Fmoc-Hyp(Bom)-OH

Modify Date: 2024-01-02 17:51:01

Fmoc-Hyp(Bom)-OH Structure
Fmoc-Hyp(Bom)-OH structure
Common Name Fmoc-Hyp(Bom)-OH
CAS Number 187223-15-0 Molecular Weight 539.577
Density 1.35±0.1 g/cm3 Boiling Point 749.0±60.0 °C at 760 mmHg
Molecular Formula C28H33N3O8 Melting Point N/A
MSDS N/A Flash Point 406.8±32.9 °C

 Use of Fmoc-Hyp(Bom)-OH


Fmoc-Hyp(Bom)-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Hyp(Bom)-OH is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1]<

 Names

Name fmoc-l-hyp(bom)-oh
Synonym More Synonyms

 Fmoc-Hyp(Bom)-OH Biological Activity

Description Fmoc-Hyp(Bom)-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Hyp(Bom)-OH is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1]<
Related Catalog
Target

Cleavable

In Vitro ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[1]. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[2].
References

[1]. Beck A, et al. Strategies and challenges for the next generation of antibody-drug conjugates. Nat Rev Drug Discov. 2017;16(5):315-337.

[2]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-985.

 Chemical & Physical Properties

Density 1.35±0.1 g/cm3
Boiling Point 749.0±60.0 °C at 760 mmHg
Molecular Formula C28H33N3O8
Molecular Weight 539.577
Flash Point 406.8±32.9 °C
Exact Mass 539.226746
PSA 143.50000
LogP 3.54
Vapour Pressure 0.0±2.6 mmHg at 25°C
Index of Refraction 1.620
Water Solubility Insuluble (1.5E-3 g/L) (25 ºC)

 Synthetic Route

~%

Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: NOVARTIS AG; NOVARTIS PHARMA GMBH Patent: WO2004/52817 A1, 2004 ; Location in patent: Page 19-20 ;

~70%

Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: Lewis, Ian; Bauer, Wilfried; Albert, Rainer; Chandramouli, Nagarajan; Pless, Janos; Weckbecker, Gisbert; Bruns, Christian Journal of Medicinal Chemistry, 2003 , vol. 46, # 12 p. 2334 - 2344

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Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: Lewis, Ian; Bauer, Wilfried; Albert, Rainer; Chandramouli, Nagarajan; Pless, Janos; Weckbecker, Gisbert; Bruns, Christian Journal of Medicinal Chemistry, 2003 , vol. 46, # 12 p. 2334 - 2344

~%

Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: Lewis, Ian; Bauer, Wilfried; Albert, Rainer; Chandramouli, Nagarajan; Pless, Janos; Weckbecker, Gisbert; Bruns, Christian Journal of Medicinal Chemistry, 2003 , vol. 46, # 12 p. 2334 - 2344

~%

Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: Lewis, Ian; Bauer, Wilfried; Albert, Rainer; Chandramouli, Nagarajan; Pless, Janos; Weckbecker, Gisbert; Bruns, Christian Journal of Medicinal Chemistry, 2003 , vol. 46, # 12 p. 2334 - 2344

~%

Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: Lewis, Ian; Bauer, Wilfried; Albert, Rainer; Chandramouli, Nagarajan; Pless, Janos; Weckbecker, Gisbert; Bruns, Christian Journal of Medicinal Chemistry, 2003 , vol. 46, # 12 p. 2334 - 2344

~%

Fmoc-Hyp(Bom)-OH Structure

Fmoc-Hyp(Bom)-OH

CAS#:187223-15-0

Literature: Lewis, Ian; Bauer, Wilfried; Albert, Rainer; Chandramouli, Nagarajan; Pless, Janos; Weckbecker, Gisbert; Bruns, Christian Journal of Medicinal Chemistry, 2003 , vol. 46, # 12 p. 2334 - 2344

 Synonyms

1,2-Pyrrolidinedicarboxylic acid, 4-[[[[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]amino]carbonyl]oxy]-, 1-(9H-fluoren-9-ylmethyl) ester, (2S,4R)-
1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-({[2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)ethyl]carbamoyl}oxy)proline
Fmoc-(2S,4R)-Pro(4-OCO-NH-CH2-CH2-NH-Boc)-OH
1,2-Pyrrolidinedicarboxylic acid, 4-[[[[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]amino]carbonyl]oxy]-, 1-(9H-fluoren-9-ylmethyl) ester
(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-({[2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)ethyl]carbamoyl}oxy)-L-proline
Fmoc-Hyp(Bcc)-OH
Fmoc-(2S,4R)-(4-OCO-NH-CH2-CH2-NH-Boc)-Pro-OH
(2S,4R)-4-[[[[2-[[(1,1-Dimethylethoxy)carbonyl]amino]ethyl]amino]carbonyl]oxy]-1,2-pyrrolidinedicarboxylic acid 1-(9H-fluoren-9-ylmethyl) ester
Fmoc-Hyp(Bom)-OH
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