94 Results for "

hedgehog pathway

" in MedChemExpress (MCE) Product Catalog:
Products (94)

94 Results for "hedgehog pathway" in MCE Product Catalog:

67
67 Publications Verification
Referencia número: HY-13901
No. CAS: 500579-04-4
Pureza:  99.66%
Synonyms: NSC 136476
Target:  

Gli Autophagy

Áreas de investigación:  

Cancer

GANT 61 is an inhibitor of Gli1 and Gli2 targeting the Hedgehog/GLI pathway.
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56
56 Cited Publications
Referencia número: HY-17024
No. CAS: 4449-51-8
Synonyms: 11-Deoxojervine
Cyclopamine is a Hedgehog (Hh) pathway antagonist with an IC50 of 46 nM in the Hh cell assay. Cyclopamine is also a selective Smo inhibitor.
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53
53 Cited Publications
Referencia número: HY-10440
No. CAS: 879085-55-9
Pureza:  99.83%
Synonyms: GDC-0449
Target:  

Hedgehog Autophagy

Áreas de investigación:  

Neurological Disease Inflammation/Immunology Cancer

Vismodegib (GDC-0449) is a BBB-permeable and orally active hedgehog pathway inhibitor with an IC50 of 3 nM. Vismodegib also inhibits P-gp, ABCG2 with IC50 values of 3.0 μM and 1.4 μM, respectively .
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44
44 Cited Publications
Referencia número: HY-12848
No. CAS: 912545-86-9
Pureza:  99.60%
Target:  

Smo

Áreas de investigación:  

Cancer

SAG is a potent Smoothened (Smo) receptor agonist (EC50=3 nM; Kd=59 nM). SAG activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo .
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44
44 Cited Publications
Referencia número: HY-12848B
No. CAS: 2095432-58-7
Pureza:  99.91%
Target:  

Smo

Áreas de investigación:  

Cancer

SAG hydrochloride is a potent Smoothened (Smo) receptor agonist (EC50=3 nM; Kd=59 nM). SAG hydrochloride activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo .
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44
44 Cited Publications
Referencia número: HY-12848C
No. CAS: 2702366-44-5
Pureza:  99.31%
Target:  

Smo

Áreas de investigación:  

Cancer

SAG dihydrochloride is a potent Smoothened (Smo) receptor agonist (EC50=3 nM; Kd=59 nM). SAG dihydrochloride activates the Hedgehog signaling pathway and counteracts Cyclopamine (HY-17024) inhibition of Smo .
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24
24 Cited Publications
Referencia número: HY-17514
No. CAS: 84625-61-6
Synonyms: R51211
Itraconazole (R51211) is a triazole antifungal agent and a potent and orally active Hedgehog (Hh) signaling pathway antagonist with an IC50 of ~800 nM. Itraconazole potently inhibits lanosterol 14α-demethylase (cytochrome P450 enzyme), thereby inhibits the oxidative conversion of lanosterol to ergosterol. Itraconazole has anticancer and antiangiogenic effects. Itraconazole is a oxysterol-binding protein (OSBP) inhibitor .
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7
7 Cited Publications
Referencia número: HY-17595
No. CAS: 31431-39-7
Áreas de investigación:  

Infection Cancer

Mebendazole is a highly effective, broad-spectrum antihelmintic against nematode infestations. Mebendazole also exhibits inhibitory effect against glioblastoma multiforme (GBM), inhibits Hedgehog pathway and tubulin polymerization. Mebendazole is orally active and can cross CNS penetration .
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5
5 Cited Publications
Referencia número: HY-12316
No. CAS: 516-72-3
Pureza:  99.29%
Synonyms: 20α-Hydroxycholesterol
20(S)-Hydroxycholesterol (20α-Hydroxycholesterol) is an allosteric activator that selectively targets the Smoothened (Smo) of the Hedgehog pathway with an EC50 of ~30 μM (Hedgehog). 20(S)-Hydroxycholesterol binds to the extracellular cysteine-rich domain (CRD) of Smo in a stereoselective manner, activating downstream Gli transcription factors (without inducing transcription of receptor genes in the Wnt pathway). 20(S)-Hydroxycholesterol enhances osteogenic differentiation of bone marrow stromal cells and synergistically activates the Raf/MEK/ERK pathway with Simvastatin (HY-17502) to promote bone regeneration. 20(S)-Hydroxycholesterol can be used to study the mechanisms of developmental biology, oncology, bone, and angiogenesis .
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4
4 Cited Publications
Referencia número: HY-113081
No. CAS: 15763-06-1
Pureza:  99.21%
1-Methyladenosine is an RNA modification that can serve as a tumor marker, with elevated levels in the body associated with cancer development. Following 1-methyladenosine methylation, upregulation of PPARδ expression regulates cholesterol metabolism and activates Hedgehog signaling pathway, driving liver tumorigenesis .
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3
3 Cited Publications
Referencia número: HY-N0836
No. CAS: 469-59-0
Synonyms: 11-Ketocyclopamine
Jervine (11-Ketocyclopamine) is an orally active steroidal alkaloid and Hedgehog signaling pathway inhibitor. Jervine can be isolated from Veratrum californicum. Jervine regulates Wnt, inhibits the AKT/mTOR signaling pathway, and activates the AMPK signaling pathway. Jervine induces DNA damage, Apoptosis, Autophagy, ROS production and Mitochondrial damage. Jervine exhibits anti-cancer and anti-inflammatory activities. Jervine reduces tumor growth rate and weight in xenograft models. Jervine can be used in studies related to triple-negative breast cancer, nasopharyngeal carcinoma and non-small cell lung cancer .
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3
3 Cited Publications
Referencia número: HY-100790
No. CAS: 302803-72-1
Pureza:  98.57%
Synonyms: HPI-4
Target:  

Hedgehog

Áreas de investigación:  

Cancer

Ciliobrevin A (HPI-4) is a hedgehog (Hh) signaling pathway inhibitor with median inhibitory concentration (IC50) less than 10 μM .
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2
2 Cited Publications
Referencia número: HY-13242
No. CAS: 1258861-20-9
Pureza:  99.92%
Synonyms: LY2940680
Target:  

Smo Gli

Áreas de investigación:  

Cancer

Taladegib is a Smoothened (SMO) antagonist. Taladegib hydrochloride inhibits the Hedgehog signaling pathway, with an IC50 of 5.5 nM for suppressing GLI1 mRNA expression in DAOY cells and an IC50 of 7.6 nM in CGNP cell proliferation assays. Taladegib binds to the extracellular loop region (site 1) of the transmembrane domain of the SMO receptor, competes with cyclopamine for SMO binding, and thereby inhibits Gli-dependent transcription. Taladegib can be used in studies of Hedgehog pathway-related cancers .
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2
2 Cited Publications
Referencia número: HY-N0247
No. CAS: 58558-08-0
Saikosaponin B1 is a bioactive constituent of Radix Bupleuri. Saikosaponin B1 is an agonist of the 5-HT2C receptor with an EC50 of 147.41 μM. Saikosaponin B1 inhibits the Hedgehog (Hh) signaling pathway by targeting the transmembrane protein SMO. Sailosaponin B1 can reduce liver fibrosis. Saikosaponin B1 has anti-cancer activities thus can be studies in research for cancers such as Medulloblastoma (MB) .
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2
2 Cited Publications
Referencia número: HY-13307
No. CAS: 315703-52-7
Pureza:  99.93%
Target:  

Hedgehog

Áreas de investigación:  

Cancer

JK184 is a potent Hedgehog (Hh) pathway inhibitor with IC50 of 30 nM in mammalian cells.
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2
2 Cited Publications
Referencia número: HY-B0508
No. CAS: 16773-42-5
Synonyms: Ro 7-0207
Ornidazole (Ro 7-0207) is a nitroimidazole derivative with anti-trichomonad activity and in vitro activity against a variety of anaerobic bacteria. Ornidazole inhibits Sonic hedgehog (Shh) signaling pathway, exhibits antitumor activity. Ornidazole can be used in research of Crohn’s disease .
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2
2 Cited Publications
Referencia número: HY-18366A
No. CAS: 1782573-67-4
Target:  

Hedgehog

Áreas de investigación:  

Cancer

RU-SKI 43 hydrochloride is a potent and selective Hedgehog acyltransferase (Hhat) inhibitor with an IC50 of 850 nM. RU-SKI 43 hydrochloride reduces Gli-1 activation through Smoothened-independent non-canonical signaling and decreases Akt and mTOR pathway activity. RU-SKI 43 hydrochloride has anti-cancer activity .
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2
2 Cited Publications
Referencia número: HY-N6954
No. CAS: 76996-27-5
Garcinone C, a xanthone derivative, is a natural compound extracted from Garcinia oblongifolia that is used as an anti-inflammatory, astringency and granulation-promoting medicine, and has potential cytotoxic effects on certain cancers. Garcinone C stimulates the expression levels of ATR and 4E-BP1, arrests the cell cycle, inhibits cell viability of the human Nasopharyngeal carcinoma (NPC) cell lines CNE1, CNE2, HK1 and HONE1 in a time‑ and dose‑dependent manner through inhibition of Hedgehog signaling pathway. Garcinone C is orally active .
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1
1 Cited Publications
Referencia número: HY-B0877
No. CAS: 3093-35-4
Synonyms: SQ-18566
Halcinonide (SQ-18566) is an orally active Smoothened (Smo) agonist. Halcinonide activates the Hedgehog signaling pathway by binding to Smo and promoting its internalization and expression, thereby activating Gli transcription factors. Halcinonide not only stimulates cell proliferation, increases the expression of cyclin D2/CDK6 and inhibits the degradation of caspase-3, but also suppresses Bcl-2/Bax-mediated apoptosis, oxidative stress and inflammatory responses. Halcinonide activates RxRγ to upregulate the expression of myelin genes, thereby reducing cerebral infarction and improving behavioral deficits. Halcinonide has been used in studies related to multiple sclerosis and ischemic stroke .
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1
1 Cited Publications
Referencia número: HY-113965
No. CAS: 334998-36-6
Pureza:  99.04%
Target:  

Hedgehog Smo Apoptosis

Áreas de investigación:  

Inflammation/Immunology

CUR61414 is a novel, potent and cell permeable Hedgehog signaling pathway inhibitor (IC50 =100-200 nM). CUR61414 is a small-molecule aminoproline class compound and selectively binds to smoothened (Smo) with a Ki value of 44 nM. CUR-61414 can induce apoptosis in cancer cells without affecting neighboring non-tumor cells .
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