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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 |
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 |
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 |
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 |
SAPPHIRE NORTH AMERICA ATPGAMMAS 50MG
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NC3626801 ATPGAMMAS 50MG
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eMolecules 15291-77-7 | Medchem Express | Ginkgolide B | 25mg | 728132878 | HY-N0784 | 424.402 | C20H24O10
Ambeed | (3AR8aS)-2[2-(diphenylphosphanyl)phenyl]-3a8a-dihydroindane[12-d]oxazole | 50mg | 532083693 | A1264386 | 212312-33-9 | 419.464 | C28H22NOP
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Alkali Scientific Cantharidin, 150 Milligrams
Cantharidin is a potent bioactive compound widely used in laboratory research for its enzyme inhibitory properties. This chemical is often used to study cellular processes and to investigate the mechanisms of enzyme inhibition. In particular, cantharidin has been studied for its effects on protein phosphatases, which play crucial roles in cell signaling and regulation. The 150mg format makes it suitable for laboratory experiments requiring precise doses of cantharidin, particularly in studies related to biochemistry, pharmacology, and toxicology. This product is commonly used by researchers exploring the effects of enzyme inhibition on cellular pathways, making it a valuable tool for biochemical investigations.
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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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Medchemexpress LLC Liguiritigenin-7-O-D-apiosyl-4'-O-D-glucoside | 199796-12-8 | 5 MG
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Liguiritigenin-7-O-D-apiosyl-4'-O-D-glucoside is a flavanone glycoside isolated from Glycyrrhizia inflata.
- Isolated from Glycyrrhizia inflata.
- Purity: 99.56%.
- For research use only.
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Medchemexpress LLC HY-101978 10mg Medchemexpress, CPI-444 CAS:1202402-40-1 Purity:>98%
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Medchemexpress, HY-101978 10mg CPI-444 CAS:1202402-40-1 CPI-444 (V81444) is a potent, orally active and selective adenosine A2A receptor (A2AR) antagonist, which induces antitumor responses. 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 2'-Deoxycytidine hydrochloride | 3992-42-5 | 100.0% | 263.68 | 500 MG
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2'-Deoxycytidine hydrochloride is an orally effective inhibitor of nucleic acid biosynthesis enzymes. It works by competing with these enzymes and nucleoside transporters, which helps to reduce the toxicity associated with cytarabine. This compound is also utilized in research related to L1210 lymphoblastic leukemia.
- Orally effective nucleic acid biosynthesis enzyme inhibitor.
- Competes with nucleoside transporters.
- Reduces cytarabine toxicity.
- Applicable in L1210 lymphoblastic leukemia research.
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eMolecules 20311-51-7 | Medchem Express | Solamargine | 5mg | 446274563 | HY-N0069 | MFCD30207844 | 868.071 | C45H73NO15
Ambeed | 4-(4-(4455-Tetramethyl-132-dioxaborolan-2-yl)phenethyl)morpholine | 100mg | 534566539 | A138141 | 364794-81-0 | MFCD04440855 | 317.240 | C18H28BNO3
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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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