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APHIDICOLIN

CAS No.
38966-21-1
Chemical Name:
APHIDICOLIN
Synonyms
APC;ici69653;nsc-234714;APHIDICOLIN;(+)-APHIDICOLIN;,11a-beta,11b-beta))-;APHIDICOLIN USP/EP/BP;Aphidicolin, Ready Made Solution;(+)-APHIDICOLIN, NIGROSPORA ORYZAE;Aphidicolin, froM Nigrospora oryzae
CBNumber:
CB6683304
Molecular Formula:
C20H34O4
Molecular Weight:
338.48
MDL Number:
MFCD00083214
MOL File:
38966-21-1.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

APHIDICOLIN Properties

Melting point 218-220°C
alpha D27 +12° (c = 1 in methanol)
Boiling point 394.61°C (rough estimate)
Density 1.0057 (rough estimate)
vapor pressure 0.55 hPa ( 20 °C)
refractive index 1.4434 (estimate)
Flash point 87℃
storage temp. 2-8°C
solubility ethanol: soluble1mg/mL (stable at least a week at 4°C.)
form White solid
pka 14.24±0.70(Predicted)
color colorless
optical activity [α]27/D +12°, c = 1 in methanol(lit.)
Water Solubility Soluble in DMSO or methanol. Insoluble in water. Store solutions at -20°
Merck 13,734
BRN 4689958
Stability Stable for 2 years from date of purchase from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
FDA UNII 192TJ6PP19

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P271-P280
Safety Statements  22-24
RIDADR  NA 1993 / PGIII
WGK Germany  3
RTECS  PB9185000
10-21
HS Code  29419090
NFPA 704
0
2 0

APHIDICOLIN price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 89458 Aphidicolin analytical standard 38966-21-1 5mg $1120 2024-03-01 Buy
Sigma-Aldrich 5.04744 InSolution Aphidicolin - CAS 38966-21-1 - Calbiochem 38966-21-1 1mg $167 2024-03-01 Buy
Sigma-Aldrich 178273 Aphidicolin 38966-21-1 1mg $144 2024-03-01 Buy
Alfa Aesar J60236 Aphidicolin 38966-21-1 1mg $207 2023-06-20 Buy
Alfa Aesar J60236 Aphidicolin 38966-21-1 5mg $607 2023-06-20 Buy
Product number Packaging Price Buy
89458 5mg $1120 Buy
5.04744 1mg $167 Buy
178273 1mg $144 Buy
J60236 1mg $207 Buy
J60236 5mg $607 Buy

APHIDICOLIN Chemical Properties,Uses,Production

Description

(+)-Aphidicolin is a natural tetracyclic diterpene first isolated from the fungus C. aphidicola and shown to have antiviral activity against herpes simplex. In eukaryotic cells, it is a cell-permeable, reversible inhibitor of DNA replication, specifically blocking the activity of DNA polymerases α, δ, and ε when used at low micromolar levels. Aphidicolin can be used, at 3 μM, to arrest cells in G1/S phase or to increase gene amplification frequency.

Chemical Properties

White crystal

Uses

A DNA polymerase inhibitor. Blocks the cell cycle at the early S-phase

Uses

Aphidicolin is a tetracyclic diterpene antibiotic isolated from fungi, notably Cephalosporium, Nigrospora, Harziella and Phoma. Aphidicolin has antibiotic, antiviral and antimitotic properties, blocking the cell cycle at early S-phase. This property has been used to synchronise cell division and is useful as a tool in cell differentiation research. Aphidicolin is a reversible inhibitor of DNA replication by inhibiting selected DNA polymerases. Aphidicolin induces apoptosis, prolongs the half-life of DNA methyltransferase, is active against Leishmania parasites and acts synergistically with the antitumour agents, vincristine and doxorubicin.

Uses

(+)-Aphidicolin is a naturally occurring tetracyclic diterpene with potential antiviral and antimitotical properties.

Definition

ChEBI: A tetracyclic diterpenoid that has an tetradecahydro-8,11a-methanocyclohepta[a]naphthalene skeleton with two hydroxymethyl substituents at positions 4 and 9, two methyl substituents at positions 4 and 11b and two hydroxy substituents at positi ns 3 and 9. An antibiotic with antiviral and antimitotical properties. Aphidicolin is a reversible inhibitor of eukaryotic nuclear DNA replication.

