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Results for "

map3k14 in-173

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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MAP3K14-IN-173
T698942113617-02-8
MAP3K14-IN-173 is a potent MAP3K14 kinase inhibitor.
  • Inquiry Price
10-14 weeks
Size
QTY
ACTH 1-14 acetate(25696-21-3 free base)
Adrenocorticotropic Hormone Fragment 1-14 acetate
TP1238L
ACTH 1-14 acetate(25696-21-3 free base) (Adrenocorticotropic Hormone Fragment 1-14 acetate) is a fragment of adrenocorticotrophin, which regulates cortisol and androgen production.Adrenocorticotropic hormone (ACTH), also known as corticotropin, is produced and secreted by the anterior pituitary gland. ACTH is an important component of the hypothalamic-pituitary-adrenal axis as a response to biological stress.
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TargetMol | Inhibitor Sale
VA-K-14 hydrochloride
VAK14 Hydrochloride,VA K 14 HCl,VA-K-14 HCl,VAK14 HCl
T290871171341-19-7In house
VA-K-14 hydrochloride(VAK14 HCl) is a selective thyrotropin receptor (TSHR) antagonist (IC50= 12.3 μM) that inhibits TSHR stimulation by serum and monoclonal TSHR-stimulating antibodies from patients with GD and abrogates TSHR signaling.
  • Inquiry Price
6-8weeks
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1,2-Dinor-3-oxo-6,10-farnesadien-14-oic acid; Z-Fo
T1262031217271-08-3
1,2-Dinor-3-oxo-6,10-farnesadien-14-oic acid; Z-Fo is a useful organic compound for research related to life sciences. The catalog number is T126203 and the CAS number is 1217271-08-3.
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Ergosta-4,6,8(14),22-tetraen-3-one
TN161719254-69-4
Ergosta-4,6,8(14),22-tetraen-3-one exhibits cytotoxic activity against human gastric cancer cells and can induce G2 M cell cycle arrest and apoptosis in human hepatocellular carcinoma (HepG2) cells. These findings could facilitate the further use of various medicinal fungi in cancer treatment.
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K-Ras G12C-IN-3
T117371629268-19-4
Heterocyclic compounds as covalent inhibitors of G12C mutant K-Ras protein useful for treating cancers.K-Ras G12C-IN-3 is a novel and irreversible inhibitor of mutant K-ras G12C.
  • Inquiry Price
6-8 weeks
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8(14),15-Isopimaradien-3-ol
TN32604728-30-7
ent-8(14),15-pimaradien-3beta-ol (8(14),15-Isopimaradien-3-ol) can induce vascular relaxation. It displays high antibacterial activities (MIC values lower than 10 microg /mL for most pathogens).
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K 259-3
K2593
T32348127172-90-1
K 259-3, a methyl ester of K 259-2, is an inhibitor of calmodulin-dependent cyclic nucleotide phosphodiesterase.
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1,2-Dinor-3-oxo-6,10-farnesadien-14-oic acid; E-Fo
T1262041217271-07-2
1,2-Dinor-3-oxo-6,10-farnesadien-14-oic acid; E-Fo is a useful organic compound for research related to life sciences. The catalog number is T126204 and the CAS number is 1217271-07-2.
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K-Ras-IN-3
T892463024991-82-7
K-Ras-IN-3 (compound 3) is an effective inhibitor of GDP-KRAS G12V, exhibiting an IC50 value of 0.371 nM. It has potential for use in cancer research.
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10-14 weeks
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14-3-3σ/ERα stabilizer-1
T79736
Compound 181, also known as 14-3-3σ/ERα Stabilizer-1, is a covalent stabilizer targeting the 14-3-3σ/ERα proteins. It is utilized in research as a molecular glue [1].
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3-Hydroxypregn-14-ene-20-one
T131408
3-Hydroxypregn-14-ene-20-one is a useful organic compound for research related to life sciences and the catalog number is T131408.
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K-Ras ligand-Linker Conjugate 3
T180562378261-87-9
K-Ras ligand-Linker Conjugate 3 (Compound 001371) is a chemical compound comprising a ligand for the K-Ras recruiting moiety and a PROTAC linker, responsible for recruiting E3 ligases (e.g., VHL, CRBN, MDM2, and IAP). This compound is essential for synthesizing PROTAC K-Ras Degrader-1, a potent degrader with a degradation efficacy of ≥70% in SW1573 cells[1].
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Cathepsin K inhibitor 3
T722961694638-70-4
Cathepsin K Inhibitor 3, exhibiting an IC50 value of 0.5 nM, is a highly selective inhibitor of cathepsin K, featuring a favorable pharmacokinetic profile. It holds potential for use in studies of osteoarthritis (OA).
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8-10 weeks
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ACTH (1-14) TFA (25696-21-3 free base)
Adrenocorticotropic Hormone Fragment 1-14 (TFA),ACTH (1-14) TFA
TP1237
ACTH (1-14) (TFA) is a polypeptide of corticotrophin, which promotes the release of cortisol.
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NSC109131
T6989321170-27-4
NSC109131 is an inhibitor of human tyrosyl-DNA phosphodiesterase 1 (TDP1).
  • Inquiry Price
6-8 weeks
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