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Results for "

skeleton

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    48
    TargetMol | All_Pathways
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    1
    TargetMol | Compound_Libraries
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    19
    TargetMol | Natural_Products
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    8
    TargetMol | Recombinant_Protein
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    3
    TargetMol | Isotope_Products
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    2
    TargetMol | Standard_Products
2-Ketoglutaric acid Sodium
α-Ketoglutaric acid sodium salt, Oxoglutaric acid, AKG, 2-oxoglutarate monobasic
T492022202-68-2
2-Ketoglutaric acid Sodium (AKG) is a key molecule in the TCA cycle. It can be produced from glutamate by oxidative deamination via glutamate dehydrogenase and as a product of pyridoxal phosphate-dependent transamination reactions (mediated by branched-chain amino acid transaminases) in which glutamate is a common amino donor.
  • $30
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Usnic Acid
Usniacin
T2731125-46-2
Usnic Acid (Usniacin) is an antimicrobial, antitumor and enzyme inhibiting agent shown to uncouple oxidative phosphorylation in mouse-liver mitochondria. Usnic acid induces necrosis in certain cells.
  • $30
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TargetMol | Citations Cited
2-Ketoglutaric acid
T5980328-50-7
2-Ketoglutaric acid is a reversible inhibitor of tyrosinase (IC50=15 mM). 2-Ketoglutaric acid is an intermediate of the Krebs cycle and can produce either ATP or GTP. 2-Ketoglutaric acid also acts as a major carbon backbone for the nitrogen assimilation reaction.
  • $42
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TargetMol | Citations Cited
Batabulin
T138067
T10460195533-53-0
Batabulin (T138067) is an antitumor compound that binds covalently and selectively to a subset of the β-tubulin isotypes, disrupting microtubule polymerization. This disruption affects cell morphology, induces cell-cycle arrest, and ultimately leads to apoptotic cell death.
  • $40
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Bohemine
T2029189232-42-6
Bohemine is a cyclin-dependent kinase inhibitor.
  • $35
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TargetMol | Citations Cited
AG957
T21785140674-76-6
Tyrphostin AG957, a tyrosine kinase inhibitor with anti-BCR/ABL tyrosine kinase activity restores beta1 integrin-mediated adhesion and inhibitory signaling in chronic myelogenous leukemia hematopoietic progenitors[1].
  • $50
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SMIFH2
T23372340316-62-3
SMIFH2 is formin homology 2 (FH2) domains inhibitor.
  • $30
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TargetMol | Citations Cited
Estramustine phosphate sodium
Ro 21-8837/001, Estramustine phosphate disodium
T445152205-73-9
Estramustine phosphate sodium (Ro 21-8837/001) is an antimicrotubule chemotherapy agent; arrests prostate cancer cells in the G2/M phase of the cell cycle.
  • $38
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TargetMol | Citations Cited
MLS000532223
T847316616-39-0
MLS000532223 is a selectiveRho family GTPases inhibitor(EC50 : 16 μM to 120 μM).
  • $113
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Azadirachtin
TN141711141-17-6
Azadirachtin has antifungal activity, used as an insecticide.
  • $58
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2-Methyl-2H-indazole-3-carboxylic acid
Fr2126534252-44-3
2-Methyl-2H-indazole-3-carboxylic acid can be used as a potentially active molecular skeleton for the design and synthesis of biologically active compounds.
  • $30
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TargetMol | Inhibitor Sale
3-Aminophenol
PDK0293591-27-5
3-Aminophenol can provide an aromatic ring skeleton for the synthesis of various dyes and is also a core raw material for the synthesis of para-amino-salicylic acid.
  • $29
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Barbituric acid
T20594067-52-7
Barbituric acid is a pyrimidine derivative and the basic skeleton of barbiturate drugs, commonly used in the preparation of barbiturate drugs and other heterocyclic compounds. It exhibits weak inhibitory activity against tyrosinase in mushrooms.
  • $56
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Adipic dihydrazide
Adipodihydrazide, Adipic acid dihydrazide
T2059701071-93-8
Adipic dihydrazide (ADH) is a dihydrazide with a symmetrical C4 skeleton, commonly used as a bifunctional cross-linking agent for water-in-oil emulsions and a curing agent for epoxy resins. ADH exhibits antibacterial activity against E. coli and P. aeruginosa.
  • $35
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Ursonic Acid
TOS-BB-0966, Prunol, NSC4060, Malol, CCRIS 7123, 3-Ketoursolic acid
T33236246-46-4
Ursonic Acid (TOS-BB-0966) belongs to the family of Ursane Triterpenes whose structure is based on the pentacyclic ursane skeleton. It has potential as HIV-1 Protease Inhibitor.
  • $35
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Chelidamic acid
T5884138-60-3
Chelidamic acid is a heterocyclic organic acid with a pyran skeleton and acts as an inhibitor of glutamate decarboxylase, with a Ki of 33 μM.
  • $29
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Collagen, Type I, from bovine achilles tendon
T87939
Collagen, Type I, from bovine achilles tendon is a type I collagen derived from bovine achilles tendon, which is widely found in marine invertebrate tissues. Collagen, Type I, from bovine achilles tendon is the only component of collagen fibers that make up the dermis, and plays a major role in bone and connective tissue. connective tissues, and functions primarily by forming and maintaining the integrity of the skeleton.
  • $33
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Nortrachelogenin-8'-O-beta-glucoside
TN4674858127-38-5
Nortrachelogenin-8'-O-beta-glucoside is a lignan with a diarylhydroxybutyrolactone skeleton which isolated from the leaves and stems of Trachelospermum jasminoides (Lindl.) Lem.
  • $123
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TargetMol | Inhibitor Sale
TargetMol | Citations Cited
Deprodone propionate
RD-20000, RD20000
T1954620424-00-4
Deprodone propionate (RD20000) is a synthetic corticosteroid suitable for inflammation research.
  • $117
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3-Amino-5-bromo-2-methylpyridine
T200222914358-73-9
3-Amino-5-bromo-2-methylpyridine (3ABMP) is a key reagent for constructing heterocyclic compounds in the field of biochemistry. its unique structure enables it to act as a core skeleton for synthesizing candidate drugs containing pyridine structures such as antibacterial and antiviral drugs.
  • Inquiry Price
7-10 days
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CP-8668
UNII-5371O2R79D, CP 8668
T31082209331-43-1
CP-8668 is an orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzoindolone skeleton.
  • $1,520
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Dihydroisoalantolactone
T314711856-58-2
Dihydroisoalantolactone is found in herbs and spices. Dihydroisoalantolactone is isolated from roots of Inula helenium (elecampane). This compound Aliphatic heteropolycyclic, belongs to the class of organic compounds known as eudesmanolides, secoeudesmano
  • $1,520
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Rubrolone
Ro21-1660/002, Ro-21-1660/002, Ro 21-1660/002
T3444365445-21-8
Rubrolone is a natural tropolonoid with a unique carbon skeleton.
  • Inquiry Price
3-6 months
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WZ4002-hydroxy
WZ-4002-hydroxy, WZ4002 analog, WZ4002 demethyl derivate, WZ 4002-hydroxy
T35147
WZ4002-hydroxyl is a WZ4002 derivative or WZ4002 analogue in which methoxy is replaced by hydroxyl and can be detected in 50% of patients with clinical resistance to gefitinib or erlotinib. WZ4002 has a basic chemical skeleton (covalent pyrimidine) that d
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