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Vinblastine sulfate

CAS No.
143-67-9
Chemical Name:
Vinblastine sulfate
Synonyms
VLB;exal;velban;VINCALEUKOBLASTINE;VINBLASTINE SULFATE SALT;velbe;Velsar;29060le;nsc49842;Periblastine
CBNumber:
CB7407655
Molecular Formula:
C46H60N4O13S
Molecular Weight:
909.05
MDL Number:
MFCD00082457
MOL File:
143-67-9.mol
Last updated:2023-09-07 18:57:57

Vinblastine sulfate Properties

Melting point 267 °C (dec.)(lit.)
alpha -21.7 º (c=2, CH3OH 21 ºC)
storage temp. 2-8°C
solubility H2O: 10 mg/mL
form powder
color white
PH 3.5~5.0 (1g/l, 25℃)
Water Solubility >=1 g/100 mL at 24.5 ºC
Merck 13,10044
BRN 3659812
InChIKey KDQAABAKXDWYSZ-PNYVAJAMSA-N
CAS DataBase Reference 143-67-9(CAS DataBase Reference)
EWG's Food Scores 1
NCI Dictionary of Cancer Terms Velban; vinblastine sulfate
FDA UNII N00W22YO2B
NCI Drug Dictionary vinblastine sulfate
Proposition 65 List Vinblastine Sulfate
IARC 3 (Vol. 26, Sup 7) 1987
EPA Substance Registry System Vinblastine sulfate (143-67-9)

Pharmacokinetic data

Protein binding 99%
Excreted unchanged in urine 14%
Volume of distribution 13-40(L/kg)
Biological half-life 25 / -

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H341-H361fd
Precautionary statements  P202-P264-P270-P280-P301+P312-P308+P313
Hazard Codes  Xn,T
Risk Statements  22-37/38-41-61-36/37/38-63-23/24/25
Safety Statements  26-36/39-53-45-37/39-36/37/39
RIDADR  1544
WGK Germany  3
RTECS  YY8400000
8-10
HazardClass  6.1(a)
PackingGroup  II
HS Code  29399990
Toxicity LD50 i.v. in mice: 9.5 mg/kg (Lu, Meistrich)
NFPA 704
0
3 0

Vinblastine sulfate price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR2698 Vinblastine Sulfate Pharmaceutical Secondary Standard; Certified Reference Material, certified reference material, pharmaceutical secondary standard, pkg of 100?mg 143-67-9 100MG $365 2024-03-01 Buy
Sigma-Aldrich 1713004 Vinblastine sulfate United States Pharmacopeia (USP) Reference Standard 143-67-9 50mg $993 2024-03-01 Buy
Alfa Aesar J63598 Vinblastine sulfate 98% 143-67-9 10mg $114 2023-06-20 Buy
Alfa Aesar J63598 Vinblastine sulfate 98% 143-67-9 50mg $417 2023-06-20 Buy
Cayman Chemical 11762 Vinblastine (sulfate) ≥95% 143-67-9 5mg $57 2024-03-01 Buy
Product number Packaging Price Buy
PHR2698 100MG $365 Buy
1713004 50mg $993 Buy
J63598 10mg $114 Buy
J63598 50mg $417 Buy
11762 5mg $57 Buy

Vinblastine sulfate Chemical Properties,Uses,Production

Description

Vinblastine sulfate is the salt of an alkaloid extracted from Vinca rosea Linn., a common flowering herb known as the periwinkle (more properly known as Catharanthus roseus G. Don). Previously, the generic name was vincaleukoblastine, abbreviated VLB. It is a stathmokinetic oncolytic agent. When treated in vitro with this preparation, growing cells are arrested in metaphase. Chemical and physical evidence indicate that vinblastine sulfate is a dimeric alkaloid containing both indole and dihydroindole moieties.

Chemical Properties

Vinblastine sulfate is a white to off-white crystalline powder that is freely soluble in water, soluble in methane, and slightly soluble in ethanol. Its empiric formula is C46H58N4O9.H2SO4 , and it has a molecular weight of 909.07.

Originator

Velban ,Lilly ,US ,1961

Uses

Vinblastin sulfate USP (Velban) is used to treat Hodgkin’s disease; lymphosarcoma; reticulum cell sarcoma; neuroblastoma; choriocarcinoma; carcinoma of breast, lung, oral cavity, testis, bladder; acute and chronic leukemia; histiocytosis; mycosis fungoides.

Uses

Anticancer agent; microtubule disrupter; Induces apoptosis.Vinblastine sulfate is therapeutically used as an antineoplastic. It is also used in the treatment of Hodgkin disease, choriocarcinoma, acute and chronic leukemias.

