ChemicalBook >> CAS DataBase List >>OPHIOBOLIN A

OPHIOBOLIN A

CAS No.
4611-05-6
Chemical Name:
OPHIOBOLIN A
Synonyms
ophiobolin;cochliobolin;OPHIOBOLIN A;COCHLIOBOLIN A;Ophiobolin A >=95% (HPLC);Ophiobolin A (Cochliobolin A);Ophiobolin, Helminthosporium sp.;Cochliobolin A, Ophiobolin, Ophiobalin;ophiobolin A from helminthosporium sp.;18-epoxy-3-hydroxy-5-oxo-19-dien-25-a(18r)-ophiobola-14
CBNumber:
CB2735485
Molecular Formula:
C25H36O4
Molecular Weight:
400.55
MDL Number:
MFCD32182611
MOL File:
4611-05-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08
Product description Number Pack Size Price
Ophiobolin A ≥95% (HPLC) SML1478 100μG $103
Ophiobolin A ≥95% (HPLC) SML1478 1MG $406
Ophiobolin A ≥95% 15381 1mg $303
Ophiobolin A ≥95% 15381 5mg $902
Ophiobolin A ≥95% 15381 1mg $275
More product size

OPHIOBOLIN A Properties

Melting point 182°C
Boiling point 443.19°C (rough estimate)
Density 1.0278 (rough estimate)
refractive index 1.4460 (estimate)
storage temp. 2-8°C
solubility Soluble in DMSO (up to 10 mg/ml)
form White to off-white solid.
pka 13.84±0.70(Predicted)
color White
biological source (from Biopolaris leersia fungal metabolite)
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.
InChIKey MWYYLZRWWNBROW-BDZRSQQBSA-N
SMILES [H]C(/C1=C/C[C@]([C@]2(O[C@@H](C=C(C)C)C[C@@H]2C)CC3)([H])[C@@]3(C)C[C@@]([C@](C)(O)C4)([H])[C@]1([H])C4=O)=O
UNSPSC Code 12352200
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310-P405-P501
Hazard Codes  Xn
Risk Statements  20/21/22
Safety Statements  36
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  RL1576000
HS Code  2932190090
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Toxicity mouse,LD50,intraperitoneal,21mg/kg (21mg/kg),"CRC Handbook of Antibiotic Compounds," Vols.1- , Berdy, J., Boca Raton, FL, CRC Press, 1980Vol. 6, Pg. 143, 1981.
NFPA 704
0
3 0

OPHIOBOLIN A price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML1478 Ophiobolin A ≥95% (HPLC) 4611-05-6 100μG $103 2026-04-30 Buy
Sigma-Aldrich SML1478 Ophiobolin A ≥95% (HPLC) 4611-05-6 1MG $406 2026-04-30 Buy
Cayman Chemical 15381 Ophiobolin A ≥95% 4611-05-6 1mg $303 2026-04-30 Buy
Cayman Chemical 15381 Ophiobolin A ≥95% 4611-05-6 5mg $902 2026-04-30 Buy
Cayman Chemical 15381 Ophiobolin A ≥95% 4611-05-6 1mg $275 2024-03-01 Buy
Product number Packaging Price Buy
SML1478 100μG $103 Buy
SML1478 1MG $406 Buy
15381 1mg $303 Buy
15381 5mg $902 Buy
15381 1mg $275 Buy

OPHIOBOLIN A Chemical Properties,Uses,Production

Description

Ophiobolin A (4611-05-6) selectively inhibits the growth of cancer cells (IC50=0.4-4.3 μM) over normal cells (IC50=20.9 μM).1 Induces non-apoptotic cell death in glioblastoma cells and is active in an in vivo model.2 Covalently reacts with primary amines such as lysine side chains2 and phosphatidylethanolamine3 forming unique pyrrole adducts. Induces ER stress4, paraptosis4 and autophagy5.

Uses

Ophiobolin A is the dominant member of a class of phytotoxic metabolites produced by plant pathogenic fungi. Ophiobolin A acts by inhibiting calmodulin action in calcium regulation.

