Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Vinblastine inhibits microtubule formation and supresses nAChR activity with IC50 of 8.9 μM.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Alkaloids and derivatives |
| Classe | Vinca alkaloids |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Vinca alkaloids |
| Alternative Parents | Carbazoles 3-alkylindoles Tricarboxylic acids and derivatives Anisoles Dialkylarylamines Alkyl aryl ethers Aralkylamines Piperidines N-alkylpyrrolidines Tertiary alcohols Pyrroles Methyl esters Heteroaromatic compounds Trialkylamines Cyclic alcohols and derivatives 1,2-aminoalcohols Amino acids and derivatives Azacyclic compounds Carbonyl compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Vinca alkaloid skeleton - Carbazole - 3-alkylindole - Tricarboxylic acid or derivatives - Indole or derivatives - Indole - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Anisole - Aralkylamine - Alkyl aryl ether - Piperidine - Benzenoid - N-alkylpyrrolidine - Methyl ester - Tertiary alcohol - Pyrrole - Heteroaromatic compound - Pyrrolidine - Cyclic alcohol - 1,2-aminoalcohol - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Azacycle - Ether - Carboxylic acid derivative - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - Aromatic heteropolycyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as vinca alkaloids. These are alkaloids with a dimeric chemical structure composed of an indole nucleus (catharanthine), and a dihydroindole nucleus (vindoline), joined together. |
| External Descriptors | Not available |
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| Solubilidade | 25°C: DMSO 67 mg/mL; Water <1 mg/mL; Ethanol 7 mg/mL |
|---|---|
| Sensibilidade | Moisture and light sensitive |
| Peso molecular | 811.000 g/mol |
| XLogP3 | 3.700 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 10 |
| Exact Mass | 810.42 Da |
| Monoisotopic Mass | 810.42 Da |
| Topological Polar Surface Area | 154.000 Ų |
| Heavy Atom Count | 59 |
| Formal Charge | 0 |
| Complexity | 1700.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 9 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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