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s-99

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    12
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    1
    TargetMol | Peptide_Products
S-99
T224181124381-69-6
S-99 is a high purity chemical that targets ASK and is important for Immunology, Inflammation, Cancer research.
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TargetMol | Inhibitor Sale
GS-9901
T154201640247-87-5In house
GS-9901 is a selective, orally active and potent PI3Kδ inhibitor (IC50: 1 nM) for the study of non-Hodgkin's lymphoma and chronic lymphocytic leukemia.
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6-8 weeks
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AS-99 free base
T369772323623-93-2
AS-99 is a first-in-class, potent, and selective ASH1L histone methyltransferase inhibitor (IC50= 0.79 μM, Kd= 0.89 μM) with anti-leukemic activity, blocking cell proliferation, inducing apoptosis and differentiation, downregulating MLL fusion target genes, and reducing the leukemia burden in vivo[1].
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AS-99 TFA
T36978
AS-99 TFA is a first-in-class, potent, and selective ASH1L histone methyltransferase inhibitor (IC50= 0.79 μM, Kd= 0.89 μM) with anti-leukemic activity. It blocks cell proliferation, induces apoptosis and differentiation, downregulates MLL fusion target genes, and reduces the leukemia burden in vivo[1].
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TES-991
T131321883602-20-7
TES-991 is a potent and selective inhibitor of human α-Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD), with an IC50 of 3 nM.
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6-8 weeks
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mips-9922
T280441416956-33-6
MIPS-9922 is a potent and selective PI3Kβ inhibitor with antiplatelet activity. MIPS-9922 inhibited integrin αIIbβ3 activation and αIIbβ3 dependent platelet adhesion to immobilized vWF under high shear. MIPS-9922 also potently inhibited ADP-induced washe
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6-8 weeks
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AS-99
T73529
AS-99 is a first-in-class, potent, and selective inhibitor of the ASH1L histone methyltransferase, displaying anti-leukemic activity with an IC50 of 0.79 µM and a Kd of 0.89 µM. It inhibits cell proliferation, induces apoptosis and differentiation, downregulates MLL fusion target genes, and effectively reduces leukemia burden [in vivo].
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8-10 weeks
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Oclacitinib
PF-03394197
T20121208319-26-9
Oclacitinib (PF-03394197)(PF03394197) is a potent and selective JAKs inhibitor with IC50 of 10-99 nM; not inhibit a panel of 38 non-JAK kinases (IC50 's > 1000 nM).
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Rugulotrosin A
T37254685135-81-3
Rugulotrosin A is an antibiotic originally isolated from Penicillium, active against the Gram-positive bacteria E. faecalis, B. cereus, B. subtilis, and S. aureus with 99% lethal dose (LD99) values of 1.6, 3.1, 5.5, and 200 μg ml, respectively. Rugulotrosin A is inactive against Gram-negative bacteria.
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(S)-2-Amino-2-cyclopropylacetic acid
T6652749606-99-7
(S)-2-Amino-2-cyclopropylacetic acid is a useful organic compound for research related to life sciences. The catalog number is T66527 and the CAS number is 49606-99-7.
    7-10 days
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    Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)
    T67239909389-99-7
    Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II) is a useful organic compound for research related to life sciences. The catalog number is T67239 and the CAS number is 909389-99-7.
      7-10 days
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      FLA-99
      T70584146931-12-6
      FLA-99 inhibits breakdown of inositol-1,4,5-triphosphate by inositol-1,4,5-triphosphate 5-phosphatase.
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      6-8 weeks
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