Transcription Factors
Products Related to Transcription Factors(118)
- GC19523Sivelestat sodium tetrahydrateCAS: 201677-61-4Purity: >99.00%
Sivelestat sodium tetrahydrate is a specific inhibitor of neutrophil elastase with an IC 50 value of 14nM.
- GC20007Ginsenoside CKCAS: 39262-14-1Purity: >98.00%
Ginsenoside CK, a secondary ginsenoside biotransformed from major ginsenosides, is more bioavailable and soluble than its parent ginsenosides and holds great significance.
- GC40440(±)8(9)-EETPurity: >98.00%
(±)8(9)-EET is a fully racemic version of the R/S enantiomeric forms biosynthesized from arachidonic acid.
- GC40838(±)8(9)-EET methyl esterPurity: >98.00%
(±)8(9)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450.
- GC420752,4-Pyridinedicarboxylic Acid (hydrate)CAS: 207671-42-9Purity: >98.00%
2,4-Pyridinedicarboxylic Acid (2,4-PDCA) is a compound that structurally mimics 2-oxoglutarate (2-OG, also known as α-ketoglutarate) and chelates zinc, thus affecting a range of enzymes.
- GC42880Avenanthramide-C methyl esterCAS: 955382-52-2Purity: >90.00%
Avenanthramide-C methyl ester is an inhibitor of NF-κB activation that acts by blocking the phosphorylation of IKK and IκB (IC50 ~ 40 μM).
- GC42953BMS 345541 (trifluoroacetate salt)Purity: >98.00%
BMS 345541 is a cell permeable inhibitor of the IκB kinases IKKα and IKKβ (IC50s = 4 and 0.3 μM).
- GC42954BMS 470539 (hydrochloride)CAS: 2341796-82-3Purity: >99.50%
BMS 470539 (hydrochloride) is a highly selective and potent melanocortin-1 receptor (MC-1R) agonist. In cAMP accumulation assays, its EC 50 values for human and mouse MC1R are 16.8 and 11.6nM, respectively.
- GC42997Butyrolactone ICAS: 87414-49-1Purity: >98.00%
بوتيرولاكتون 1 هو مثبط تنافسي لـ ATP لـ CDK1 كمستقلب ثانوي من A. terreusبوتيرولاكتون 1 له تأثيرات مضادة للأورام في الرئة ذات الخلايا غير الصغيرة والرئة ذات الخلايا الصغيرة وخطوط خلايا سرطان البروستاتا
- GC43110C8 Galactosylceramide (d18:1/8:0)CAS: 41613-16-5Purity: >98.00%
C8 Galactosylceramide is a synthetic C8 short-chain derivative of known membrane microdomain-forming sphingolipids.
- GC43212CCG-232601CAS: 1922099-21-5Purity: >98.00%
CCG-232601 (المركب 8f) هو مثبط مسار نسخ Rho / MRTF / SRF فعال وفعال عن طريق الفم
- GC43368D,L-1′-Acetoxychavicol AcetateCAS: 52946-22-2Purity: >95.00%
D,L-1′-Acetoxychavicol acetate is a natural compound first isolated from the rhizomes of ginger-like plants.
- GC43493DL-Sulforaphane N-acetyl-L-cysteineCAS: 334829-66-2Purity: >98.00%
Nrf2 activation of the antioxidant response element (ARE) is central to cytoprotective gene expression against oxidative and/or electrophilic stress.
- GC43894IKK2 Inhibitor VICAS: 354811-10-2Purity: >95.00%
Inhibitor of NF-κB kinase 2 (IKK2, also known as IKKβ) acts as part of an IKK complex in the canonical NF-κB pathway, phosphorylating inhibitors of NF-κB (IκBs) to initiate signaling.
- GC44388NF-κB ControlCAS: 201608-17-5Purity: >95.00%
NF-κB inhibitor is a synthetic peptide corresponding to the nuclear localization sequence (NLS) of NF-κB p105 subunit (also known as p50) appended to a hydrophobic sequence to facilitate import into living cells.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC19069 | BI605906 | 960293-88-3 | - | |
BI605906 is a novel IKKβ inhibitor with an IC50 value of 380 nM when assayed at 0.1 mM ATP. | ||||
| GC19523 | Sivelestat sodium tetrahydrate | 201677-61-4 | >99.00% | |
Sivelestat sodium tetrahydrate is a specific inhibitor of neutrophil elastase with an IC 50 value of 14nM. | ||||
| GC20007 | Ginsenoside CK | 39262-14-1 | >98.00% | |
Ginsenoside CK, a secondary ginsenoside biotransformed from major ginsenosides, is more bioavailable and soluble than its parent ginsenosides and holds great significance. | ||||
| GC40440 | (±)8(9)-EET | - | >98.00% | |
(±)8(9)-EET is a fully racemic version of the R/S enantiomeric forms biosynthesized from arachidonic acid. | ||||
| GC40838 | (±)8(9)-EET methyl ester | - | >98.00% | |
(±)8(9)-EET is biosynthesized in rat and rabbit liver microsomes by CYP450. | ||||
