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Teniposide

Product Name
Teniposide
CAS No.
29767-20-2
Chemical Name
Teniposide
Synonyms
etp;vehem;vm-26;Vumon;Eniposide;nsc122819;Teniposid;Tenoposide;nsc-122819;TENIPOSIDE
CBNumber
CB0455475
Molecular Formula
C32H32O13S
Formula Weight
656.65
MOL File
29767-20-2.mol
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Teniposide Property

Melting point:
244-247°C
alpha 
D20 -107° (9:1 chloroform/methanol)
Boiling point:
650.86°C (rough estimate)
Density 
1.2568 (rough estimate)
refractive index 
1.5530 (estimate)
storage temp. 
-20°C
solubility 
DMSO: soluble10mg/mL, clear
pka
10.13(at 25℃)
form 
powder
color 
white to beige
optical activity
[α]/D -100 to -115°, c = 1 in chloroform/methanol (9:1)
λmax
283nm(MeOH)(lit.)
Merck 
14,9145
Stability:
Hygroscopic
CAS DataBase Reference
29767-20-2(CAS DataBase Reference)
IARC
2A (Vol. 76) 2000
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Safety

Hazard Codes 
Xi,T
Risk Statements 
36/37/38-45
Safety Statements 
26-36-45-53
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
RTECS 
KC0180000
HS Code 
29349990
Hazardous Substances Data
29767-20-2(Hazardous Substances Data)
Toxicity
LD50 intraperitoneal in mouse: 29570ug/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H341Suspected of causing genetic defects

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P202Do not handle until all safety precautions have been read and understood.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0609
Product name
Teniposide
Purity
≥97% (HPLC)
Packaging
10mg
Price
$76.2
Updated
2025/07/31
Sigma-Aldrich
Product number
1643736
Product name
Teniposide
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$429
Updated
2022/05/15
TCI Chemical
Product number
T3109
Product name
Teniposide
Purity
>98.0%(HPLC)
Packaging
20mg
Price
$101
Updated
2025/07/31
TCI Chemical
Product number
T3109
Product name
Teniposide
Purity
>98.0%(HPLC)
Packaging
100mg
Price
$323
Updated
2025/07/31
Cayman Chemical
Product number
14425
Product name
Teniposide
Purity
≥98%
Packaging
10mg
Price
$32
Updated
2024/03/01
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Teniposide Chemical Properties,Usage,Production

Chemical Properties

White Solid

Originator

Vehem,Sandoz,France,1976

Uses

Teniposide is a podophyllotoxin derivative that causes dose-dependent single- and double-stranded breaks in DNA by inhibiting topoisomerase II. Its cytostatic effects are related to its ability to stabilize the DNA-topoisomerase II complex during DNA replication, inducing DNA damage and cellular apoptosis. Teniposide has been widely used in the treatment of various cancers including, small cell lung cancer, malignant lymphoma, breast cancer, oral squamous cell carcinoma, and acute lymphoblastic leukemia.

Uses

A labelled semi-synthetic derivative of Podophyllotoxin. Antineoplastic.

Uses

A semi-synthetic derivative of Podophyllotoxin. Antineoplastic.

Indications

Teniposide (VM-26, Vumon) is closely related to etoposide in structure, mechanisms of action and resistance, and adverse effects. It is more lipophilic and approximately threefold more potent than etoposide. Its major uses have been in pediatric cancers, particularly in acute lymphoblastic leukemias.

Definition

ChEBI: A furonaphthodioxole that is a synthetic derivative of podophyllotoxin with anti-tumour activity; causes single- and double-stranded breaks in DNA and DNA-protein cross-links and prevents repair by topoisomerase II binding.

Manufacturing Process

10 ml of pure thiophene-2-aldehyde and 0.25 g of anhydrous zinc chloride are American Home Products Corporation; British Patent 1,022,642; March 16, 1966
American Home Products Corporation; British Patent 1,022,645; March 16, 1966
Bell, S.C.; British Patent 1,057,492; February 1, 1967; assigned to American Home Products Corporation

brand name

Vumon (Bristol-Myers Squibb).

