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Results for "

Melanoma Metastasis

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Antibiotic (1) Bacterial (2) Endogenous Metabolite (1) Fungal (2) HIF/HIF Prolyl-Hydroxylase (1) ICMT (56) LPL Receptor (1) Microtubule/Tubulin (1) MMP (1) NF-κB (1) Parasite (2) Phosphodiesterase (PDE) (1) PPAR (2) Ras (1) RIP kinase (1) ROCK (2) Toll-like Receptor (TLR) (1)
By Research Areas:	Cancer (70) Infection (2) Neurological Disease (1)

Inhibitors & Agonists

Peptides

Natural
Products

Targets Recommended: AIM2

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-121524

DJ101	Microtubule/Tubulin	Cancer
DJ101 is a potent and metabolically stable tubulin inhibitor. DJ101 targets the colchicine binding site and overcomes taxane resistance. DJ101 also inhibits melanoma tumor growth and lung metastasis. DJ101 can be used for prostate cancer research .

HY-121750

CCG-222740	Ras ROCK	Cancer
CCG-222740 is an orally active and selective Rho/myocardin-related transcription factor (MRTF) pathway inhibitor . CCG-222740 is also a potent inhibitor of alpha-smooth muscle actin protein expression. CCG-222740 effectively reduces fibrosis in skin and blocks melanoma metastasis .

HY-B0963

Cloxiquine 5-Chloro-8-quinolinol	Bacterial Fungal Parasite PPAR	Infection Cancer
Cloxiquine (5-Chloro-8-quinolinol) is an antibacterial, antifungal and antiamoebic agent. Cloxiquine can be used for the research of tuberculosis and dermatoses. Cloxiquine suppresses the growth and metastasis of melanoma cells through activation of PPARγ .

HY-156483

TT-012	Others	Cancer
TT-012 specifically binds to dynamic MITF and destroys the latter's dimer formation and DNA-binding ability. TT-012 inhibits the transcriptional activity of MITF in B16F10 melanoma cells. TT-012 inhibits the growth of high-MITF melanoma cells, and inhibits the tumor growth and metastasis with tolerable toxicity to liver and immune cells in animal models .

HY-119933

RIPK1-IN-7	RIP kinase	Cancer
RIPK1-IN-7 is a potent and selective RIPK1 inhibitor with a K_d of 4 nM and an enzymatic IC₅₀ of 11 nM. RIPK1-IN-7 exhibits excellent antimetastasis activity in the experimental B16 melanoma lung metastasis model .

HY-112052

Aminomalonic acid	Endogenous Metabolite	Cancer
Aminomalonic acid is an amino endogenous metabolite, acts as a strong inhibitor of L-asparagine synthetase from Leukemia 5178Y/AR (K_i= 0.0023 M) and mouse pancreas (K_i= 0.0015 M) in vitro. Aminomalonic acid is a potential biomarker to discriminate between different stages of melanoma metastasis .

HY-156247

IVMT-Rx-3	NF-κB MMP	Cancer
IVMT-Rx-3 is a inhibitor of SDCBP targeting of the PDZ1 and PDZ2 Domains of MDA-9/Syntenin. IVMT-Rx-3 blocks MDA-9/Syntenin interaction with Src, reduces NF-κB activation, and inhibits MMP-2/MMP-9 expression. IVMT-Rx-3 inhibits Melanoma Metastasis ^[1]

HY-124875

Arylsulfonamide 64B HIF inhibitor 64B	HIF/HIF Prolyl-Hydroxylase	Neurological Disease
Arylsulfonamide 64B (HIF inhibitor 64B) is an inhibitor of the hypoxia-induced factor (HIF)*. Arylsulfonamide 64B inhibits hypoxia/HIF-induced expression of c-Met and CXCR4 and reduces primary tumor growth and metastasis* of uveal melanoma mouse model .**

HY-120241

Reticulol K 251-1	Phosphodiesterase (PDE)	Cancer
Reticulol (K 251-1) is an inhibitor of cyclic adenosine 3', 5'-monophosphate phosphodiesterase. Reticulol shows antitumor activity independent with cell cycle arrest or apoptosis. Reticulol inhibits cell growth of murine melanoma cells and human lung tumor cells. Reticulol protects its lung metastasis via the bloodstream by inhibiting the growth of B16F10 melanoma .

HY-119261

Ruboxyl	Antibiotic	Cancer
Ruboxyl is an anthracycline antibiotic with antitumor activity. Ruboxyl inhibits colorectal cancer (CRC) liver metastasis in mice by 84%, suppresses B16 melanoma growth, and increases the survival rate of mice with L1210 or L5178Y leukemia .

