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Auristatin F-d8

Auristatin F-d8 is deuterium labeled Auristatin F. Auristatin F is a potent cytotoxin in antibo-conjugated agents and an analogue of MMAF. Auristatin F is a potent microtubule inhibitor and vascular damaging agent (VDA). Auristatin F inhibits cell division by preventing tubulin aggregation.Auristatin F can be used in antibody-drug conjugates (ADC).

Product Specifications

UNSPSC

12352005

Hazard Statement

H300+H330, H340, H360, H370, H372, H412

Target

ADC Payload; Isotope-Labeled Compounds; Microtubule/Tubulin

Type

Isotope-Labeled Compounds

Related Pathways

Antibody-drug Conjugate/ADC Related; Cell Cycle/DNA Damage; Cytoskeleton; Others

Applications

Cancer-programmed cell death

Field of Research

Cancer

Purity

99.82

Solubility

10 mM in DMSO

Smiles

CC([C@@H](C(N[C@@]([2H])(C(C([2H])([2H])[2H])(C([2H])([2H])[2H])[2H])C(N(C)[C@H]([C@H](OC)CC(N1CCC[C@]1([C@@H]([C@H](C(N[C@@H](CC2=CC=CC=C2)C(O)=O)=O)C)OC)[H])=O)[C@H](CC)C)=O)=O)N(C)C)C

Molecular Formula

C40H59D8N5O8

Molecular Weight

754.04

Precautions

H300+H330, H340, H360, H370, H372, H412

References & Citations

[1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53 (2) :211-216.|[2]Park MH, et, al. Pharmacokinetic and Metabolism Studies of Monomethyl Auristatin F via Liquid Chromatography-Quadrupole-Time-of-Flight Mass Spectrometry. Molecules. 2019 Jul 29;24 (15) :2754.|[3]Roy S, et al. SMI-Ribosome inactivating protein conjugates selectively inhibit tumor cell growth. Chem Commun (Camb) . 2017 Apr 11;53 (30) :4234-4237.

Shipping Conditions

Blue Ice

Storage Conditions

-20°C, 3 years (Powder)

Scientific Category

Isotope-Labeled Compounds

Clinical Information

No Development Reported

Frequently Asked Questions

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