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  5. (E/Z)-Xanthohumol

(E/Z)-Xanthohumol is a flavonoid isolated from hopfen.

For research use only. We do not sell to patients.

(E/Z)-Xanthohumol Chemical Structure

(E/Z)-Xanthohumol Chemical Structure

CAS No. : 569-83-5

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Other Forms of (E/Z)-Xanthohumol:

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Description

(E/Z)-Xanthohumol is a flavonoid isolated from hopfen[1].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
11.9 μM
Compound: Xn
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay
[PMID: 30196062]
A549 IC50
30.5 μM
Compound: 8a, Xn
Cytotoxicity against human A549 cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay
[PMID: 25629304]
BGC-823 IC50
7.8 μM
Compound: Xanthohumol
Cytotoxicity against human BGC823 cells assessed as cell growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human BGC823 cells assessed as cell growth inhibition after 72 hrs by MTT assay
[PMID: 29288946]
BV-2 IC50
7.92 μM
Compound: 14
Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by griess assay
Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by griess assay
[PMID: 29154541]
HEK293 IC50
35 μM
Compound: 1
Inhibition of TNF-alpha-induced NF-kappaB activation expressed in human HEK293 cells preincubated for 2 hrs before TNFalpha challenge by leuciferase reporter gene assay
Inhibition of TNF-alpha-induced NF-kappaB activation expressed in human HEK293 cells preincubated for 2 hrs before TNFalpha challenge by leuciferase reporter gene assay
[PMID: 19757857]
HeLa IC50
> 40 μM
Compound: 8a, Xn
Inhibition of TrxR in human HeLa cells assessed as depletion of cellular thiol after 48 hrs
Inhibition of TrxR in human HeLa cells assessed as depletion of cellular thiol after 48 hrs
[PMID: 25629304]
HeLa IC50
40.4 μM
Compound: 8a, Xn
Cytotoxicity against human HeLa cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay
Cytotoxicity against human HeLa cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay
[PMID: 25629304]
HeLa IC50
9.4 μM
Compound: 7
Cytotoxicity against human HeLa cells after 72 hrs by MTT assay
Cytotoxicity against human HeLa cells after 72 hrs by MTT assay
[PMID: 20153559]
HeLa IC50
9.4 μM
Compound: 1, xanthohumol
Cytotoxicity against human HeLa cells by MTT assay
Cytotoxicity against human HeLa cells by MTT assay
[PMID: 18343123]
HeLa IC50
9.4 μM
Compound: 1
Cytotoxicity against human HeLa cells by MTT assay after 72 hrs
Cytotoxicity against human HeLa cells by MTT assay after 72 hrs
[PMID: 18611049]
HepG2 IC50
35 μM
Compound: 8a, Xn
Cytotoxicity against human HepG2 cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay
Cytotoxicity against human HepG2 cells assessed as inhibition of cell proliferation after 72 hrs by MTT assay
[PMID: 25629304]
HMEC-1 IC50
11.4 μM
Compound: Xanthohumol
Antiangiogenic activity in SV-40T transfected human HMEC1 cells assessed as inhibition of cell proliferation after 72 hrs by crystal violet staining
Antiangiogenic activity in SV-40T transfected human HMEC1 cells assessed as inhibition of cell proliferation after 72 hrs by crystal violet staining
[PMID: 23030826]
HMEC-1 IC50
11.4 μM
Compound: Xanthohumol
Antiproliferative activity against human HMEC1 cells after 72 hrs
Antiproliferative activity against human HMEC1 cells after 72 hrs
[PMID: 25128665]
HT-29 IC50
91.31 μM
Compound: 1, Xanthohumol
Antiproliferative activity against human HT-29 cells after 72 hrs by SRB assay
Antiproliferative activity against human HT-29 cells after 72 hrs by SRB assay
[PMID: 23466227]
HT-29 IC50
91.31 μM
Compound: 1
Cytotoxicity against human HT-29 cells after 72 hrs by SRB assay
Cytotoxicity against human HT-29 cells after 72 hrs by SRB assay
[PMID: 23434138]
Ishikawa IC50
4.2 μM
Compound: XH
Cytotoxicity against human Ishikawa cells after 96 hrs by SRB assay
Cytotoxicity against human Ishikawa cells after 96 hrs by SRB assay
[PMID: 28812892]
MCF7 IC50
10.95 μM
Compound: 1, Xanthohumol
Antiproliferative activity against human MCF7 cells after 72 hrs by SRB assay
Antiproliferative activity against human MCF7 cells after 72 hrs by SRB assay
[PMID: 23466227]
MCF7 IC50
10.95 μM
Compound: 1
Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay
Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay
[PMID: 23434138]
MCF7 IC50
13.3 μM
Compound: Xanthohumol
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 2 days by SRB assay
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 2 days by SRB assay
[PMID: 33257172]
MCF7 IC50
3.47 μM
Compound: Xanthohumol
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 4 days by SRB assay
Antiproliferative activity against human MCF7 cells assessed as inhibition of cell growth incubated for 4 days by SRB assay
[PMID: 33257172]
NCI-H1975 IC50
13 μM
Compound: Xn
Antiproliferative activity against human NCI-H1975 cells after 72 hrs by MTT assay
Antiproliferative activity against human NCI-H1975 cells after 72 hrs by MTT assay
[PMID: 30196062]
NCI-H460 IC50
6.9 μM
Compound: Xanthohumol
Cytotoxicity against human NCI-H460 cells assessed as cell growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human NCI-H460 cells assessed as cell growth inhibition after 72 hrs by MTT assay
[PMID: 29288946]
NCI-H460 IC50
7.5 μM
Compound: Xn
Antiproliferative activity against human NCI-H460 cells after 72 hrs by MTT assay
Antiproliferative activity against human NCI-H460 cells after 72 hrs by MTT assay
[PMID: 30196062]
PC-3 IC50
10.67 μM
Compound: 1, Xanthohumol
Antiproliferative activity against human PC3 cells after 72 hrs by SRB assay
Antiproliferative activity against human PC3 cells after 72 hrs by SRB assay
[PMID: 23466227]
PC-3 IC50
10.67 μM
Compound: 1
Cytotoxicity against human PC3 cells after 72 hrs by SRB assay
Cytotoxicity against human PC3 cells after 72 hrs by SRB assay
[PMID: 23434138]
RAW264.7 IC50
8.3 μM
Compound: 1
Inhibition of LPS/IFN-gamma-induced NO production in mouse RAW264.7 cells after 16 hrs
Inhibition of LPS/IFN-gamma-induced NO production in mouse RAW264.7 cells after 16 hrs
[PMID: 15679315]
SGC-7901 IC50
10 μM
Compound: Xanthohumol
Cytotoxicity against human SGC7901 cells assessed as cell growth inhibition after 72 hrs by MTT assay
Cytotoxicity against human SGC7901 cells assessed as cell growth inhibition after 72 hrs by MTT assay
[PMID: 29288946]
VSMC IC50
3.49 μM
Compound: 1
Inhibition of PDGF-BB-induced rat VSMC proliferation preincubated for 30 mins followed by PDGF-BB addition measured after 48 hrs by resazurin assay
Inhibition of PDGF-BB-induced rat VSMC proliferation preincubated for 30 mins followed by PDGF-BB addition measured after 48 hrs by resazurin assay
[PMID: 28627872]
Molecular Weight

354.40

Formula

C21H22O5

CAS No.
SMILES

O=C(C1=C(OC)C=C(O)C(C/C=C(C)\C)=C1O)/C=C/C2=CC=C(O)C=C2

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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(E/Z)-Xanthohumol
Cat. No.:
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