General Description

A cell-permeable tetracyclic diterpene antibiotic. Cell synchronization agent. Blocks the cell cycle at the early S-phase. Specific inhibitor of DNA polymerase α and δ in eukaryotic cells and in some viruses of animal origin. Potentiates apoptosis induced by arabinosyl nucleosides in leukemia cell lines. Also induces apoptosis in HeLaS3 cells, but inhibits vincristine-induced apoptosis in the p53-negative human prostate cancer cell line PC-3.

Biochem/physiol Actions

Cell permeable: yes

storage

+4°C

References

1) Syvaoja et al. (1990), DNA polymerases alpha, delta, and epsilon: three distinct enzymes from HeLa cells; Proc. Natl. Acad. Sci. USA, 87 6664 2) Urbani et al. (1995), Dissociation of nuclear and cytoplasmic cell cycle progression by drugs employed in cell synchronization; Exp. Cell Res., 219 159 3) Kuwakado et al. (1993), Aphidicolin potentiates apoptosis induced by arabinosyl nucleosides in human myeloid leukemia cell lines; Biochem. Pharmacol., 46 1909 4) Yin and Schimke (1996), Inhibition of apoptosis by overexpressing Bcl-2 enhances gene amplification by a mechanism independent of aphidicolin pretreatment; Proc. Natl. Acad. Sci. USA, 93 3394

APHIDICOLIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 132)Suppliers
Supplier Tel Email Country ProdList Advantage
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387 1057@dideu.com China 3586 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9358 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
Alfa Chemistry
+1-5166625404 Info@alfa-chemistry.com United States 21317 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58

View Lastest Price from APHIDICOLIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
APHIDICOLIN USP/EP/BP pictures 2021-06-25 APHIDICOLIN USP/EP/BP
38966-21-1
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
(+)-Aphidicolin, Nigrospora oryzae  pictures 2020-05-10 (+)-Aphidicolin, Nigrospora oryzae
38966-21-1
US $1.00 / KG 1KG 99% 20T Shaanxi Dideu Medichem Co. Ltd
APHIDICOLIN pictures 2019-12-26 APHIDICOLIN
38966-21-1
US $1.00 / g 1g ≥98% g/kg/Ton Career Henan Chemical Co
  • APHIDICOLIN pictures
  • APHIDICOLIN
    38966-21-1
  • US $1.00 / g
  • ≥98%
  • Career Henan Chemical Co
(3-ALPHA,4-ALPHA,5-ALPHA,17-ALPHA)-3,17-DIHYDROXY-4-METHYL-9,15-CYCLO-C,18-DINOR-14,15-SECOANDROSTANE-4,17-DIMETHANOL (+)-APHIDICOLIN APHIDICOLIN (+)-APHIDICOLIN, NIGROSPORA ORYZAE ,11a-beta,11b-beta))- 9-dimethanol,tetradecahydro-3,9-11a-methano-11ah-cyclohepta(a)naphthalene-4 dihydroxy-4,11b-dimethyl-,(3r-(3-alpha,4-alpha,4a-alpha,6a-beta,8-beta,9-beta ici69653 nsc-234714 APHIDICOLIN FROM CEPHALOSPORIUM APHIDICO LA APHIDICOLIN FROM NIGROSPORA SPHAERICA 8,11a-Methano-11aH-cycloheptaanaphthalene-4,9-dimethanol, tetradecahydro-3,9-dihydroxy-4,11b-dimethyl-, (3R,4R,4aR,6aS,8R,9R,11aS,11bS)- Aphidicolin, froM Nigrospora oryzae 8,11|á-Methano-11aH-cyclohepta[a]naphthalene-4,9-dimethanol,tetradecahydro-3,9-dihydroxy-4,11b-dimethyl-, (3R,4R,4aR,6aS,8R,9R,11aS,11bS)- Aphidicolin NSC 234714 ICI 69653 Aphidicolin, Ready Made Solution Aphidicolin - CAS 38966-21-1 - Calbiochem InSolution Aphidicolin - CAS 38966-21-1 - Calbiochem APHIDICOLIN USP/EP/BP Aphidicolin, 98%, from Nigrospora oryzae (3R,4R,4aR,6aS,8R,9R,11aS,11bS)-Tetradecahydro-3,9-dihydroxy-4,11b-dimethyl-8,11a-methano-11aH-cyclohepta[a]naphthalene-4,9-dimethanol APC 8,11|á-Methano-11aH-cyclohepta[a]naphthalene-4,9-dimethanol,tetradecahydro-3,9-dihydroxy-4,11b-dimethyl-, (3R,4R,4aR,6aS,8R,9R,11aS,11bS)- 38966-21-1 BioChemical Antibiotics A to Z Antibiotics A-F Antibiotics antibiotic Di-Terpenoids