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JASPLAKINOLIDE

CAS No.
102396-24-7
Chemical Name:
JASPLAKINOLIDE
Synonyms
NSC 613009;JASPLAKINOLIDE;GQWYWHOHRVVHAP-DHKPLNAMSA-N;JASPLAKINOLIDE, JASPIS JOHNSTONI;Jasplakinolide, Actin polymerization and stabilization inducer;Jasplakinolide, Jaspis johnstoni - CAS 102396-24-7 - Calbiochem;Cyclo[(3R)-3-(4-hydroxyphenyl)-β-alanyl-(2S,4E,6R,8S)-8-hydroxy-2,4,6-trimethyl-4-nonenoyl-L-alanyl-2-bromo-N-methyl-D-tryptophyl];(3S,6R,9R,13S,15R,16E,19S)-3,5,13,15,17,19-Hexamethyl-6-[(2-bromo-1H-indole-3-yl)methyl]-9-(4-hydroxyphenyl)-12-oxa-2,5,8-triazacyclononadeca-16-ene-1,4,7,11-tetraone;[3S,6R,9R,13S,15R,19S,16E,(+)]-6-[(2-Bromo-1H-indol-3-yl)methyl]-9-(4-hydroxyphenyl)-3,5,13,15,17,19-hexamethyl-2,5,8-triaza-12-oxacyclononadecan-16-ene-1,4,7,11-tetrone
CBNumber:
CB0703307
Molecular Formula:
C36H45BrN4O6
Molecular Weight:
709.67
MDL Number:
MFCD00873735
MOL File:
102396-24-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08

JASPLAKINOLIDE Properties

Melting point 110℃ (decomposition)
storage temp. -20°C
solubility DMSO: >2mg/mL
form Off-white solid
color off white to beige
InChIKey GQWYWHOHRVVHAP-DHKPLNAMSA-N
SMILES C[C@H]1C[C@@H](C)\C=C(C)\C[C@H](C)C(=O)N[C@@H](C)C(=O)N(C)[C@H](Cc2c(Br)[nH]c3ccccc23)C(=O)N[C@H](CC(=O)O1)c4ccc(O)cc4
UNSPSC Code 12352200
NACRES NA.77

SAFETY

Risk and Safety Statements

Hazard statements  H413
Precautionary statements  P273-P501
RIDADR  3172
WGK Germany  3
RTECS  GX7000000
HazardClass  6.1(b)
PackingGroup  III
Storage Class 11 - Combustible Solids

JASPLAKINOLIDE price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich J4580 Jasplakinolide ≥97% (HPLC) 102396-24-7 100μg $815 2026-04-30 Buy
Sigma-Aldrich 420107-M Jasplakinolide, Jaspis johnstoni A cell-permeable F-actin probe. 102396-24-7 50 μg $299 2026-04-30 Buy
Sigma-Aldrich 420107-M Jasplakinolide, Jaspis johnstoni A cell-permeable F-actin probe. 102396-24-7 1 unit $195.3 2025-07-31 Buy
Cayman Chemical 11705 Jasplakinolide ≥95% 102396-24-7 50μg $237 2026-04-30 Buy
Cayman Chemical 11705 Jasplakinolide ≥98% 102396-24-7 100μg $287 2024-03-01 Buy
Product number Packaging Price Buy
J4580 100μg $815 Buy
420107-M 50 μg $299 Buy
420107-M 1 unit $195.3 Buy
11705 50μg $237 Buy
11705 100μg $287 Buy

JASPLAKINOLIDE Chemical Properties,Uses,Production

Description

Jasplakinolide is a natural macrocyclic peptide first isolated from a marine sponge. It potently inhibits the proliferation of PC3 prostate carcinoma cells (IC50 = 35 nM) by binding F-actin (KD = 15 nM). This binding of jasplakinolide to actin, which is competitive with phalloidin, stabilizes actin filaments in vitro but disrupts actin filaments and induces irregular polymerization of monomeric actin in vivo. This compound is used to investigate the role of actin in diverse cellular roles, such as motility, transport, and development.

Uses

Jasplakinolide is a potent inhibitor of prostrate and breast carcinoma cell proliferation. Also acts as an actin stabilizing agent, affecting chromosome movement in studies.

