA Damage/DNA Repair(1791)
- PI3K/Akt/mTOR Signaling(648)
- Microbiology & Virology(3522)
- Cell Cycle/Checkpoint(1381)
- Ubiquitination/ Proteasome(1293)
- JAK/STAT Signaling(546)
- TGF-β / Smad Signaling(360)
- Angiogenesis(354)
- GPCR/G protein(3387)
- Stem Cell(458)
- Membrane Transporter/Ion Channel(2267)
- Cancer Biology(685)
- Endocrinology and Hormones(949)
- Neuroscience(3961)
- Obesity, Appetite Control & Diabetes(357)
- Other Signal Transduction(122)
- Immunology/Inflammation(4267)
- Cardiovascular(866)
- Vitamin D Related(72)
- Antibody-drug Conjugate/ADC Related(845)
- PROTAC(250)
- Ox Stress Reagents(513)
- Others(1704)
- Antiparasitics(147)
- Toxins(87)
- Cat.No. 产品名称 Information
-
GC52100
(Arg)9 (trifluoroacetate salt)
Nona-Arginine, Poly-Arginine-9, RRRRRRRRR
A cationic cell-penetrating peptide -
GC12395
(D)-(+)-Neopterin
新蝶呤,D-(+)-Neopterin; D-erythro-Neopterin
A biochemical tool to screen for immune disorders -
GC50482
(D)-PPA 1
An inhibitor of the PD-1-PD-L1 protein-protein interaction
-
GC52442
(D)-PPA 1 (trifluoroacetate salt)
DPPA-1, NYSKPTDRQYHF
An inhibitor of the PD-1-PD-L1 protein-protein interaction -
GC69009
(D)-PPA 1 TFA
(D)-PPA 1 TFA 是一种抗水解 D 肽拮抗剂。(D)-PPA 1 TFA 是一种有效的 PD-1/PD-L1 抑制剂。(D)-PPA 1 TFA 与 PD-1 结合的亲和力为 0.51 μM,体内外均有效。
-
GC41698
(D)2-Rh 110 (trifluoroacetate salt)
D2R, (Asp)2-Rhodamine 110, Rhodamine 110 bis-(L-aspartic acid amide)
A fluorogenic caspase substrate -
GA20063
(D-Ala²)-Gastric Inhibitory Polypeptide (human)
D-ALA2]-GIP(HUMAN)-胃抑素
GIP receptor agonist. -
GA20156
(D-Ser(tBu)⁶,Azagly¹⁰)-LHRH (free base)
戈舍瑞林; ICI 118630
-
GC41699
(Des-octanoyl)-Ghrelin (human) (trifluoroacetate salt)
A peptide hormone
-
GC60399
(E)-10-Hydroxynortriptyline
E-10-OH-NT
An active metabolite of amitriptyline and nortriptyline -
GC41700
(E)-2-(2-Chlorostyryl)-3,5,6-trimethylpyrazine
CSTMP
A stilbene derivative with antioxidant and anticancer activities -
GC15373
(E)-2-Decenoic acid
反式-2-癸烯酸,trans-2-Decenoic acid
An unsaturated fatty acid found in royal jelly -
GC41268
(E)-2-Hexadecenal
trans-2-Hexadecenal
A long-chain fatty aldehyde -
GC41701
(E)-2-Hexadecenal Alkyne
A click chemistry probe for a sphingolipid degradation product
-
GC66255
(E)-3,4,5-Trimethoxycinnamic acid
TMCA
(E)-3,4,5-Trimethoxycinnamic acid (TMCA) 是一种被多甲氧基取代的肉桂酸。(E)-3,4,5-Trimethoxycinnamic acid 是一种口服有效的 GABAA/BZ 受体激动剂。(E)-3,4,5-Trimethoxycinnamic acid 与 5-HT2C 和 5-HT1A 受体具有良好的结合亲和力,其 IC50 值分别为 2.5 和 7.6 μM。(E)-3,4,5-Trimethoxycinnamic acid 具有抗惊厥和镇静活性。(E)-3,4,5-Trimethoxycinnamic acid 可用于失眠、头痛、癫痫的研究。 -
