Unsaturated hydrocarbons
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Filtered Search Results
Medchemexpress LLC NO2A-Butyne | 2089035-56-1 | 98.0% | 354.40 | C16H26N4O5 | 10mg
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NO2A-Butyneis a bifunctional chelator (Bifunctional Chelator BFC) and a macrocyclic NOTA derivative used for tumor pre-targeting NO2A-Butyne can be used for conjugation of peptides and radionuclides
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Aobchem AOBCHEM
5001006494 PHENYLMETHYL 3-CYCLOPENTENE-1-
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Medchemexpress LLC Bpin-Cyclohexene-COOEt | 1049004-32-1 | 280.17 | 1 G
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Bpin-Cyclohexene-COOEt is a PROTAC linker belonging to the PEG class. This compound can be utilized in the synthesis of PROTAC molecules.
- PROTAC linker
- Belongs to the PEG class
- Suitable for synthesizing PROTAC molecules
- Purity of ≥97.0% by NMR
- Appears as a colorless to light yellow liquid
- Recommended storage at -20°C for 3 years (unstable in solutions, fresh preparation recommended)
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Aobchem Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 5g
Phenylmethyl 3-cyclopentene-1-carboxylate | 95% | CAS 130762-09-3 | C13H14O2 | 5g
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Cayman Chemical cis-Vaccenic Acid, Purity: ≥98%, CAS: 506-17-2, 50 mg
An ω-7 fatty acid; induces differentiation of, and γ-globin synthesis in, K562 and JK-1 cells, as well as isolated sickle cell TMbmEPSCs
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Medchemexpress LLC VE-821 | 1232410-49-9 | 99.7% | 368.41 | 50 MG
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VE-821 is a potent ATP-competitive inhibitor of ATR, with Ki/IC50 values of 13 nM/26 nM. It demonstrates excellent selectivity for ATR, showing minimal cross-reactivity against related PIKKs such as ATM, DNA-PK, mTOR, and PI3Kγ.
- Shows minimal cross-reactivity against related PIKKs ATM, DNA-PK, mTOR, and PI3Kγ
- Significantly enhances the sensitivity of PSN-1, MiaPaCa-2, and primary PancM pancreatic cancer cells to radiation and Gemcitabine
- ATR inhibition by VE-821 leads to inhibition of radiation-induced G2/M arrest in cancer cells
- Inhibits phosphorylation of Chk1 (Ser 345) in PSN-1 and MiaPaCa-2 cells after treatment with Gemcitabine, radiation, or both
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eMolecules 2243-98-3 | 1-Undecyne | MFCD00015063 | 10g
Ambeed | [11-Biphenyl]-3-ylboronic acid | 1g | 490498337 | A118718 | 5122-95-2 | MFCD01318102 | 198.030 | C12H11BO2
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eMolecules 7-Tetradecene | 10374-74-0 | MFCD00009550 | 1g
Oakwood Chemicals | 7-Tetradecene | 1g | 480151123 | 099796 | | 10374-74-0 | MFCD00009550 | 196.378 | C14H28
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eMolecules 3-CYCLOPENTENE-1-OL 10G
5000163297 3-CYCLOPENTENE-1-OL 10G
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eMolecules 3-CYCLOPENTENE-1-OL 5G
5000163554 3-CYCLOPENTENE-1-OL 5G
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eMolecules 287944-10-9 | Cyclopentene-1-boronic acid, pinacol ester | Combi-Blocks | MFCD08669391 | 194.080 | C11H19BO2 | 95.000 | CC1(C)OB(OC1(C)C)C1=CCCC1 | 100g | 357557212
Cyclopentene-1-boronic acid, pinacol ester | Combi-Blocks | 287944-10-9 | MFCD08669391 | 194.080 | C11H19BO2 | 95.000 | CC1(C)OB(OC1(C)C)C1=CCCC1 | 100g | 357557212
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Aobchem 4-(Methoxycarbonyl)cyclohexene-1-boronic acid pinacol ester | ≥95% | CAS 151075-20-6 | C14H23BO4 | 1g
4-(Methoxycarbonyl)cyclohexene-1-boronic acid pinacol ester | ≥95% | CAS 151075-20-6 | C14H23BO4 | 1g
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Medchemexpress LLC Di-591 | 2245887-38-9 | 98.1% | 585.80 g/mol | C31H47N5O4S | 25MG
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DI-591 is a cell-permeable small-molecule inhibitor of the DCN1-UBC12 interaction that binds DCN1 and DCN2 with high affinity (Ki ≈ 12 nM and 10.4 nM) and selectively inhibits neddylation of cullin 3. It is supplied at research-grade purity for biochemical and cellular studies of neddylation and ubiquitin-proteasome pathway regulation.
- High-affinity binding to DCN1 and DCN2 (Ki ≈ 12 nM, 10.4 nM)
- Selective inhibition of cullin 3 neddylation
- Cell-permeable for cellular assays
- High purity (~98.1%) suitable for research use
- Molecular weight 585.80 g/mol; formula C31H47N5O4S
- Available in multiple milligram pack sizes for laboratory studies
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Medchemexpress LLC PG-931 | 667430-81-1 | 99.8% | 1180.40 | 10 MG
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PG-931 is an analog of SHU 9119 and a potent, selective melanocortin 4 (MC4) receptor agonist. This compound has demonstrated the ability to reverse hemorrhagic shock and prevent multiple organ damage in vivo.
- Potent melanocortin 4 (MC4) receptor agonist with an IC50 of 0.58 nM.
- More selective for MC4R than for hMC3R (IC50=55 nM) or hMC5R (IC50=2.4 nM).
- Can reverse hemorrhagic shock and prevent multiple organ damage in vivo.
- Exhibits anti-shock effects at nanomolar doses.
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BOC SCIENCES 3,7,11-TRIMETHYL-1-DODECENE-1G
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3,7,11-Trimethyl-1-dodecene, 1G
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