Definition

ChEBI: Vincaleukoblastine sulfate is an alkaloid sulfate salt. It is functionally related to a vincaleukoblastine.

brand name

Velban (Lilly).

Therapeutic Function

Cancer chemotherapy

General Description

Vinblastine Sulfate is the sulfate salt of vinblastine, a natural alkaloid isolated from the plant Catharanthus roseus (Madagascar periwinkle) with antineoplastic properties. Vinblastine disrupts microtubule formation and function during mitosis and interferes with glutamic acid metabolism. (NCI04)

Air & Water Reactions

Water soluble..Rapidly hydrolyzes.

Reactivity Profile

Vinblastine sulfate is sensitive to light, hydrolysis, oxidation, and heat. Vinblastine sulfate is very hygroscopic. .

Health Hazard

SYMPTOMS: Symptoms of exposure to Vinblastine sulfate include temporary mental depression, paresthesias, loss of deep-tendon reflexes, headache, convulsions, psychoses; dysfunction of the autonomic nervous system, with marked constipation, paralytic ileus, urinary retention, bilateral pain and tenderness of the parotid glands associated with dryness of the mouth, sinus tachycardia; nausea, vomiting, anorexia, diarrhea; loss of hair, vesicular mucositis of the mouth, and dermatitis.

Biological Activity

Anticancer agent; microtubule disrupter. Induces apoptosis in cultured hepatocytes and human lymphoma cells.

Biochem/physiol Actions

Primary TargetInteraction of tubulin with microtubule-associated proteins, specifically Tau and MAP2

Clinical Use

Vinblastine sulfate is available as a powder in 10-mg vials and as a solution in 10- and 25-mL vials for IV administrationin the treatment of various cancers including Hodgkin’sdisease, lymphocytic lymphoma, histiocytic lymphoma, advancedmycosis fungoides, advanced testicular carcinoma,and Kaposi sarcoma. It has also been used in treating choriocarcinomaand breast cancer when other therapies havefailed.

Side effects

The major toxic effect of vinblastine is a dose-related bone marrow depression. This is more frequent and severe than with the close structural analog, vincristine. Dose-related leukopenia occurs with a nadir of 4 to 10 days and with recovery occurring over another 7 to 14 days. Because of the relatively predictable nadir, it may be possible to administer vinblastine cautiously as often as every 7 to 10 days. Thrombocytopenia typically occurs; however, with standard dosing regimens, serious platelet depressions are infrequent. Erythrocytes are usually only slightly depressed.

Safety Profile

Poison by ingestion, intraperitoneal, and intravenous routes. An experimental teratogen. Human systemic effects by intravenous route: blood leukopenia and hair changes. Experimental reproductive effects. Questionable carcinogen. Human mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also VINCALEUKOBLASTINE and SULFATES.

Veterinary Drugs and Treatments

Vinblastine may be employed in the treatment of lymphomas, carcinomas, mastocytomas, and splenic tumors in small animals. It is more effective than vincristine in the treatment of canine mast cell tumors.

Drug interactions

Potentially hazardous interactions with other drugs
Aldesleukin: avoid concomitant use.
Antibacterials: toxicity increased by erythromycin - avoid; possible increased risk of ventricular arrhythmias with delamanid.
Antiepileptics: phenytoin levels may be reduced.
Antifungals: possible increased risk of toxicity with itraconazole; metabolism possibly inhibited by posaconazole (increased risk of neurotoxicity).
Antimalarials: avoid with piperaquine with artenimol.
Antipsychotics: avoid with clozapine (increased risk of agranulocytosis).

Metabolism

Vinblastine is extensively metabolised mainly in the liver by the CYP3A group of isoenzymes to desacetylvinblastine, which is more active than the parent compound. 33
% of the drug is slowly excreted in the urine and 21
% in the faeces within 72 hours.

storage

Store at -20°C

Purification Methods

Crystallise the sulfate from MeOH or EtOH and dry it in vacuo over conc H2SO4. The free base crystallises from EtOH or MeOH m 211-216o (+ 2MeOH .1 H2O) and forms a stable etherate from Et2O with m 201-211o, and [] D +42o (CHCl3), and UV max at 214 and 259nm (log  4.73 and 4.21). The dihydrochloride has m 244-246o(dec)(MeOH). It is a monoamine oxidase B inhibitor and induces microtubule aggregation. It is an antineoplastic drug for Hodgkin’s lymphoma. [Neuss et al. J Am Chem Soc 81 4754 1959, Jong-KeunSon et al. J Med Chem 33 1845 1990, Warfield & Bouck Science 186 1219 1974, Beilstein 26 III/IV 3167.]