Definition

ChEBI: A sesterterpenoid that is ophiobolane with a hydroxy group at position 3, oxo groups at positions 5 and 25, double bonds at positions 7-8 and 19-20, and an oxygen link between positions 14 and 18.

References

[1] DIMPLE R. BHATIA . Anticancer activity of Ophiobolin A, isolated from the endophytic fungus Bipolaris setariae[J]. Natural Product Research, 2016, 30 12: Pages 1455-1458. DOI:10.1080/14786419.2015.1062760
[2] RAMESH DASARI . Fungal metabolite ophiobolin A as a promising anti-glioma agent: In vivo evaluation, structure–activity relationship and unique pyrrolylation of primary amines[J]. Bioorganic & Medicinal Chemistry Letters, 2015, 25 20: Pages 4544-4548. DOI:10.1016/j.bmcl.2015.08.066
[3] CHRISTOPHER CHIDLEY. The anticancer natural product ophiobolin A induces cytotoxicity by covalent modification of phosphatidylethanolamine.[J]. eLife, 2016. DOI:10.7554/elife.14601
[4] IN YOUNG KIM. Ophiobolin A kills human glioblastoma cells by inducing endoplasmic reticulum stress via disruption of thiol proteostasis.[J]. Oncotarget, 2017, 8 63: 106740-106752. DOI:10.18632/oncotarget.22537
[5] C. RODOLFO. Ophiobolin A Induces Autophagy and Activates the Mitochondrial Pathway of Apoptosis in Human Melanoma Cells[J]. PLoS ONE, 2016, 11 1. DOI:10.1371/journal.pone.0167672

OPHIOBOLIN A Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 56)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32466 58
BOC Sciences
16314854226; +16314854226 inquiry@bocsci.com United States 19853 58
Aladdin Scientific
tp@aladdinsci.com United States 57505 58
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29975 65
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9804 58
Shanghai YuanYe Biotechnology Co., Ltd. 13636370518 shyysw007@163.com China 89686 60
Lynnchem 86-(0)29-85992781 17792393971 info@lynnchem.com China 4587 58
Novachemistry 44-20819178-90 02081917890 info@novachemistry.com United Kingdom 4381 58
Shenzhen Regent Biochemical Technology Co., Ltd. 0755-85201366 18938635012 sales@regentsciences.com China 9361 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 +86-13028896684; sales@rrkchem.com China 57422 58

View Lastest Price from OPHIOBOLIN A manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ophiobolin A pictures 2026-07-16 Ophiobolin A
4611-05-6
$688.00 10g TargetMol Chemicals Inc.
Ophiobolin A pictures 2025-12-22 Ophiobolin A
4611-05-6
$997.00 10g TargetMol Chemicals Inc.
18-epoxy-3-hydroxy-5-oxo-19-dien-25-a(18r)-ophiobola-14 cochliobolin ophiobolin COCHLIOBOLIN A ophiobolin A from helminthosporium sp. Ophiobolin, Helminthosporium sp. (18R)-14,18-Epoxy-3-hydroxy-5-oxoophiobola-7,19-dien-25-al (18R)-3-Hydroxy-5-oxo-14,18-epoxyophiobola-7,19-diene-25-al Cochliobolin A, Ophiobolin, Ophiobalin OPHIOBOLIN A Spiro[dicyclopenta[a,d]cyclooctene-3(2H),2'(3'H)-furan]-6-carboxaldehyde, 1,3a,4,4',5',6a,7,8,9,9a,10,10a-dodecahydro-9-hydroxy-3',9,10a-trimethyl-5'-(2-methyl-1-propen-1-yl)-7-oxo-, (2'S,3'S,3aR,5'R,6aS,9R,9aS,10aR)- Ophiobolin A >=95% (HPLC) Ophiobolin A (Cochliobolin A) 4611-05-6 C25H36O4 Cell Signaling and Neuroscience Calcium Antagonists Cell Biology BioChemical Intracellular Calcium Signaling