Uses

Jasplakinolide is a natural macrocyclic peptide first isolated from a marine sponge. It potently inhibits the proliferation of PC3 prostate carcinoma cells (IC50 = 35 nM) by binding F-actin (KD = 15 nM). This binding of jasplakinolide to actin, which is competitive with phalloidin, stabilizes actin filaments in vitro but disrupts actin filaments and induces irregular polymerization of monomeric actin in vivo. This compound is used to investigate the role of actin in diverse cellular roles, such as motility, transport, and development.

Uses

Jasplakinolide has been used to analyze its influence on sciatic nerve guidance effect in vivo in chicken embryos. It has also been used to apply on the control cells for the treatment for blocking actin dynamics.

Definition

ChEBI: A cyclodepsipeptide isolated from Jaspis splendens and has been shown to exhibit antineoplastic activity.

Biochem/physiol Actions

Jasplakinolide is an actin-specific reagent that promotes actin polymerization and stabilizes actin filaments. In vitro, Jasplakinolidet potently induces actin polymerization by stimulating actin filament nucleation and competes with phalloidin for actin binding (Kd = 15 nM). In vivo, Jasplakinolide has been found to disrupt actin filaments and induce polymerization of monomeric actin into amorphous masses, the exact mechanism of which has not been determined yet. Jasplakinolide differs from other actin stabilizers in that it is cell permeable. This peptide has fungicidal, insecticidal and antiproliferative activity, and is useful for investigating cell processes mediated by actin polymerization and depolymerization, such as cell adhesion, locomotion, endocytosis, and vesicle sorting and release.

storage

+4°C

References

[1] M R BUBB. Jasplakinolide, a cytotoxic natural product, induces actin polymerization and competitively inhibits the binding of phalloidin to F-actin.[J]. The Journal of Biological Chemistry, 1994, 269 21: 14869-14871.
[2] M R BUBB. Effects of jasplakinolide on the kinetics of actin polymerization. An explanation for certain in vivo observations.[J]. The Journal of Biological Chemistry, 2000, 275 7: 5163-5170. DOI: 10.1074/jbc.275.7.5163
[3] DAVID VAN GOOR. The role of actin turnover in retrograde actin network flow in neuronal growth cones.[J]. PLoS ONE, 2012: e30959. DOI: 10.1371/journal.pone.0030959
[4] XIAOYUN ZHANG. Actin stabilization by jasplakinolide affects the function of bone marrow-derived late endothelial progenitor cells.[J]. PLoS ONE, 2012: e50899. DOI: 10.1371/journal.pone.0050899
[5] TANJA EISEMANN. An advanced glioma cell invasion assay based on organotypic brain slice cultures.[J]. BMC Cancer, 2018: 103. DOI: 10.1186/s12885-018-4007-4

JASPLAKINOLIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 67)Suppliers
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 9920 65
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29985 65
Shanghai Tauto Biotech Co., Ltd. 021-51320588 tauto@tautobiotech.com China 3984 66
Shanghai TaoSu Biochemical Technology Co., Ltd. 021-33632979 info@tsbiochem.com China 8039 58
Quality Control Solutions Ltd. 0755-66853366 13670046396 orders@qcsrm.com China 18188 56
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8435 60
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58

View Lastest Price from JASPLAKINOLIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Jasplakinolide pictures 2026-07-15 Jasplakinolide
102396-24-7
$998.00 10g TargetMol Chemicals Inc.
JASPLAKINOLIDE Jasplakinolide, Jaspis johnstoni - CAS 102396-24-7 - Calbiochem Cyclo[(3R)-3-(4-hydroxyphenyl)-β-alanyl-(2S,4E,6R,8S)-8-hydroxy-2,4,6-trimethyl-4-nonenoyl-L-alanyl-2-bromo-N-methyl-D-tryptophyl] JASPLAKINOLIDE, JASPIS JOHNSTONI (3S,6R,9R,13S,15R,16E,19S)-3,5,13,15,17,19-Hexamethyl-6-[(2-bromo-1H-indole-3-yl)methyl]-9-(4-hydroxyphenyl)-12-oxa-2,5,8-triazacyclononadeca-16-ene-1,4,7,11-tetraone [3S,6R,9R,13S,15R,19S,16E,(+)]-6-[(2-Bromo-1H-indol-3-yl)methyl]-9-(4-hydroxyphenyl)-3,5,13,15,17,19-hexamethyl-2,5,8-triaza-12-oxacyclononadecan-16-ene-1,4,7,11-tetrone NSC 613009 GQWYWHOHRVVHAP-DHKPLNAMSA-N Jasplakinolide, Actin polymerization and stabilization inducer 102396-24-7 Amines, Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals