1. Apoptosis Autophagy Metabolic Enzyme/Protease Immunology/Inflammation NF-κB Cell Cycle/DNA Damage
  2. Apoptosis Autophagy Reactive Oxygen Species (ROS) CDK
  3. Fascaplysin

Fascaplysin is an antimicrobial and cytotoxic red pigment, that can come from the marine sponge (Fascaplysinopsis sp.). Fascaplysin has been synthesized in seven steps from indole (65% yield). Fascaplysin can induces apoptosis and autophagy in human leukemia HL-60 cells. Fascaplysin shows anti-tumor activity.

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Fascaplysin

Fascaplysin Chemical Structure

CAS No. : 114719-57-2

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Customer Review

Based on 1 publication(s) in Google Scholar

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  • Biological Activity

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Description

Fascaplysin is an antimicrobial and cytotoxic red pigment, that can come from the marine sponge (Fascaplysinopsis sp.). Fascaplysin has been synthesized in seven steps from indole (65% yield). Fascaplysin can induces apoptosis and autophagy in human leukemia HL-60 cells. Fascaplysin shows anti-tumor activity[1][2].

IC50 & Target

CDK4

 

Cellular Effect
Cell Line Type Value Description References
786-0 IC50
6.7 μM
Compound: 1, NSC-622398
Antitumor activity against human 786-O cells
Antitumor activity against human 786-O cells
[PMID: 15165138]
A498 IC50
5.2 μM
Compound: 1, NSC-622398
Antitumor activity against human A498 cells
Antitumor activity against human A498 cells
[PMID: 15165138]
A549 IC50
0.69 μM
Compound: 2
Growth inhibition of p53+, pRb+ human A549 cells after 48 hrs by MTT assay
Growth inhibition of p53+, pRb+ human A549 cells after 48 hrs by MTT assay
[PMID: 25368960]
A549 IC50
4.2 μM
Compound: 1, NSC-622398
Antitumor activity against human A549/ATCC cells
Antitumor activity against human A549/ATCC cells
[PMID: 15165138]
ACHN IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human ACHN cells
Antitumor activity against human ACHN cells
[PMID: 15165138]
BT-549 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human BT549 cells
Antitumor activity against human BT549 cells
[PMID: 15165138]
CAKI-1 IC50
6.1 μM
Compound: 1, NSC-622398
Antitumor activity against human Caki1 cells
Antitumor activity against human Caki1 cells
[PMID: 15165138]
CCRF-CEM IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human CCRF-CEM cells
Antitumor activity against human CCRF-CEM cells
[PMID: 15165138]
COLO 205 IC50
1.2 μM
Compound: 1, NSC-622398
Antitumor activity against human COLO205 cells
Antitumor activity against human COLO205 cells
[PMID: 15165138]
Calu-1 IC50
1.3 μM
Compound: 2
Growth inhibition of p53 null, pRb+ human Calu1 cells after 48 hrs by MTT assay
Growth inhibition of p53 null, pRb+ human Calu1 cells after 48 hrs by MTT assay
[PMID: 25368960]
DU-145 IC50
4.9 μM
Compound: 1, NSC-622398
Antitumor activity against human DU145 cells
Antitumor activity against human DU145 cells
[PMID: 15165138]
EKVX IC50
5.1 μM
Compound: 1, NSC-622398
Antitumor activity against human EKVX cells
Antitumor activity against human EKVX cells
[PMID: 15165138]
HCC 2998 IC50
1.7 μM
Compound: 1, NSC-622398
Antitumor activity against human HCC2998 cells
Antitumor activity against human HCC2998 cells
[PMID: 15165138]
HCT-116 IC50
0.6 μM
Compound: 1, NSC-622398
Antitumor activity against human HCT116 cells
Antitumor activity against human HCT116 cells
[PMID: 15165138]
HCT-15 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human HCT15 cells
Antitumor activity against human HCT15 cells
[PMID: 15165138]
HL-60(TB) IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human HL-60(TB) cells
Antitumor activity against human HL-60(TB) cells
[PMID: 15165138]
HOP-62 IC50
4.7 μM
Compound: 1, NSC-622398
Antitumor activity against human HOP62 cells
Antitumor activity against human HOP62 cells
[PMID: 15165138]
HT-29 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human HT-29 cells
Antitumor activity against human HT-29 cells
[PMID: 15165138]
Hs-578T IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human Hs 578T cells
Antitumor activity against human Hs 578T cells
[PMID: 15165138]
Huh-7 CC50
0.589 μM
Compound: GNF-Pf-1458
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
[PMID: 18579783]
IGROV-1 IC50
4.5 μM
Compound: 1, NSC-622398
Antitumor activity against human IGROV1 cells
Antitumor activity against human IGROV1 cells
[PMID: 15165138]
K562 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human K562 cells
Antitumor activity against human K562 cells
[PMID: 15165138]
KM12 IC50
4.6 μM
Compound: 1, NSC-622398
Antitumor activity against human KM12 cells
Antitumor activity against human KM12 cells
[PMID: 15165138]
LOX IMVI IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human LOXIMVI cells
Antitumor activity against human LOXIMVI cells
[PMID: 15165138]
LS174T IC50
0.88 μM
Compound: 2
Growth inhibition of p53+, pRb+ human LS 174T cells after 48 hrs by MTT assay
Growth inhibition of p53+, pRb+ human LS 174T cells after 48 hrs by MTT assay
[PMID: 25368960]
M14 IC50
0.92 μM
Compound: 1, NSC-622398
Antitumor activity against human M14 cells
Antitumor activity against human M14 cells
[PMID: 15165138]
MCF7 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against ADF-resistant human MCF7 cells
Antitumor activity against ADF-resistant human MCF7 cells
[PMID: 15165138]
MCF7 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human MCF7 cells
Antitumor activity against human MCF7 cells
[PMID: 15165138]
MDA-MB-231 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human MDA-MB-231 cells
Antitumor activity against human MDA-MB-231 cells
[PMID: 15165138]
MDA-MB-435 IC50
0.56 μM
Compound: 1, NSC-622398
Antitumor activity against human MDA-MB-435 cells
Antitumor activity against human MDA-MB-435 cells
[PMID: 15165138]
MDA-N IC50
0.56 μM
Compound: 1, NSC-622398
Antitumor activity against human MDA-N cells
Antitumor activity against human MDA-N cells
[PMID: 15165138]
MOLT-4 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human MOLT4 cells
Antitumor activity against human MOLT4 cells
[PMID: 15165138]
Malme-3M IC50
0.36 μM
Compound: 1, NSC-622398
Antitumor activity against human MALME-3M cells
Antitumor activity against human MALME-3M cells
[PMID: 15165138]
NCI-H226 IC50
9.6 μM
Compound: 1, NSC-622398
Antitumor activity against human NCI-H226 cells
Antitumor activity against human NCI-H226 cells
[PMID: 15165138]
NCI-H23 IC50
4.5 μM
Compound: 1, NSC-622398
Antitumor activity against human NCI-H23 cells
Antitumor activity against human NCI-H23 cells
[PMID: 15165138]
NCI-H322M IC50
5 μM
Compound: 1, NSC-622398
Antitumor activity against human NCI-H322M cells
Antitumor activity against human NCI-H322M cells
[PMID: 15165138]
NCI-H460 IC50
4.2 μM
Compound: 1, NSC-622398
Antitumor activity against human NCI-H460 cells
Antitumor activity against human NCI-H460 cells
[PMID: 15165138]
NCI-H522 IC50
4.5 μM
Compound: 1, NSC-622398
Antitumor activity against human NCI-H522 cells
Antitumor activity against human NCI-H522 cells
[PMID: 15165138]
OVCAR-3 IC50
1.5 μM
Compound: 1, NSC-622398
Antitumor activity against human OVCAR-3 cells
Antitumor activity against human OVCAR-3 cells
[PMID: 15165138]
OVCAR-4 IC50
5.3 μM
Compound: 1, NSC-622398
Antitumor activity against human OVCAR4 cells
Antitumor activity against human OVCAR4 cells
[PMID: 15165138]
OVCAR-5 IC50
4.4 μM
Compound: 1, NSC-622398
Antitumor activity against human OVCAR5 cells
Antitumor activity against human OVCAR5 cells
[PMID: 15165138]
OVCAR-8 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human OVCAR8 cells
Antitumor activity against human OVCAR8 cells
[PMID: 15165138]
PC-3 IC50
0.92 μM
Compound: 2
Growth inhibition of p53 null,pRb+ human PC3 cells after 48 hrs by MTT assay
Growth inhibition of p53 null,pRb+ human PC3 cells after 48 hrs by MTT assay
[PMID: 25368960]
PC-3 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human PC3 cells
Antitumor activity against human PC3 cells
[PMID: 15165138]
RPMI-8226 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human RPMI8226 cells
Antitumor activity against human RPMI8226 cells
[PMID: 15165138]
RXF 393 IC50
3.5 μM
Compound: 1, NSC-622398
Antitumor activity against human RXF393 cells
Antitumor activity against human RXF393 cells
[PMID: 15165138]
SF-268 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human SF268 cells
Antitumor activity against human SF268 cells
[PMID: 15165138]
SF-295 IC50
3.9 μM
Compound: 1, NSC-622398
Antitumor activity against human SF295 cells
Antitumor activity against human SF295 cells
[PMID: 15165138]
SF-539 IC50
4.2 μM
Compound: 1, NSC-622398
Antitumor activity against human SF539 cells
Antitumor activity against human SF539 cells
[PMID: 15165138]
SK-MEL-28 IC50
9.3 μM
Compound: 1, NSC-622398
Antitumor activity against human SK-MEL-28 cells
Antitumor activity against human SK-MEL-28 cells
[PMID: 15165138]
SK-MEL-5 IC50
2 μM
Compound: 1, NSC-622398
Antitumor activity against human SK-MEL-5 cells
