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Filtered Search Results
NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 696731772](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000161175.jpg-250.jpg)
eMolecules 159610-89-6 | Fmoc-Lys(N3)-OH | Ambeed | MFCD13182319 | 394.431 | C21H22N4O4 | 95.000 | OC(=O)[C@H](CCCCN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 696731772
Fmoc-Lys(N3)-OH | Ambeed | 159610-89-6 | MFCD13182319 | 394.431 | C21H22N4O4 | 95.000 | OC(=O)[C@H](CCCCN=[N+]=[N-])NC(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 696731772
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Medchemexpress LLC Maleimidocaproyl-monomethylauristatin E | 863971-24-8 | MFCD28167757 | 99.9% | 911.18 | C49H78N6O10 | 25 MG
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Mc-MMAE (maleimidocaproyl-monomethylauristatin E) is a maleimidocaproyl-protected monomethyl auristatin E used as an agent-linker conjugate in antibody-drug conjugate research. It functions as a potent tubulin inhibitor and is supplied as a solid for conjugation and synthesis of ADCs.
- Protective maleimidocaproyl linker conjugated to monomethyl auristatin E.
- Potent tubulin inhibitor for ADC payload development.
- High purity suitable for research applications.
- Solid form, white to light yellow, unstable in solution; prepare fresh.
- Molecular formula C49H78N6O10 and molecular weight 911.18.
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Medchemexpress LLC HY-100567 10mg , MAL-di-EG-Val-Cit-PAB-MMAE CAS: Purity:98%
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Medchemexpress, HY-100567 10mg MAL-di-EG-Val-Cit-PAB-MMAE CAS: Formula:C72H112N12O18 Purity:98% MAL-di-EG-Val-Cit-PAB-MMAE consists the ADCs linker (MAL-di-EG-Val-Cit-PAB) and potent tubulin inhibitor (MMAE), MAL-di-EG-Val-Cit-PAB-MMAE is an antibody drug conjugate. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Boc-Val-Ala-PAB | 1884577-99-4 | 99.9% | 393.48 | 500 MG
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Boc-Val-Ala-PAB is a cathepsin cleavable ADC linker utilized in the creation of antibody-drug conjugates (ADCs). ADCs consist of an antibody to which an ADC cytotoxin is attached via an ADC linker. This product is for research use only.
- Cathepsin cleavable linker
- Used for making antibody-drug conjugates
- Supports the attachment of cytotoxins to antibodies
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Bachem Z-Val-OH
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Z-Val-OH, 1149-26-4, C13H17NO4, Mr 251.28, 25g.
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Medchemexpress LLC HY-114202 10mg Medchemexpress, delta-Valerobetaine CAS:6778-33-2 Purity:>98%
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Medchemexpress, HY-114202 10mg delta-Valerobetaine CAS:6778-33-2 delta-Valerobetaine is a precursor of trimethylamine N-oxide (TMAO). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC L-isoleucyl-L-valine (Ile-Val) | 41017-96-3 | MFCD00038332 | 95.0% | 230.30 g/mol | C11H22N2O3 | 5 MG
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L-isoleucyl-L-valine (Ile-Val) is a dipeptide composed of L-isoleucine and L-valine that induces the bovine trypsinogen-to-trypsin transition. It is supplied as a solid research reagent (CAS 41017-96-3) with typical purity of 95.0% and a molecular weight of 230.30 g/mol.
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C(=O)N[C@@H](C)C(=O)Nc1ccc(CO)cc1 | 1g | 837438949](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000471294.jpg-250.jpg)
eMolecules 1343476-44-7 | Val-Ala-PAB | ChemScene293.367 | C15H23N3O3 | 97.000 | CC(C)[C@H](N)C(=O)N[C@@H](C)C(=O)Nc1ccc(CO)cc1 | 1g | 837438949
Val-Ala-PAB | ChemScene | 1343476-44-7293.367 | C15H23N3O3 | 97.000 | CC(C)[C@H](N)C(=O)N[C@@H](C)C(=O)Nc1ccc(CO)cc1 | 1g | 837438949
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Medchemexpress LLC Mc-val-cit-pab-cl | 1639351-92-0 | MFCD32201033 | 95.0% | 591.10 | C28H39ClN6O6 | 5 MG
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Mc-Val-Cit-PAB-Cl is a cleavable antibody-drug conjugate (ADC) linker that combines a valine-citrulline dipeptide with a para-aminobenzyl (PAB) self-immolative spacer to enable protease-triggered release of cytotoxic payloads such as MMAE. Supplied as a solid reagent with defined purity, it is intended for ADC linker synthesis and conjugation workflows; follow recommended low-temperature, inert storage for stability.
- Cleavable val-cit dipeptide linked to a PAB self-immolative spacer.
- Designed for protease-triggered release of payloads such as MMAE.
- Provided as a solid reagent suitable for conjugation reactions.
- High purity for research-grade synthesis and analytical consistency.