HY-B0963R

Cloxiquine (Standard)	Bacterial Fungal Parasite PPAR	Infection Cancer
Cloxiquine (Standard) is the analytical standard of Cloxiquine. This product is intended for research and analytical applications. Cloxiquine (5-Chloro-8-quinolinol) is an antibacterial, antifungal and antiamoebic agent. Cloxiquine can be used for the research of tuberculosis and dermatoses. Cloxiquine suppresses the growth and metastasis of melanoma cells through activation of PPARγ .

HY-139061

Palmitoyl 3-carbacyclic phosphatidic acid	LPL Receptor ROCK	Cancer
Palmitoyl 3-carbacyclic phosphatidic acid (HY-139061) is a palmitoylated Carba-like cyclophosphatidic acid and an analog of lysophosphatidic acid (LPA). Palmitoyl 3-carbacyclic phosphatidic acid has different functions from LPA and can inhibit the activation of RhoA and inhibit the migration of melanoma cells. Palmitoyl 3-carbacyclic phosphatidic acid effectively inhibited experimental lung metastasis and reduced the number of tumor nodules in a B16-F0 xenograft mouse model .

HY-150158

TMX-201	Toll-like Receptor (TLR)	Cancer
TMX-201 is a TLR7 ligand-phospholipid conjugate. TMX-201 shows potent immune stimulatory activity. TMX-201 can be used for breast cancer and melanoma research .

HY-117231

RM 06	Others	Cancer
RM 06 is an immunomodulator with a peptidyl hypoxanthine structure that significantly reduces the number of lung metastases of B16 melanoma cells in mice after lethal irradiation and bone marrow reconstitution by stimulating the activity of natural killer (NK) cells .

HY-157092B

(R)-ICMT-IN-3	ICMT	Cancer
(R)-ICMT-IN-3 (compound ent 2-27) is an inhibitor of ICMT (IC₅₀=0.01 μM) .

HY-157092A

(S)-ICMT-IN-3	ICMT	Cancer
(S)-ICMT-IN-3 (compound ent 1-27) is an inhibitor of ICMT (IC₅₀=0.23 μM) .

HY-156500

ICMT-IN-1	ICMT	Cancer
ICMT-IN-1 (compound 75) is an inhibitor of ICMT (IC₅₀=0.0013 μM). ICMT-IN-1 dose-dependently induces ICMT accumulation in the cytoplasm of HCT-116 cells and inhibits the proliferation of multiple cancer cell lines expressing K-Ras and N-Ras .

HY-157097

ICMT-IN-10	ICMT	Cancer
ICMT-IN-10 (compound 32) is an inhibitor of ICMT (IC₅₀=0.184 μM) .

HY-155421

ICMT-IN-11	ICMT	Cancer
ICMT-IN-11 (compound 48) is an inhibitor of ICMT (IC₅₀=0.031 μM) .

HY-149706

ICMT-IN-12	ICMT	Cancer
ICMT-IN-12 (compound 78) is an inhibitor of ICMT (IC₅₀=0.42 μM) .

HY-155422

ICMT-IN-13	ICMT	Cancer
ICMT-IN-13 (compound 49) is an inhibitor of ICMT (IC₅₀=0.47 μM) .

HY-155423

ICMT-IN-14	ICMT	Cancer
ICMT-IN-14 (compound 50) is an inhibitor of ICMT (IC₅₀=0.025 μM) .

HY-155424

ICMT-IN-15	ICMT	Cancer
ICMT-IN-15 (compound 51) is an inhibitor of ICMT (IC₅₀=0.032 μM) .

HY-157098

ICMT-IN-16	ICMT	Cancer
ICMT-IN-16 (compound 33) is an inhibitor of ICMT (IC₅₀=0.131 μM) .

HY-155425

ICMT-IN-17	ICMT	Cancer
ICMT-IN-17 (compound 52) is an inhibitor of ICMT (IC₅₀=0.38 μM) .

HY-157099

ICMT-IN-18	ICMT	Cancer
ICMT-IN-18 (compound 35) is an inhibitor of ICMT (IC₅₀=0.066 μM) .

HY-155426

ICMT-IN-19	ICMT	Cancer
ICMT-IN-19 (compound 53) is an inhibitor of ICMT (IC₅₀=0.026 μM) .

HY-155418

ICMT-IN-2	ICMT	Cancer
ICMT-IN-2 (compound 45) is an inhibitor of ICMT (IC₅₀=0.168 μM) .

HY-155427

ICMT-IN-20	ICMT	Cancer
ICMT-IN-20 (compound 54) is an inhibitor of ICMT (IC₅₀=0.682 μM) .