| GC42075 | 2,4-Pyridinedicarboxylic Acid (hydrate) | 207671-42-9 | >98.00% | |
2,4-Pyridinedicarboxylic Acid (2,4-PDCA) is a compound that structurally mimics 2-oxoglutarate (2-OG, also known as α-ketoglutarate) and chelates zinc, thus affecting a range of enzymes. | ||||
| GC42743 | AEM1 | 1030123-90-0 | >98.00% | |
AEM1 هو مثبط Nrf2يقلل AEM1 من تعبيرات الجينات المعتمدة على Nrf2 في خلايا A549 ويمنع نمو خلايا A549 في المختبر وفي الجسم الحي | ||||
| GC42880 | Avenanthramide-C methyl ester | 955382-52-2 | >90.00% | |
Avenanthramide-C methyl ester is an inhibitor of NF-κB activation that acts by blocking the phosphorylation of IKK and IκB (IC50 ~ 40 μM). | ||||
| GC42925 | Berteroin | 4430-42-6 | >95.00% | |
البيرتيروين ، وهو نظير طبيعي للسلفورافين ، وهو عامل مضاد للقسطرة | ||||
| GC42953 | BMS 345541 (trifluoroacetate salt) | - | >98.00% | |
BMS 345541 is a cell permeable inhibitor of the IκB kinases IKKα and IKKβ (IC50s = 4 and 0.3 μM). | ||||
| GC42954 | BMS 470539 (hydrochloride) | 2341796-82-3 | >99.50% | |
BMS 470539 (hydrochloride) is a highly selective and potent melanocortin-1 receptor (MC-1R) agonist. In cAMP accumulation assays, its EC 50 values for human and mouse MC1R are 16.8 and 11.6nM, respectively. | ||||
| GC42975 | BRD32048 | 433694-46-3 | >98.00% | |
BRD32048 عبارة عن غلاف مباشر لـ ETV1 بقوة 17.1 ميكرومتريعدل BRD32048 كلاً من نشاط النسخ بوساطة ETV1 وغزو الخلايا السرطانية التي يقودها ETV1BRD32048 يمنع أستلة ETV1 ويعزز تدهورهايعمل BRD32048 كأفضل مرشح ETV1 المضطرب | ||||
| GC42997 | Butyrolactone I | 87414-49-1 | >98.00% | |
بوتيرولاكتون 1 هو مثبط تنافسي لـ ATP لـ CDK1 كمستقلب ثانوي من A. terreusبوتيرولاكتون 1 له تأثيرات مضادة للأورام في الرئة ذات الخلايا غير الصغيرة والرئة ذات الخلايا الصغيرة وخطوط خلايا سرطان البروستاتا | ||||
| GC43110 | C8 Galactosylceramide (d18:1/8:0) | 41613-16-5 | >98.00% | |
C8 Galactosylceramide is a synthetic C8 short-chain derivative of known membrane microdomain-forming sphingolipids. | ||||
| GC43176 | CAY10575 | 916985-21-2 | >95.00% | |
CAY10575 (المركب 8) هو مثبط IKK2 مع IC50 من 0.075 μ ؛ M. | ||||
| GC43189 | CAY10681 | 1542066-69-2 | >98.00% | |
Inactivation of the tumor suppressor p53 commonly coincides with increased signaling through NF-κB in cancer. | ||||
| GC43190 | CAY10682 | 1542066-74-9 | >98.00% | |
(±)-Nutlin-3 blocks the interaction of p53 with its negative regulator Mdm2 (IC50 = 90 nM), inducing the expression of p53-regulated genes and blocking the growth of tumor xenografts in vivo. | ||||
| GC43212 | CCG-232601 | 1922099-21-5 | >98.00% | |
CCG-232601 (المركب 8f) هو مثبط مسار نسخ Rho / MRTF / SRF فعال وفعال عن طريق الفم | ||||
| GC43368 | D,L-1′-Acetoxychavicol Acetate | 52946-22-2 | >95.00% | |
D,L-1′-Acetoxychavicol acetate is a natural compound first isolated from the rhizomes of ginger-like plants. | ||||
| GC43493 | DL-Sulforaphane N-acetyl-L-cysteine | 334829-66-2 | >98.00% | |
Nrf2 activation of the antioxidant response element (ARE) is central to cytoprotective gene expression against oxidative and/or electrophilic stress. | ||||
| GC43893 | iKIX1 | 656222-54-7 | >99.00% | |
iKIX1 هو عامل مضاد للفطريات ويعيد الحساسية للمكورات العنقودية المقاومة للأدوية | ||||
| GC43894 | IKK2 Inhibitor VI | 354811-10-2 | >95.00% | |
Inhibitor of NF-κB kinase 2 (IKK2, also known as IKKβ) acts as part of an IKK complex in the canonical NF-κB pathway, phosphorylating inhibitors of NF-κB (IκBs) to initiate signaling. | ||||
| GC44216 | ML-180 | 863588-32-3 | >98.00% | |
ML-180 (SR1848) هو ناهض عكسي لمستقبلات الكبد اليتيم 1 (LRH-1 ؛ NR5A2) مع IC50 من 3.7 ميكرومترML-180 غير نشط للعامل الستيرويدي المنشأ -1 (SF-1 ؛ NR5A1 ؛ IC50> 10 ميكرومتر)ML-180 لديه القدرة على الإصابة بسرطانات تعتمد على LRH-1 | ||||
| GC44388 | NF-κB Control | 201608-17-5 | >95.00% | |
NF-κB inhibitor is a synthetic peptide corresponding to the nuclear localization sequence (NLS) of NF-κB p105 subunit (also known as p50) appended to a hydrophobic sequence to facilitate import into living cells. | ||||