Antitumor activity against human SK-MEL-5 cells
[PMID: 15165138]
SK-OV-3 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human SKOV3 cells
Antitumor activity against human SKOV3 cells
[PMID: 15165138]
SN12C IC50
4.2 μM
Compound: 1, NSC-622398
Antitumor activity against human SN12C cells
Antitumor activity against human SN12C cells
[PMID: 15165138]
SNB-19 IC50
6.1 μM
Compound: 1, NSC-622398
Antitumor activity against human SNB19 cells
Antitumor activity against human SNB19 cells
[PMID: 15165138]
SNB-75 IC50
5.4 μM
Compound: 1, NSC-622398
Antitumor activity against human SNB75 cells
Antitumor activity against human SNB75 cells
[PMID: 15165138]
SR IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human SR cells
Antitumor activity against human SR cells
[PMID: 15165138]
SW-620 IC50
3.7 μM
Compound: 1, NSC-622398
Antitumor activity against human SW620 cells
Antitumor activity against human SW620 cells
[PMID: 15165138]
Sf9 IC50
0.35 μM
Compound: Fascaplysin
Inhibition of CDK4/Cyclin D (unknown origin) expressed in baculovirus infected insect Sf9 cells using human pRB as substrate in presence of [gamma-32P]ATP
Inhibition of CDK4/Cyclin D (unknown origin) expressed in baculovirus infected insect Sf9 cells using human pRB as substrate in presence of [gamma-32P]ATP
[PMID: 26741853]
Sf9 IC50
0.55 μM
Compound: 1
Inhibition of human CDK4/GST-cyclin D1 expressed in Sf9 cells assessed as retinoblastoma GST-RB152 phosphorylation
Inhibition of human CDK4/GST-cyclin D1 expressed in Sf9 cells assessed as retinoblastoma GST-RB152 phosphorylation
[PMID: 18650093]
Sf9 IC50
0.55 μM
Compound: 4
Inhibition of human CDK4/ Cyclin D1 catalytic subunit expressed in Sf9 insect cells assessed as GST-RB152 fusion protein phosphorylation-associated depletion in ATP level by luminescence assay
Inhibition of human CDK4/ Cyclin D1 catalytic subunit expressed in Sf9 insect cells assessed as GST-RB152 fusion protein phosphorylation-associated depletion in ATP level by luminescence assay
[PMID: 19632122]
Sf9 IC50
500 μM
Compound: 1
Inhibition of human CDK2/GST-cyclin A expressed in Sf9 cells assessed as histone phosphorylation
Inhibition of human CDK2/GST-cyclin A expressed in Sf9 cells assessed as histone phosphorylation
[PMID: 18650093]
Sf9 IC50
500 μM
Compound: 4
Inhibition of human CDK2/ Cyclin A catalytic subunit expressed in Sf9 insect cells assessed as histone H1 phosphorylation-associated depletion in ATP level by luminescence assay
Inhibition of human CDK2/ Cyclin A catalytic subunit expressed in Sf9 insect cells assessed as histone H1 phosphorylation-associated depletion in ATP level by luminescence assay
[PMID: 19632122]
T47D IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human T47D cells
Antitumor activity against human T47D cells
[PMID: 15165138]
TK-10 IC50
5.4 μM
Compound: 1, NSC-622398
Antitumor activity against human TK10 cells
Antitumor activity against human TK10 cells
[PMID: 15165138]
U-251 IC50
3.6 μM
Compound: 1, NSC-622398
Antitumor activity against human U251 cells
Antitumor activity against human U251 cells
[PMID: 15165138]
UACC-257 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human UACC257 cells
Antitumor activity against human UACC257 cells
[PMID: 15165138]
UACC-62 IC50
4.9 μM
Compound: 1, NSC-622398
Antitumor activity against human UACC62 cells
Antitumor activity against human UACC62 cells
[PMID: 15165138]
UO-31 IC50
> 10 μM
Compound: 1, NSC-622398
Antitumor activity against human UO31 cells
Antitumor activity against human UO31 cells
[PMID: 15165138]
In Vitro

Fascaplysin induces autophagy as a cytoprotective response via ROS and p8 in vascular endothelial cells (VECs)[2].
Fascaplysin targets metabolic activity of the prostate cancer cells, without disrupting cell membrane's integrity[2].
. Fascaplysin induces caspase mediated crosstalk between apoptosis and autophagy through the inhibition of PI3K/AKT/mTOR signaling cascade in human leukemia HL-60 cells[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Fascaplysin suppresses the growth of S180 cell-implanted tumors in vivo[2]

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

306.75

Formula

C18H11ClN2O

CAS No.
Appearance

Solid

Color

Light yellow to brown

SMILES

O=C1C2=C3NC4=C(C=CC=C4)C3=CC=[N+]2C5=C1C=CC=C5.[Cl-]

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Purity & Documentation

Purity: 95.64%

References
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Product Name:
Fascaplysin
Cat. No.:
HY-112328
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