Terpene lactones
Rotenone, ≥97%, MP Biomedicals™
CAS: 83-79-4 Molecular Formula: C23H22O6 Molecular Weight (g/mol): 394.423 InChI Key: JUVIOZPCNVVQFO-HBGVWJBISA-N Synonym: rotenone,dactinol,paraderil,--rotenone,tubatoxin,barbasco,--cis-rotenone,derrin,derris,cube root PubChem CID: 6758 ChEBI: CHEBI:28201 SMILES: CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC
Rotenone 95.0+%, TCI America™
CAS: 83-79-4 Molecular Formula: C23H22O6 Molecular Weight (g/mol): 394.423 MDL Number: MFCD09025614 InChI Key: JUVIOZPCNVVQFO-HBGVWJBISA-N Synonym: rotenone,dactinol,paraderil,--rotenone,tubatoxin,barbasco,--cis-rotenone,derrin,derris,cube root PubChem CID: 6758 ChEBI: CHEBI:28201 SMILES: CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC
Medchemexpress LLC HY-N0038 5mg Medchemexpress, Alantolactone CAS:546-43-0 Purity:>98%
Medchemexpress, HY-N0038 5mg Alantolactone CAS:546-43-0 Alantolactone is a selective STAT3 inhibitor, with potent anticancer activity. 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.
Selleck Chemical LLC Alantolactone
Alantolactone a naturally occurring eudesmane-type sesquiterpene lactone (SL) could induce activin/SMAD3 signaling and disrupt Cripto-1/activin receptor type II A interaction
Apexbio Technology LLC Alantolactone 546-43-0 20mg
Alantolactone (CAS 546-43-0) is a sesquiterpene lactone primarily isolated from the roots of Inula helenium L and leaves of Inula grandis This compound is known to modulate multiple cellular pathways including the inhibition of NF- B signaling and the induction of apoptosis via reactive oxygen species (ROS) generation Alantolactone has demonstrated anti-inflammatory and antiproliferative activities in various in vitro models making it a valuable tool for investigating molecular mechanisms underlying inflammation and cancer The compound should be stored in a sealed container under cool and dry conditions for optimal stability
Medchemexpress LLC HY-B1761 500mg Medchemexpress, Santonin CAS:481-06-1 Purity:>98%
Medchemexpress, HY-B1761 500mg Santonin CAS:481-06-1 Santonin is an active principle of the plant Artemisia cina, which is formely used to treat worms. 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.
TARGETMOL CHEMICALS INC ALANTOLACTONE 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Alantolactone (Inula camphor)(Alant camphor) a sesquiterpene lactone has potential activity against triple-negative breast Y MDA-MB-231 cells by suppressing the signal transducer and activator of transcription 3 (STAT3) signaling pathway. purity: 99%
Selleck Chemical LLC a-santonin S3999-25mg
-santonin a naturally occurring sesquiterpene lactone is a potent antiparasitic agent
Selleck Chemical LLC Alantolactone
Alantolactone a naturally occurring eudesmane-type sesquiterpene lactone (SL) could induce activin/SMAD3 signaling and disrupt Cripto-1/activin receptor type II A interaction
Selleck Chemical LLC Alantolactone
Alantolactone a naturally occurring eudesmane-type sesquiterpene lactone (SL) could induce activin/SMAD3 signaling and disrupt Cripto-1/activin receptor type II A interaction
Medchemexpress LLC Alantolactone | 546-43-0 | MFCD00274568 | 99.9% | 232.32 g/mol | C15H20O2 | 10 MG
Alantolactone is a sesquiterpene lactone used in research as a selective STAT3 inhibitor with potent anticancer activity; it induces apoptosis in cancer cells and is supplied as a solid with characterized purity, solubility, and storage recommendations suitable for in vitro and in vivo studies.
- Selective STAT3 inhibitor suitable for cancer biology research.
- High purity (≈99.9%) supports reproducible results.
- Soluble in DMSO at high concentrations for in vitro assays.
- Available in small pack sizes (including 10 MG) for pilot studies.
- Recommended storage conditions provided for long-term stability.
Alantolactone, Tocris Bioscience™
CAS: 546-43-0 Molecular Formula: C15H20O2 Molecular Weight (g/mol): 232.32 MDL Number: MFCD00274568 InChI Key: PXOYOCNNSUAQNS-AGNJHWRGSA-N Synonym: alantolactone,helenine,eupatal,alant camphor,inula camphor,helenin,elecampane camphor,unii-m7gsn5q1m6,m7gsn5q1m6,3ar,5s,8ar,9ar-5,8a-dimethyl-3-methylidene-3a,5,6,7,8,8a,9,9a-octahydronaphtho 2,3-b furan-2 3h-one PubChem CID: 72724 ChEBI: CHEBI:2540 IUPAC Name: (3aR,5S,8aR,9aR)-5,8a-dimethyl-3-methylidene-2H,3H,3aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one SMILES: C[C@H]1CCC[C@]2(C)C[C@H]3OC(=O)C(=C)[C@H]3C=C12
Thermo Scientific Chemicals Rotenone 97%, Thermo Scientific™
CAS: 83-79-4 Molecular Formula: C23H22O6 Molecular Weight (g/mol): 394.423 InChI Key: JUVIOZPCNVVQFO-HBGVWJBISA-N Synonym: rotenone,dactinol,paraderil,--rotenone,tubatoxin,barbasco,--cis-rotenone,derrin,derris,cube root PubChem CID: 6758 ChEBI: CHEBI:28201 SMILES: CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC
MP Biomedicals, Inc Santonin, MP Biomedicals™
CAS: 481-06-1 Molecular Formula: C15H18O3 Molecular Weight (g/mol): 246.31 MDL Number: MFCD00135865 InChI Key: XJHDMGJURBVLLE-BOCCBSBMSA-N Synonym: santonin,alpha-santonin,--alpha-santonin,santoninic anhydride,--santonin,unii-1vl8j38ero,semenen,--santonine,1vl8j38ero,santoninum PubChem CID: 221071 ChEBI: CHEBI:16363 IUPAC Name: (3S,3aS,5aS,9bS)-3,5a,9-trimethyl-2H,3H,3aH,4H,5H,5aH,8H,9bH-naphtho[1,2-b]furan-2,8-dione SMILES: C[C@H]1[C@@H]2CC[C@@]3(C)C=CC(=O)C(C)=C3[C@H]2OC1=O
Santonin 98.0+%, TCI America™
CAS: 481-06-1 Molecular Formula: C15H18O3 Molecular Weight (g/mol): 246.31 MDL Number: MFCD00135865 InChI Key: XJHDMGJURBVLLE-BOCCBSBMSA-N Synonym: santonin,alpha-santonin,--alpha-santonin,santoninic anhydride,--santonin,unii-1vl8j38ero,semenen,--santonine,1vl8j38ero,santoninum PubChem CID: 221071 ChEBI: CHEBI:16363 IUPAC Name: (3S,3aS,5aS,9bS)-3,5a,9-trimethyl-2H,3H,3aH,4H,5H,5aH,8H,9bH-naphtho[1,2-b]furan-2,8-dione SMILES: C[C@H]1[C@@H]2CC[C@@]3(C)C=CC(=O)C(C)=C3[C@H]2OC1=O