GC65239
(E)-3,4-(Methylenedioxy)cinnamic acid
(2E)-3-(1,3-苯并二氧杂环戊-5-基)-2-丙烯酸,(E)-Piperonylprop-2-enoic acid
(E)-3,4-(Methylenedioxy)cinnamic acid 是从Brombya platynema的茎皮中获得的肉桂酸衍生物。 -
GC72618
(E)-3,4-Dimethoxychalcone
(E)-3,4-Dimethoxychalcone是3,4-二甲氧基查尔酮的同工型,是一种潜在的抗菌剂和抗氧化剂。
-
GC61668
(E)-3,4-Dimethoxycinnamic acid
(E)-3,4-二甲氧基肉桂酸; (E)-O-Methylferulic acid
(E)-3,4-Dimethoxycinnamicacid是3,4-Dimethoxycinnamicacid的低活性异构体。3,4-Dimethoxycinnamicacid是从Securidacainappendiculata中提取和纯化的单体。3,4-Dimethoxycinnamicacid通过ROS介导的信号途径对L-02细胞发挥抗凋亡作用。 -
GC34978
(E)-4-Hydroxytamoxifen
(E)-4-羟基他莫昔芬; (E)-Afimoxifene
(E)-4-Hydroxytamoxifen 是 (Z)-4-hydroxytamoxifen 的低活性异构体,是雌激素受体 (estrogen receptor) 调节剂。 -
GC41702
(E)-5-(2-Bromovinyl)uracil
(E)-5-(2-溴乙烯基)-2-脱氧尿苷
A pyrimidine base -
GC40295
(E)-8-Methyl-6-nonenoic Acid
(E)-8-甲基-6-壬烯酸
A potential thermal degradant of capsaicin -
GC34125
(E)-[6]-Dehydroparadol
(E)-[6]-Dehydroparadol来自专利US9272994化合物M15,能够抑制人体癌细胞生长并且诱导细胞凋亡。在HCT-116和H-1299细胞中的IC50值分别为43.02和41.59μM。
-
GC49003
(E)-Ajoene
NSC 614554
A disulfide with diverse biological activities -
GC62122
(E)-Akt inhibitor-IV
(E)-AKTIV
(E)-Akt inhibitor-IV is a PI3K-Akt inhibitor, with potent cytotoxic. -
GC32522
(E)-Alprenoxime (CDDD-1815)
CDDD-1815
(E)-Alprenoxime (CDDD-1815) 是 Alprenoxime 的异构体。 -
GC41703
(E)-C-HDMAPP (ammonium salt)
(E)5hydroxy4methylpent3enyl pyrophosphate
Activator of γδ-T-lymphocytes -
GC62733
(E)-Coniferin
松柏苷,(E)-Laricin
(E)-Coniferin 是Coniferin 的一种异构体。Coniferin (Laricin) 是松柏醇的一种葡萄糖苷。Coniferin 抑制真菌生长和黑化反应。 -
GC70220
(E)-Crotylbarbital
(E)-Crotylbarbital是巴比妥的异构体。
-
GC17800
(E)-FeCP-oxindole
VEGFR-2 inhibitor
-
GC46335
(E)-Fenpyroximate
唑螨酯
A phenoxypyrazole acaricide -
GC34980
(E)-Ferulic acid
反式阿魏酸,(E)-Coniferic acid
Trans-ferulic acid is a potent activator of AMPKunder high glucose condition. -
GC66371
(E)-Ferulic acid-d3
(E)-Coniferic acid-d3
(E)-Ferulic acid-d3 ((E)-Coniferic acid-d3) 是 (E)-Ferulic acid 的氘代物。(E)-Ferulic acid 是阿魏酸 (Ferulic acid) 的异构体,阿魏酸是芳香族化合物,在植物细胞壁中丰富。 (E)-Ferulic acid 引起 β-连环蛋白 (β-catenin) 的磷酸化,导致蛋白酶体降解,增加促凋亡因子 Bax 的表达并降低促存活因子存活蛋白的表达。(E)-Ferulic acid 可以有效去除活性氧 (ROS) 和抑制脂质过氧化。(E)-Ferulic acid 在人肺癌细胞系 H1299 中发挥抗增殖和抗迁移作用。 -
GC34981
(E)-Flavokawain A
卡瓦胡椒素A
A chalcone with diverse biological activities -
GC46336
(E)-Guggulsterone
孕二烯二酮,(E)-Guggulsterone
A farnesoid X receptor antagonist -
GC91418
(E)-KPT-330
KTP-330; trans Selinexor
(E)-KPT-330是selinexor的代谢产物,它是exportin 1 (XPO1/CRM1)抑制剂的一种。它由细胞色素P450(CYP)亚型CYP3A4从selinexor中形成。 -
