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Tetrahydrocoptisine

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Li, W.; Huang, H.; Zhang, Y.; Fan, T.; Liu, X.; Xing, W.; Niu, X. (2013). "Anti-inflammatory effect of tetrahydrocoptisine from Corydalis impatiens is a function of possible inhibition of TNF-α, IL-6 and NO production in lipopolysaccharide-stimulated peritoneal macrophages through inhibiting NF-κB
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Except where otherwise noted, data are given for materials in their
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5,6,7,8-Tetrahydro-(1,3)dioxolo(4,5-g)isoquinolines
148: 59: 225:C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 8: 201: 103: 15: 168: 330: 222: 197: 7: 139: 123: 14: 341:European Journal of Pharmacology 258: 252: 22: 289:(at 25 °C , 100 kPa). 339:activation and MAPK pathway". 261: 246: 1: 353:10.1016/j.ejphar.2013.06.017 397: 283: 233: 213: 43: 35: 30: 21: 17:Tetrahydrocoptisine 318:Corydalis impatiens 305:Tetrahydrocoptisine 279: g·mol 18: 293:Infobox references 16: 301:Chemical compound 299: 298: 182:CompTox Dashboard 85:Interactive image 388: 365: 364: 335: 278: 263: 260: 254: 248: 241:Chemical formula 206: 205: 190: 188: 172: 152: 141: 127: 107: 87: 63: 26: 19: 396: 395: 391: 390: 389: 387: 386: 385: 371: 370: 369: 368: 337: 336: 332: 327: 307:(also known as 302: 295: 290: 276: 266: 257: 251: 243: 229: 226: 221: 220: 209: 191: 184: 175: 155: 142: 130: 110: 90: 77: 66: 53: 39: 12: 11: 5: 394: 392: 384: 383: 373: 372: 367: 366: 347:(1–3): 62–71. 329: 328: 326: 323: 315:isolated from 300: 297: 296: 291: 287:standard state 284: 281: 280: 274: 268: 267: 264: 255: 249: 244: 239: 236: 235: 231: 230: 228: 227: 224: 216: 215: 214: 211: 210: 208: 207: 199:DTXSID50904180 194: 192: 180: 177: 176: 174: 173: 165: 163: 157: 156: 154: 153: 145: 143: 135: 132: 131: 129: 128: 120: 118: 112: 111: 109: 108: 100: 98: 92: 91: 89: 88: 80: 78: 71: 68: 67: 65: 64: 56: 54: 49: 46: 45: 41: 40: 37: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 393: 382: 379: 378: 376: 362: 358: 354: 350: 346: 342: 334: 331: 324: 322: 320: 319: 314: 310: 306: 294: 288: 282: 275: 273: 270: 269: 245: 242: 238: 237: 232: 223: 219: 212: 204: 200: 196: 195: 193: 183: 179: 178: 171: 167: 166: 164: 162: 159: 158: 151: 147: 146: 144: 138: 134: 133: 126: 122: 121: 119: 117: 114: 113: 106: 102: 101: 99: 97: 94: 93: 86: 82: 81: 79: 75: 70: 69: 62: 58: 57: 55: 52: 48: 47: 42: 34: 29: 25: 20: 344: 340: 333: 316: 308: 304: 303: 44:Identifiers 36:Other names 234:Properties 325:References 272:Molar mass 170:J0JS75Q12Z 96:ChemSpider 72:3D model ( 51:CAS Number 309:stylopine 61:4312-32-7 38:Stylopine 375:Category 361:23810685 313:alkaloid 311:) is an 277:323.348 137:PubChem 359:  218:SMILES 125:C05175 31:Names 74:JSmol 357:PMID 161:UNII 150:6770 116:KEGG 105:6512 349:doi 345:715 187:EPA 140:CID 377:: 355:. 343:. 321:. 256:17 250:19 363:. 351:: 265:4 262:O 259:N 253:H 247:C 189:) 185:( 76:)

Index


CAS Number
4312-32-7
JSmol
Interactive image
ChemSpider
6512
KEGG
C05175
PubChem
6770
UNII
J0JS75Q12Z
CompTox Dashboard
DTXSID50904180
Edit this at Wikidata
SMILES
Chemical formula
Molar mass
standard state
Infobox references
alkaloid
Corydalis impatiens
doi
10.1016/j.ejphar.2013.06.017
PMID
23810685
Category
5,6,7,8-Tetrahydro-(1,3)dioxolo(4,5-g)isoquinolines

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