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Cantharidin 98.0+%, TCI America™
CAS: 56-25-7 Molecular Formula: C10H12O4 Molecular Weight (g/mol): 196.202 MDL Number: MFCD00134968 InChI Key: DHZBEENLJMYSHQ-XCVPVQRUSA-N Synonym: cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p PubChem CID: 5944 ChEBI: CHEBI:64213 SMILES: CC12C3CCC(C1(C(=O)OC2=O)C)O3
| PubChem CID | 5944 |
|---|---|
| CAS | 56-25-7 |
| Molecular Weight (g/mol) | 196.202 |
| ChEBI | CHEBI:64213 |
| MDL Number | MFCD00134968 |
| SMILES | CC12C3CCC(C1(C(=O)OC2=O)C)O3 |
| Synonym | cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p |
| InChI Key | DHZBEENLJMYSHQ-XCVPVQRUSA-N |
| Molecular Formula | C10H12O4 |
Cantharidin, 98%, Thermo Scientific Chemicals
CAS: 56-25-7 Molecular Formula: C10H12O4 Molecular Weight (g/mol): 196.202 MDL Number: MFCD00134968 InChI Key: DHZBEENLJMYSHQ-XCVPVQRUSA-N Synonym: cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p PubChem CID: 5944 ChEBI: CHEBI:64213 SMILES: CC12C3CCC(C1(C(=O)OC2=O)C)O3
| PubChem CID | 5944 |
|---|---|
| CAS | 56-25-7 |
| Molecular Weight (g/mol) | 196.202 |
| ChEBI | CHEBI:64213 |
| MDL Number | MFCD00134968 |
| SMILES | CC12C3CCC(C1(C(=O)OC2=O)C)O3 |
| Synonym | cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p |
| InChI Key | DHZBEENLJMYSHQ-XCVPVQRUSA-N |
| Molecular Formula | C10H12O4 |
exo-7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic anhydride, 98%
CAS: 29745-04-8 Molecular Formula: C8H8O4 Molecular Weight (g/mol): 168.148 MDL Number: MFCD00213361 InChI Key: JAABVEXCGCXWRR-GUCUJZIJSA-N Synonym: exo-3,6-Epoxyhexahydrophthalic anhydride; Norcantharadin PubChem CID: 12251906 SMILES: C1CC2C3C(C1O2)C(=O)OC3=O
| PubChem CID | 12251906 |
|---|---|
| CAS | 29745-04-8 |
| Molecular Weight (g/mol) | 168.148 |
| MDL Number | MFCD00213361 |
| SMILES | C1CC2C3C(C1O2)C(=O)OC3=O |
| Synonym | exo-3,6-Epoxyhexahydrophthalic anhydride; Norcantharadin |
| InChI Key | JAABVEXCGCXWRR-GUCUJZIJSA-N |
| Molecular Formula | C8H8O4 |
Norcantharidin 98.0+%, TCI America™
CAS: 29745-04-8 Molecular Formula: C8H8O4 Molecular Weight (g/mol): 168.148 MDL Number: MFCD00213361 InChI Key: JAABVEXCGCXWRR-GUCUJZIJSA-N Synonym: exo-3,6-Epoxyhexahydrophthalic Anhydride, exo-7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Anhydride PubChem CID: 12251906 SMILES: C1CC2C3C(C1O2)C(=O)OC3=O
| PubChem CID | 12251906 |
|---|---|
| CAS | 29745-04-8 |
| Molecular Weight (g/mol) | 168.148 |
| MDL Number | MFCD00213361 |
| SMILES | C1CC2C3C(C1O2)C(=O)OC3=O |
| Synonym | exo-3,6-Epoxyhexahydrophthalic Anhydride, exo-7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Anhydride |
| InChI Key | JAABVEXCGCXWRR-GUCUJZIJSA-N |
| Molecular Formula | C8H8O4 |
4,9,11-Trioxatetracyclo[5.3.1.0(2,6).0(8,10)]undecan-3-one 98.0+%, TCI America™
CAS: 632339-23-2 Molecular Formula: C8H8O4 Molecular Weight (g/mol): 168.15 MDL Number: MFCD10566937 InChI Key: UAFDSOCDQRHNCL-UHFFFAOYNA-N Synonym: 2,6-Epoxy-2,2a,5,5a,6,6a-hexahydrooxireno[f]isobenzofuran-3(1aH)-one PubChem CID: 20632532 IUPAC Name: 4,9,11-trioxatetracyclo[5.3.1.0²,⁶.0⁸,¹⁰]undecan-3-one SMILES: O=C1OCC2C3OC(C4OC34)C12
| PubChem CID | 20632532 |
|---|---|
| CAS | 632339-23-2 |
| Molecular Weight (g/mol) | 168.15 |
| MDL Number | MFCD10566937 |
| SMILES | O=C1OCC2C3OC(C4OC34)C12 |
| Synonym | 2,6-Epoxy-2,2a,5,5a,6,6a-hexahydrooxireno[f]isobenzofuran-3(1aH)-one |
| IUPAC Name | 4,9,11-trioxatetracyclo[5.3.1.0²,⁶.0⁸,¹⁰]undecan-3-one |
| InChI Key | UAFDSOCDQRHNCL-UHFFFAOYNA-N |
| Molecular Formula | C8H8O4 |
4,10-Dioxatricyclo[5.2.1.0(2,6)]decan-8-en-3-one 97.0+%, TCI America™
CAS: 72150-22-2 Molecular Formula: C8H8O3 Molecular Weight (g/mol): 152.149 InChI Key: KIAQKKYOUVIGII-UHFFFAOYSA-N Synonym: 4,7-Epoxy-3a,4,7,7a-tetrahydroisobenzofuran-1(3H)-one PubChem CID: 331417 SMILES: C1C2C3C=CC(C2C(=O)O1)O3
| PubChem CID | 331417 |
|---|---|
| CAS | 72150-22-2 |
