Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
Basic Description
| Synonyms | Lumicolchicine|gamma-Lumicolchicine|6901-13-9|Lumicolchicine gamma|beta-Lumicolchicine|6901-14-0|NSC56233|[7S-(7alpha,7bbeta,10abeta)]-N-(5,6,7,7b,8,10a-hexahydro-1,2,3,9-tetramethoxy-8-oxobenzo[a]cyclopenta[3,4]cyclobuta[1,2-c]cyclohepten-7-yl)acetamide| |
|---|---|
| Storage Temp | Room temperature |
| Shipped In | Normal |
Associated Targets
CBX1 Tbio Chromobox protein homolog 1 0 Activities
GMNN Tbio Geminin 0 Activities
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
Names and Identifiers
| IUPAC Name | N-[(10S,12R,16S)-3,4,5,14-tetramethoxy-13-oxo-10-tetracyclo[9.5.0.02,7.012,16]hexadeca-1(11),2,4,6,14-pentaenyl]acetamide |
|---|---|
| INCHI | InChI=1S/C22H25NO6/c1-10(24)23-13-7-6-11-8-15(27-3)21(28-4)22(29-5)16(11)17-12-9-14(26-2)20(25)18(12)19(13)17/h8-9,12-13,18H,6-7H2,1-5H3,(H,23,24)/t12-,13+,18-/m1/s1 |
| InChi Key | VKPVZFOUXUQJMW-FHSNZYRGSA-N |
| Canonical SMILES | CC(=O)NC1CCC2=CC(=C(C(=C2C3=C1C4C3C=C(C4=O)OC)OC)OC)OC |
| Isomeric SMILES | CC(=O)N[C@H]1CCC2=CC(=C(C(=C2C3=C1[C@H]4[C@@H]3C=C(C4=O)OC)OC)OC)OC |
| PubChem CID | 244898 |
| UN Number | 1544 |
| Packing Group | I |
| Molecular Weight | 399.44 |
Certificates
Certificate of Analysis(COA)
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Chemical and Physical Properties
| Refractive Index | n20D1.60 (Predicted) |
|---|---|
| Boil Point(°C) | ~623.2° C at 760 mmHg (Predicted) |
| Melt Point(°C) | ~238.93° C (Predicted) |
Safety and Hazards(GHS)
| Pictogram(s) | GHS07 |
|---|---|
| Signal | Warning |
| Hazard Statements | H302:Harmful if swallowed |
| Precautionary Statements | P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help. |
| Class | 6.1 |