Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C20H25NO2 |
| Molecular Weight | 311.418 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(CC[C@H]3[C@@H]4CC=C[C@@]4(C)CC[C@H]23)C=C1C(N)=O
InChI
InChIKey=YQJWOUQGXATDAE-ACNBBOPNSA-N
InChI=1S/C20H25NO2/c1-20-8-3-4-17(20)14-6-5-12-10-16(19(21)22)18(23-2)11-15(12)13(14)7-9-20/h3,8,10-11,13-14,17H,4-7,9H2,1-2H3,(H2,21,22)/t13-,14+,17-,20-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| ENMD-1198, a new analogue of 2-methoxyestradiol, displays both antiangiogenic and vascular-disrupting properties. | 2010-05 |
|
| Synthesis, antiproliferative, and pharmacokinetic properties of 3- and 17-double-modified analogs of 2-methoxyestradiol. | 2009-11-01 |
|
| ENMD-1198, a novel tubulin-binding agent reduces HIF-1alpha and STAT3 activity in human hepatocellular carcinoma(HCC) cells, and inhibits growth and vascularization in vivo. | 2008-07-23 |
|
| A comparison of two orally bioavailable anti-cancer agents, IRC-110160 and STX140. | 2008-07-18 |
|
| Significant antitumor activity in vivo following treatment with the microtubule agent ENMD-1198. | 2008-06 |
Patents
| Name | Type | Language | ||
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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DB05959
Created by
admin on Mon Mar 31 18:28:28 GMT 2025 , Edited by admin on Mon Mar 31 18:28:28 GMT 2025
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DTXSID40235571
Created by
admin on Mon Mar 31 18:28:28 GMT 2025 , Edited by admin on Mon Mar 31 18:28:28 GMT 2025
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864668-87-1
Created by
admin on Mon Mar 31 18:28:28 GMT 2025 , Edited by admin on Mon Mar 31 18:28:28 GMT 2025
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11483754
Created by
admin on Mon Mar 31 18:28:28 GMT 2025 , Edited by admin on Mon Mar 31 18:28:28 GMT 2025
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760O4GJB9O
Created by
admin on Mon Mar 31 18:28:28 GMT 2025 , Edited by admin on Mon Mar 31 18:28:28 GMT 2025
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PRIMARY |
ACTIVE MOIETY