Mode of action

Vinblastine binds to tubulin and inhibits microtubule assembly. This inhibition prevents mitotic spindle formation and results in an accumulation of cells in metaphase.
Vinblastine is considered cell cycle phase specic for mitosis; however, the cytotoxic effect probably occurs in S phase and is expressed only in M phase. At high doses, direct effects may be expressed in S and G1 phases. Vinblastine is assumed to have stathmokinetic (cell cycle arrest) effects similar to vincristine.

124096-76-0
143-67-9
Synthesis of Vinblastine sulfate from Ethanamine, N-[(3,5-dichlorophenyl)methylene]-2,2-diethoxy-

Vinblastine sulfate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 467)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907 qinhe02@xaltbio.com China 1000 58
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
Nanjing Finetech Chemical Co., Ltd.
025-85710122 17714198479 sales@fine-chemtech.com CHINA 885 55
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
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028-87075086 13350802083 scglp@glp-china.com CHINA 1824 58
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+86 18953170293 sales@sdzschem.com China 2931 58
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+86-15008981366 15008981366@163.com CHINA 9 58
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10248 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897 sales@biopurify.com China 3424 58

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View Lastest Price from Vinblastine sulfate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Vinblastine Sulfate pictures 2024-04-15 Vinblastine Sulfate
143-67-9
US $1.00-100.00 / mg 100mg 0.99 5ton/month ANHUI SHENGZHIKAI BIOTECHNOLOGY CO.,LTD
Vinblastine sulfate pictures 2024-04-12 Vinblastine sulfate
143-67-9
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
Vinblastine sulfate pictures 2024-03-16 Vinblastine sulfate
143-67-9
US $0.00 / KG 100g 98%+ 100kg WUHAN CIRCLE POWDER TECHNOLOGY CO.,LTD

Vinblastine sulfate Spectrum

29060le nsc49842 rozevinsulfate velbe vincaleukoblastine,sulfate(1:1)(salt) Vinblastine, sulphate salt VLB, Vincaleukoblastine sulphate salt Vinblastine Sulphate USP Vineblastine sulfate salt Vinblastine sulfate sa VINBLASTINE, VLB Vinblastine Sulfate, Vincaleukoblastine, VLB Vincaleukoblastine sulfate salt, VLB 3aR-(3aalpha,4beta,5beta,5abeta,9(3R*,5S*,7R*,9S*),10bR*,13aalpha)-methyl 4-(acetyloxy)-3a-ethyl-9-(5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-9-(methoxycarbonyl)-2H-3,7-methanoazacycloundecino[5,4-b]indol-9-yl)-3a,4,5,5a,6,11,12,13a-octahydro-5-hydroxy Vinblastine sulfate,96-102% % Vinblastine sulfate salt,VLB, Vincaleukoblastine sulfate salt Vinblastine Sulfate (50 mg) Vinblastine-d3 Vinblastine Sulfate(Vincaleukoblastine) Periblastine VINBLASTINE SULPHATE VINCALEUKOBLASTINE SULFATE VINCALEUKOBLASTINE SULFATE SALT VINBLASTINE SULFATE Vinblastin Sulfate VINBLASTINE SULFATE, CRYSTALLIZED VINBLASTINE SULFATE CRYST VINBLASTINE SULFATE 98+% BP USP Vinblastine Sulfate USP XXI Vinblastine sulfate, 96.0-102.0% 29060-LE, Exal, Velban, Velbe, VINBLASTINESULFATE,USP Velsar Vincaleucoblastine sulfate Vincaleukoblastine, sulfate (1:1) (salt) (8CI, 9CI) VLB monosulfate VINCALEUKOBLASTINE,SULPHATE VINBLASTINSULPHATE Vinblastine sulfate, Antibiotic for Culture Media Use Only Vinblastine Sulfate, >=98% Vinblastine Sulfate - CAS 143-67-9 - Calbiochem Vinblastine Sulfate (Vincristine EP Impurity H Sulfate) Vinorelbine Impurity 3 Vinblastine sulfate 143-67-9 Vinblastine Sufate Vinblastine sulfate CRS Vinblastine Sulfate RS Vinblastine sulfate USP/EP/BP Vinblastine sulfate (NSC49842) Vinblastine Sulfate (1713004) 3S)-3-Phenylisoserine hydrochloride exal velban VINBLASTINE SULFATE SALT VINCALEUKOBLASTINE VLB vincaleukoblastine,sulfate(1:1) Vincristine EP Impurity H(vinblastine) Sulfate