Therapeutic Function

Antineoplastic

General Description

Teniposide is available in 50-mg ampules with Cremophor ELfor IV administration in the treatment of acute lymphoblasticleukemia (ALL). The agent is more potent as an inhibitor oftopoisomerase II. The pharmacokinetics of teniposide issimilar to that of etoposide; however, the more lipophilic teniposideis more highly protein bound (99%) and less isexcreted unchanged in the urine (10%–20%). There is alsogreater overall metabolism of teniposide; however, CYP3A4-mediated conversion to the active catechol is slower comparedwith etoposide. Elimination occurs primarily in the urine witha terminal elimination half-life of 5 hours.

Biochem/physiol Actions

Teniposide (VM-26) is a Topoisomerase II inhibitor with antitumor activity. Teniposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA, inducing breaks in double stranded DNA and preventing repair.

Clinical Use

Teniposide is used in combination with other agents for the treatment of refractory childhood acute lymphoblastic leukemia.

Safety Profile

Poison by intraperitoneal and subcutaneous routes. An experimental teratogen. Human systemic effects by ingestion and intravenous route: anorexia, nausea or vomiting, leukopenia, agranulocytosis and aplastic anemia of the blood, bone marrow changes, and hair changes. Experimental reproductive effects. Human mutation data reported. When heated to decomposition it emits very toxic fumes of SOx.

Synthesis

Teniposide, [5R-(5|á,5a|?,8a|á,9|?)]-9-[4,6-O-(2-thienylmethylene)-|?-D-glucopyranosyl)oxy]- 5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)furo[3,4: 6,7]-naphtho[2,3-d]-1,3-dioxol-6(5aH)-one (30.4.9), is basically synthesized by an analogous scheme from 4-benzyloxy-4-desmethylepipodophyllotoxin (30.4.6), which is esterified by 2,3,4,6- tetra-O-acetyl-|?-D-glucose in the presence of boron trifluoride etherate, giving a glycoside 30.4.7. The acetyl and benzyloxycarbonyl protecting groups in this molecule are removed by succesive use of zinc acetate and sodium methoxide, and then by subsequent hydrogen reduction, which forms the diol 30.4.8. The resulting diol is then transformed into the corresponding acetal 2-formylthiophene, which is the desired teniposide (30.4.9) .

storage

Store at -20°C

Teniposide Preparation Products And Raw materials

Raw materials

Preparation Products

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Teniposide Suppliers

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View Lastest Price from Teniposide manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Teniposide 29767-20-2
Price
US $0.00/Kg/Bag
Min. Order
10g
Purity
98%min
Supply Ability
10kg
Release date
2021-09-23
Zhuozhou Wenxi import and Export Co., Ltd
Product
Teniposide 29767-20-2
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-08-11
Zhuozhou Wenxi import and Export Co., Ltd
Product
Teniposide 29767-20-2
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10

29767-20-2, TeniposideRelated Search:


  • (5R,5aα)-5α,8,8aβ,9β-Tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[4-O,6-O-[(R)-2-thienylmethylene]-β-D-glucopyranosyl]oxy]furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one
  • 4'-Demethylepipodophyllotoxin-9-(4,6-O-2-thenylidene β-D-glucopyranoside)
  • 4’-Demethylepipodophyllotoxin9-(4,6-o-2-thenylidene-
  • 4'-Demethylepipodophyllotoxin thenylidene glucoside
  • Epipodophyllotoxin, 4'-demethyl-, 9-(4,6-o-2-thienylidene-.beta.-D-glucopyranoside)
  • Furo[3',4':6,7]naphtho[2,3-D]-1,3-dioxol-6(5ah)-one, 5,8,8A,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[4,6-o-(2-thienylmethylene)-.beta.-D-glucopyranosyl]oxy]-, [5R-(5.alpha.,5A.beta.,8A.alpha.,9.beta.)]-
  • (10R,11R,15R,16S)-16-{[(2R,4aR,6R,7R,8R,8aS)-7,8-dihydroxy-2-(thiophen-2-yl)-hexahydro-2H-pyrano[3,2-d][1,3]dioxin-6-yl]oxy}-10-(4-hydroxy-3,5-diMethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1,3(7),8-trien-12-one
  • Teniposide(VuMon)
  • (10R,11R,15R,16R)-16-{[(4aR,7R,8R,8aS)-7,8-dihydroxy-2-(thiophen-2-yl)-hexahydro-2H-pyrano[3,2-d][1,3]dioxin-6-yl]oxy}-10-(4-hydroxy-3,5-diMethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1(9),2,7-trien-12-one
  • (5R,5aR,8aR,9S)-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[4,6-O-[(R)-2-thienylmethylene]-β-D-glucopyranosyl]oxy]-furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one
  • 4′-Dimethyl-9-(4,6-O-2-thenyid)-epipodophyllotoxin
  • Tenoposide
  • Eniposide
  • 4’-demethylepipodophyllotoxin9-(4,6-o-2-thenylidene-beta-d-glucopyranoside)
  • 4’-demethyl-epipodophyllotoxin-beta-d-thenylidene-glucosid
  • 4’-demethyl-epipodophyllotoxin-beta-d-thenylidene-glucoside
  • 4’-demethylepipodophyllotoxin-beta-d-thenylidineglucoside
  • 5abeta,8aalpha,9beta(r*)]]-5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-[5r-[5alph
  • dimethoxyphenyl)-9]]4-6-o-(2-thienylmethylene)-beta-d-glucopyranosyl]oxy]furo[
  • epipodophyllotoxin,4’-demethyl-,9-(4,6-o-2-thenylidene-beta-d-glucopyranoside
  • etp
  • eniposide, Vumon, VM-26
  • 3’,4’:6,7]naphtho[2,3-d]-1,3-dioxol-6(5ah)-one
  • 4’-demethyl1-o-(4,6-o,o-(2-thenylidene)-beta-d-glucopyranosyl)epipodophyllot
  • 4’-demethyl1-o-(4,6-o,o-(2-thenylidene)-beta-d-glucopyranosyl)epipodophylloto
  • 4’-demethylepipodophyllotoxin9-(4,6-o-2-thenylidene-bata-d-glucopyranoside.
  • nsc122819
  • nsc-122819
  • TENIPOSIDE
  • vehem
  • vm-26
  • Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one, 5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[4,6-O-[(R)-2-thienylmethylene]-b-D-glucopyranosyl]oxy]-, (5R,5aR,8aR,9S)-
  • [5R-[5alpha,5abeta,8aalpha,9beta(R*)]]-5,8,8a,9-Tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[4,6-O-(2-thienylmethylene)-beta-D-glucopyranosyl]oxy]-furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one
  • 4'-Demethyl 1-O-(4,6-O,O-(2-thenylidene)-beta-D-glucopyranosyl)epipodophyllotoxin
  • Furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5aH)-one, 5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-((4,6-O-(2-thienylmethylene)-beta-D-glucopyranosyl)-oxy)-, (5R-(5alpha,5abeta,8aalpha,9beta(R*)))
  • Pipodophyllotoxin VM 26
  • Vumon
  • 4'-Dimethylepipodophyllotoxin-9-(4,6-O-2-thenylidene)-b-D-glucopyranoside
  • Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one, 5,8,8a,9-tetrahydro-5-(4-hydroxy-3,5-dimethoxyphenyl)-9-[[4,6-O-[(R)-2-thienylmethylene]-β-D-glucopyranosyl]oxy]-, (5R,5aR,8aR,9S)-
  • Teniposide USP/EP/BP
  • Teniposide Impurity 2
  • Teniposide (1643736)
  • Methylguanidoacetic acid monohydrate
  • (5R,5aR,8aR,9S)-9-(((2R,4aR,6R,7R,8R,8aS)-7,8-Dihydroxy-2-(thiophen-2-yl)hexahydropyrano[3,2-d][1,3]dioxin-6-yl)oxy)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5,5a,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8H)-one
  • Teniposid
  • Teniposide (200 mg) (PLANNED TO BE DISCONTINUED)
  • 4'-Dimethylepipodophyllotoxin-(4,6-O-2-thenylidene)-beta-D-glucopyranoside
  • Teniposide, 10 mM in DMSO
  • Teniposide - Bio-X ?
  • (5r,5ar,8ar,9s)-9-(((2r,4ar,6r,7r,8r,8as)-7,8-dihydroxy-2-(thiophen-2-yl)hexahydropyrano[3,2-d][1,3]dioxin-6-yl)oxy)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5,8,8a,9-tetrahydrofuro[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(5ah)-one
  • 29767-20-2
  • 29707-20-2
  • 29767-20-7
  • C32H32O13S
  • C32H29D3O13S
  • Carbohydrates & Derivatives
  • Chiral Reagents
  • Heterocycles