GC34982
(E)-LHF-535
(E)-LHF-535 是 LHF-535 的异构体. LHF-535 是一种抗病毒剂,对 Lassa,Machupo,Junin,VSVg 病毒的 EC50 分别为 <1 μM,<1 μM,<1 μM 和 1-10 μM,详细信息请参考专利文献 WO2012006552A1 中的化合物 1。
-
GC38684
(E)-m-Coumaric acid
3-羟基肉桂酸
3-hydroxycinnamic acid (meta-Coumaric acid, m-Coumaric acid, m-Coumarate) is an aromatic acid that can be found in vinegar. -
GC61437
(E)-Methyl 4-coumarate
4-羟基肉桂酸甲酯; Methyl trans-p-coumarate
A phenol with diverse biological activities -
GC62734
(E)-Oct-2-enoic acid
2-辛烯酸
2-Octenoic acid (2-Octenoate) is a normal organic acid produced by hepatic microsomal oxidation of aliphatic aldehydes and is a metabolite naturally found in the urine and plasma. -
GC63903
(E)-Osmundacetone
(E)-紫萁酮
(E)-Osmundacetone 是 Osmundacetone 的异构体。Osmundacetone 可以显着抑制 MAPK 磷酸化,包括 JNK,ERK 和 p38 激酶,具有抗氧化应激的神经保护作用。 -
GC72591
(E,E)-RGFP966
(E,E)-RGFP966是一种选择性、可穿透中枢神经系统的HDAC3抑制剂,可用于亨廷顿病的研究。
-
GC40286
(E,Z)-2-propyl-2-Pentenoic Acid
2-丙基-2-戊烯酸
A valproic acid metabolite -
GC49189
(E/Z)-4-hydroxy Tamoxifen-d5
Afimoxifene-d5, 4-OHT-d5
An internal standard for the quantification of (E/Z)-4-hydroxy tamoxifen -
GC61807
(E/Z)-AG490
酪氨酸磷酸化抑制剂AG490,(E/Z)-Tyrphostin AG490; (E/Z)-Tyrphostin B42
(E/Z)-AG490((E/Z)-TyrphostinAG490)是(E)-AG490和(Z)-AG490的消旋体。(E)-AG490是一种酪氨酸激酶抑制剂,可抑制EGFR,Stat-3和JAK2/3。
-
GC25000
(E/Z)-BCI
BCI, NSC 150117
(E/Z)-BCI (BCI, NSC 150117) is an inhibitor of dual specific phosphatase 1/6 (DUSP1/DUSP6) and mitogen-activated protein kinase with EC50 of 13.3 μM and 8.0 μM for DUSP6 and DUSP1 in cells, respectively. (E)-BCI induces apoptosis via generation of reactive oxygen species (ROS) and activation of intrinsic mitochondrial pathway in H1299 lung cancer cells. -
GC91543
(E/Z)-Droloxifene
3-Hydroxytamoxifen
(E/Z)-Droloxifene is a mixture of (E)-droloxifene, a selective estrogen receptor modulator (SERM), and (Z)-droloxifene. -
GC62407
(E/Z)-Eltrombopag 13C
(E/Z)-SB-497115 13C4
(E/Z)-Eltrombopag 13C ((E/Z)-SB-497115 13C4) 是 E-Eltrombopag 和 Z-Eltrombopag 的混合复合物,带有 13C 标记。 -
GC40833
(E/Z)-Endoxifen
N-去甲基-4-羟基-
An active metabolite of tamoxifen -
GC62735
(E/Z)-GO289
(E/Z)-GO289 potently and selectively inhibits casein kinase 2 (CK2) at an IC50 of 7 nM in vitro kinase assay.
-
GC62736
(E/Z)-GSK-3β inhibitor 1
(E/Z)-GSK-3β inhibitor 1 is a racemic compound of (E)-GSK-3β inhibitor 1 and (Z)-GSK-3β inhibitor 1 isomers, in which GSK-3β inhibitor 1 (compound 3a) is a glycogen synthase kinase 3β (GSK-3β) inhibitor with an IC50 of 4.19 nM.