Benzomalvin E, an indoleamine 2,3-dioxygenase inhibitor isolated from Penicillium sp. FN070315 (Q83408882)

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22 January 2020

title

Benzomalvin E, an indoleamine 2,3-dioxygenase inhibitor isolated from Penicillium sp. FN070315 (English)

1 reference

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22 January 2020

author name string

Jun-Pil Jang

1

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22 January 2020

Jae-Hyuk Jang

2

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22 January 2020

Nak-Kyun Soung

3

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22 January 2020

Hye-Min Kim

4

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22 January 2020

Sook-Jung Jeong

5

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22 January 2020

Yukihiro Asami

6

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22 January 2020

Kee-Sun Shin

7

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22 January 2020

Mee Ree Kim

8

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22 January 2020

Hyuncheol Oh

9

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22 January 2020

Bo Yeon Kim

10

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22 January 2020

Jong Seog Ahn

11

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22 January 2020

publication date

8 February 2012

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The Journal of Antibiotics

22 January 2020

published in

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volume

65

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issue

4

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page(s)

215-217

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https://scigraph.springernature.com/pub.10.1038/ja.2011.141

22 January 2020

exact match

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Indoleamine 2,3-dioxygenase and tumor-induced tolerance

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Oxidation of L-tryptophan in biology: a comparison between tryptophan 2,3-dioxygenase and indoleamine 2,3-dioxygenase.

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Enzyme kinetic and spectroscopic studies of inhibitor and effector interactions with indoleamine 2,3-dioxygenase. 2. Evidence for the existence of another binding site in the enzyme for indole derivative effectors

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Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase

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Indoleamine 2,3 dioxygenase and quinolinic acid immunoreactivity in Alzheimer's disease hippocampus

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Immunohistochemical study on caveolin-1α in regenerating process of tubular cells in gentamicin-induced acute tubular injury in rats

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Inhibition of indoleamine 2,3-dioxygenase (IDO) enhances elimination of virus-infected macrophages in an animal model of HIV-1 encephalitis

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Inhibition of indoleamine 2,3-dioxygenase, an immunoregulatory target of the cancer suppression gene Bin1, potentiates cancer chemotherapy.

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Indoleamine 2,3-dioxygenase in cancer: targeting pathological immune tolerance with small-molecule inhibitors.

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Indoleamine 2,3-dioxygenase in immune suppression and cancer.

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A key in vivo antitumor mechanism of action of natural product-based brassinins is inhibition of indoleamine 2,3-dioxygenase

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Synthesis of indoleamine 2,3-dioxygenase inhibitory analogues of the sponge alkaloid exiguamine A.

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Highlights at the gate of tryptophan catabolism: a review on the mechanisms of activation and regulation of indoleamine 2,3-dioxygenase (IDO), a novel target in cancer disease

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Plectosphaeroic acids A, B, and C, indoleamine 2,3-dioxygenase inhibitors produced in culture by a marine isolate of the fungus Plectosphaerella cucumerina.

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7 January 2021

Benzomalvins, new substance P inhibitors from a Penicillium sp

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7 January 2021

S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase.

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7 January 2021

1-Methyl-DL-tryptophan, beta-(3-benzofuranyl)-DL-alanine (the oxygen analog of tryptophan), and beta-[3-benzo(b)thienyl]-DL-alanine (the sulfur analog of tryptophan) are competitive inhibitors for indoleamine 2,3-dioxygenase

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7 January 2021

Targeting the mechanisms of tumoral immune tolerance with small-molecule inhibitors.

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