- Stable when stored under inert atmosphere at recommended low temperatures.
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STA PHARMACEUTICAL US LLC Fmoc-D-IsoValine | 10 g | CAS 1231709-22-0 | MDL MFCD12031689
Fmoc-D-IsoValine is a Amino Acid reagent (Subcategory: Alkane AA) sold by WuXi TIDES. Offered in 10 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 1231709-22-0
- MDL: MFCD12031689
- InChIKey: DZSLHAJXIQCMLR-HXUWFJFHSA-N
- Molecular Weight: 339.391
- Molecular Formula: C20H21NO4
- Purity: ≥95%
- Container Type: 60 mL HDPE
- Pack Size: 10 g
- Net Weight: 10 g
- Gross Weight: 25 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-methylbutanoic acid
- SMILES: CC[C@](NC(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O)(C)C(O)=O
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Medchemexpress LLC H-Val-Gln-OH | 42854-54-6 | 99.82% | 245.28 | 25 MG
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H-Val-Gln-OH is a polypeptide that can be identified through peptide screening. Peptide screening serves as a research tool, primarily pooling active peptides via immunoassay. It is applicable for protein interaction, functional analysis, and epitope screening, particularly in the field of agent research and development.
- Polypeptide identified through peptide screening
- Used for protein interaction studies
- Applicable for functional analysis
- Supports epitope screening
- Useful in agent research and development
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Medchemexpress LLC Val-cit-amide-ph-maytansine | 98.0% | 1055.61 | C51H71ClN8O14 | 5 MG
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Val-cit-amide-ph-maytansine is a maytansine-based drug-linker designed for incorporation into antibody-drug conjugates (ADCs). It contains a valine-citrulline (Val-Cit) cleavable dipeptide linker connected to a maytansine payload via an amide-phenyl spacer, providing a protease-cleavable release mechanism for targeted delivery.
- intended for synthesis of antibody-drug conjugates and drug-linker research
- molecular weight 1055.61
- chemical formula C51H71ClN8O14 (product page) - alternative formula reported in datasheet
- purity reported as 98.01%
- physical form: powder; available in multiple vial sizes (1 mg-200 mg)
- storage: powder -20 °C (up to 3 years) or 4 °C (up to 2 years); in solution -80 °C (up to 6 months)
- solubility: DMSO 100 mg/mL (in vitro); in vivo vehicle formulations reported with solubility ≥ 2.5 mg/mL
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Medchemexpress LLC DBCO-Val-Cit-PABC-PNP | 2994332-18-0 | 97.7% | 859.92 g·mol⁻1 | C46H49N7O10 | 1 MG
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DBCO-Val-Cit-PABC-PNP is a cleavable antibody-drug conjugate (ADC) linker that contains a dibenzocyclooctyne (DBCO) moiety for strain-promoted alkyne-azide cycloaddition (SPAAC). It is used as a click-chemistry reagent to attach payloads to azide-containing molecules and as a Val-Cit-PABC cleavable peptide linker in ADC synthesis.
- Cleavable Val-Cit-PABC peptide linker susceptible to enzyme cleavage.
- DBCO group enables copper-free SPAAC conjugation to azide-containing payloads.
- High reported purity suitable for synthesis and analytical workflows.
- Available in small research pack sizes for conjugation experiments.
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Medchemexpress LLC Aminocaproyl-Val-Cit-PABC-MMAE | 1374407-35-8 | 99.9% | 1236.58 | 25 MG
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Aminocaproyl-Val-Cit-PABC-MMAE is a drug-linker conjugate specifically designed for Antibody-Drug Conjugates (ADCs). It is intended for research use only and is not sold to patients. The product is available in solid form, appearing as a white to off-white powder with a purity of 99.89%. It is categorized under "Antibody-drug Conjugate/ADC Related" and "Drug-Linker Conjugates for ADC" within product classifications.
- High purity: 99.89%
- Specific application: drug-linker conjugate for ADC research
- Available documentation: data sheet, COA, SDS, handling instructions
- Storage recommendations: -20°C, sealed storage, away from moisture; unstable in solutions, freshly prepared is recommended.
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Medchemexpress LLC Val-Cit-PAB-Exatecan | 2227350-99-2 | 99.8% | 840.90 g/mol | C43H49FN8O9 | 50 MG
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Val-Cit-PAB-Exatecan is a linker-drug conjugate composed of the topoisomerase I inhibitor exatecan (DX-8951) linked via a cathepsin-cleavable valine-citrulline p-aminobenzyl carbamate (Val-Cit-PAB) linker, supplied for research use in antibody-drug-conjugate development.
- High purity suitable for research applications.
- Cathepsin-cleavable Val-Cit-PAB linker for intracellular payload release.
- Intended for antibody-drug conjugate synthesis and ADC research.
- Provided as a solid, light yellow to yellow, with analytical data (H NMR, LCMS, RP-HPLC) available.
- Available in multiple milligram sizes for small-scale conjugation work.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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