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Navoximod

CAT: 0013-GTR19156170-03Size: 1 gDry Ice: NoHazardous: No
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CAT#:0013-GTR19156170-03Size:1 g
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Description
Navoximod (NLG- 919, GDC-0919) is a potent indoleamine- (2,3) -dioxygenase (IDO) pathway inhibitor (Ki/EC50: 7 nM/75 nM) . (In Vitro) :Using IDO-expressing human monocyte-derived dendritic cells (DCs) in allogeneic mixed lymphocyte reaction (MLR) reactions, Navoximod (NLG919) potently blocks IDO-induced T cell suppression and restores robust T cell responses with an ED50=80 nM. Similarly, using IDO-expressing mouse DCs from tumor-draining lymph nodes, Navoximod abrogates IDO-induced suppression of antigen-specific T cells (OT-I) in vitro, with ED50=120 nM. Navoximod inhibits the IDO activity in a concentration-dependent manner with an EC50 of 0.95 μM. PEG2k-Fmoc-NLG (L) is less active (EC50 of 3.4 μM) in inhibiting IDO compared with free Navoximod while PEG2k-Fmoc-NLG (S) is least active (EC50>10 μM) . Coculture of IDO+tumor cells with splenocytes isolated from BALB/c mice leads to significant inhibition of T-cell proliferation. This inhibition is significantly attenuated when the mixed cells are treated with Navoximod. PEG2k-Fmoc-NLG (L) is also active in reversing the inhibitory effect of tumour cells although slightly less potent than Navoximod . (In Vivo) :VNavoximod (NLG919) is orally bioavailable (F>70%) ; and has a favorable pharmacokinetic and toxicity profile. In mice, a single oral administration of Navoximod reduces the concentration of plasma and tissue Kyn by ~50%. In vivo, in mice bearing large established B16F10 tumors, administration of Navoximod markedly enhances the anti-tumor responses of na ve, resting pmel-1 cells to vaccination with cognate hgp100 peptide plus CpG-1826 in IFA. In this stringent established-tumor model, Navoximod plus pmel-1/vaccine produce a dramatic collapse of tumor size within 4 days of vaccination (~95% reduction in tumor volume compare to control animals receiving pmel-1/vaccine alone without Navoximod) . When combined with NSC 362856 (TMZ) +radiation therapy (RT), both Navoximod and D-1MT (Indoximod) enhance survival relative to mice treated with TMZ+RT alone.
CAS Number
1402837-78-8
Product Name Alternative
GDC-0919 | NLG-?919
Purity
>98% (HPLC)
Solubility
DMSO:100 mg/mL (316.09 mM; Need ultrasonic)
Smiles
O[C@@H] ([C@H]1CC[C@H] (O) CC1) C[C@@H] (C2=C3C=CC=C2F) N4C3=CN=C4
Molecular Formula
C18H21FN2O2
Molecular Weight
316.37
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.

Chemical Information

trans-4-((1R)-2-((5S)-6-Fluoro-5H-imidazo(5,1-a)isoindol-5-yl)-1-hydroxyethyl)cyclohexanol

Navoximod is under investigation in clinical trial NCT02048709 (Indoleamine 2,3-Dioxygenase (IDO) Inhibitor in Advanced Solid Tumors).

CAS Number1402837-78-8
PubChem CID70914230
IUPAC Name4-[(1R)-2-[(5S)-6-fluoro-5H-imidazo[5,1-a]isoindol-5-yl]-1-hydroxyethyl]cyclohexan-1-ol
Molecular FormulaC18H21FN2O2
Molecular Weight316.4
XLogP2.1
Topological Polar Surface Area58.3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Heavy Atom Count23
Formal Charge0
Complexity416
SMILES
C1CC(CCC1[C@@H](C[C@H]2C3=C(C=CC=C3F)C4=CN=CN24)O)O
InChI
InChI=1S/C18H21FN2O2/c19-14-3-1-2-13-16-9-20-10-21(16)15(18(13)14)8-17(23)11-4-6-12(22)7-5-11/h1-3,9-12,15,17,22-23H,4-8H2/t11?,12?,15-,17+/m0/s1
InChIKey
YGACXVRLDHEXKY-LHPNLFKDSA-N
Chemical Structure
2D Structure
2D structure of trans-4-((1R)-2-((5S)-6-Fluoro-5H-imidazo(5,1-a)isoindol-5-yl)-1-hydroxyethyl)cyclohexanol
CAS: 1402837-78-8
CID: 70914230
Formula: C18H21FN2O2
MW: 316.4
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight316.4
XLogP32.1
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass316.15870608
Monoisotopic Mass316.15870608
Topological Polar Surface Area58.3 Ų
Heavy Atom Count23
Formal Charge0
Complexity416
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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