| Molecular Weight (g/mol) | 152.149 |
| SMILES | C1C2C3C=CC(C2C(=O)O1)O3 |
| Synonym | 4,7-Epoxy-3a,4,7,7a-tetrahydroisobenzofuran-1(3H)-one |
| InChI Key | KIAQKKYOUVIGII-UHFFFAOYSA-N |
| Molecular Formula | C8H8O3 |
MEDCHEMEXPRESS LLC DINOTEFURAN 50MG
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501874186 DINOTEFURAN 50MG
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Medchemexpress LLC HY-15005 100mg , PSI-7977 GS 7977;sofosbuvir CAS:1190307-88-0 Purity:98%
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Medchemexpress, HY-15005 100mg PSI-7977 GS 7977;sofosbuvir CAS:1190307-88-0 Formula:C22H29FN3O9P EC50: 92±5 nM (HCV) Purity:98% PSI-7977 is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus ( HCV ) activity. 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 HY-N0432 5mg Medchemexpress, Astragaloside I CAS:84680-75-1 Purity:>98%
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Medchemexpress, HY-N0432 5mg Astragaloside I CAS:84680-75-1 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 HY-N0433 5mg Medchemexpress, Astragaloside II CAS:84676-89-1 Purity:>98%
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Medchemexpress, HY-N0433 5mg Astragaloside II CAS:84676-89-1 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 HY-15005 10mg Medchemexpress, Sofosbuvir CAS:1190307-88-0 Purity:>98%
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Medchemexpress, HY-15005 10mg Sofosbuvir CAS:1190307-88-0 Sofosbuvir (GS-7977) is an HCV RNA replication inhibitor with an EC50 of 92 nM. 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 HY-B0192A 10mg Medchemexpress, Alfuzosin (hydrochloride) CAS:81403-68-1 Purity:>98%
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Medchemexpress, HY-B0192A 10mg Alfuzosin (hydrochloride) CAS:81403-68-1 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 3-Methyluridine | 2140-69-4 | 99.1% | 258.23 | 10 MG
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3-Methyluridine | 2140-69-4 | 99.1% | 258.23 | 10 MG
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Apexbio Technology LLC Cantharidin 20mg
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Cantharidin is a naturally occurring terpenoid compound known to function as a potent and selective inhibitor of serine/threonine protein phosphatases particularly protein phosphatase 2A (PP2A) and protein phosphatase 1 (PP1) By inhibiting these enzymes cantharidin disrupts the regulation of numerous cellular processes including cell cycle progression apoptosis and signal transduction pathways This molecule has been widely utilized in research to investigate phosphatase-mediated signaling mechanisms and to explore its potential role in modulating cancer cell proliferation and death Cantharidin serves as a valuable tool for dissecting the functional roles of PP1 and PP2A in various biological systems
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Medchemexpress LLC 3-Methyluridine (N3-Methyluridine) | 2140-69-4 | 99.1% | 258.23 | 100 MG
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3-Methyluridine (m3U; N3-Methyluridine) is a methylated nucleotide found in ribosomal RNA (rRNA). It introduces a methyl group at the N3 position of uracil, regulating ribosome function and affecting RNA secondary structure stability and base pairing. This compound is a key raw material for synthesizing modified nucleotides and constructing RNA oligonucleotides with methylation modifications.
- Methylated nucleotide found in ribosomal RNA
- Targets specific base sites of RNA molecules
- Regulates ribosome function
- Affects RNA secondary structure stability and base pairing ability
- Used for synthesizing modified nucleotides
- Used for constructing RNA oligonucleotides with methylation modifications
- Supports studies on the impact of RNA methylation on gene expression and drug resistance
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