HY-149707

ICMT-IN-21	ICMT	Cancer
ICMT-IN-21 (compound 6ag) is an ICMT inhibitor (IC₅₀=8.8 μM), a sulfonamide-modified farnesyl cysteine (SMFC). The farnesyl and carboxylic acid motifs of ICMT-IN-21 are important structures for inhibiting ICMT .

HY-155428

ICMT-IN-22	ICMT	Cancer
ICMT-IN-22 (compound 62) is an inhibitor of ICMT (IC₅₀=0.63 μM) .

HY-157100

ICMT-IN-23	ICMT	Cancer
ICMT-IN-23 (compound 36) is an inhibitor of ICMT (IC₅₀=0.123 μM) .

HY-155429

ICMT-IN-24	ICMT	Cancer
ICMT-IN-24 (compound 63) is an inhibitor of ICMT (IC₅₀=0.19 μM) .

HY-157101

ICMT-IN-25	ICMT	Cancer
ICMT-IN-25 (compound 37) is an inhibitor of ICMT (IC₅₀=0.025 μM) .

HY-157102

ICMT-IN-26	ICMT	Cancer
ICMT-IN-26 (compound 38) is an inhibitor of ICMT (IC₅₀=0.36 μM) .

HY-155430

ICMT-IN-27	ICMT	Cancer
ICMT-IN-27 (compound 64) is an inhibitor of ICMT (IC₅₀=0.1 μM) .

HY-155431

ICMT-IN-28	ICMT	Cancer
ICMT-IN-28 (compound 65) is an inhibitor of ICMT (IC₅₀=0.008 μM) .

HY-155432

ICMT-IN-29	ICMT	Cancer
ICMT-IN-29 (compound 66) is an inhibitor of ICMT (IC₅₀=0.019 μM) .

HY-157092

ICMT-IN-3	ICMT	Cancer
ICMT-IN-3 (compound 27) is an inhibitor of ICMT (IC₅₀=0.015 μM) .

HY-155433

ICMT-IN-30	ICMT	Cancer
ICMT-IN-30 (compound 67) is an inhibitor of ICMT (IC₅₀=0.27 μM) .

HY-155434

ICMT-IN-31	ICMT	Cancer
ICMT-IN-31 (compound 68) is an inhibitor of ICMT (IC₅₀=0.0038 μM) .

HY-155435

ICMT-IN-32	ICMT	Cancer
ICMT-IN-32 (compound 70) is an inhibitor of ICMT (IC₅₀=0.777 μM) .

HY-155436

ICMT-IN-33	ICMT	Cancer
ICMT-IN-33 (compound 73) is an inhibitor of ICMT (IC₅₀=0.46 μM) .

HY-157103

ICMT-IN-34	ICMT	Cancer
ICMT-IN-34 (compound 39) is an inhibitor of ICMT (IC₅₀=0.17 μM) .

HY-149709

ICMT-IN-35	ICMT	Cancer
ICMT-IN-35 (compound 10n) is a FTPA-triazole compound and ICMT inhibitor (IC₅₀=0.8 μM). ICMT-IN-35 is taken up by mammalian cells and can prevent K-Ras membrane localization and induce K-Ras mislocalization. Furthermore, ICMT-IN-35 is selectively cytotoxic against ICMT ^+/+ MEF cells and has low micromolar activity (IC₅₀=0.8 μM) against metastatic pancreatic cancer cell lines .

HY-157104

ICMT-IN-36	ICMT	Cancer
ICMT-IN-36 (compound 40) is an inhibitor of ICMT (IC₅₀=0.181 μM) .

HY-157105

ICMT-IN-37	ICMT	Cancer
ICMT-IN-37 (compound 41) is an inhibitor of ICMT (IC₅₀=0.308 μM) .

HY-157106

ICMT-IN-38	ICMT	Cancer
ICMT-IN-38 (compound 42) is an inhibitor of ICMT (IC₅₀=0.049 μM) .

HY-157107

ICMT-IN-39	ICMT	Cancer
ICMT-IN-39 (compound 18) is an inhibitor of ICMT (IC₅₀=0.031 μM) .

HY-157094

ICMT-IN-4	ICMT	Cancer
ICMT-IN-4 (compound 28) is an inhibitor of ICMT (IC₅₀=0.27 μM) .

Cat. No.	Product Name	Target	Research Area

HY-P10542

Dodecapeptide AR71	Peptides	Cancer
Dodecapeptide AR71 is an inhibitor of melanoma inhibitory activity (MIA). Dodecapeptide AR71 can reduce cell migration, reduce metastasis formation, and increase immune response. Dodecapeptide AR71 can be used in research on the treatment of malignant melanoma .

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Melanoma Metastasis

Inhibitors & Agonists

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