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BGC > Product Search > Bavachinin A | 19879-30-2
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Suppliers for CAS

19879-30-2



 

Properties

CAS   19879-30-2 
Formula   C21H22O4 

Structure

7 Registered suppliers


Dayang Chem (Hangzhou) Co.,Ltd. P.R.China
Leap Chem Co., Ltd P.R.China
Hangzhou Lingrui Chemical Co., Ltd. P.R.China
Molecular Formula: C21H22O4
Molecular Weight: 338.4
Hazard Symbols: N
UN Number: UN 3077 9 / PGIII
WGKGermany: 3
Skyrun Industrial Co., Ltd. P.R.China
Molecular Formula: C21H22O4
Molecular Weight: 338.4
Hazard Symbols: N
UN Number: UN 3077 9 / PGIII
WGKGermany: 3
BOC Sciences USA
Chemos GmbH & Co. KG Germany
Description :
Bavachinin is a natural compound isolated from the Chinese herb Fructus Psoraleae. Bavachinin has potent anti-angiogenic activity in vitro and in vivo. Bavachinin inhibited increases in HIF-1α activity in human KB carcinoma (HeLa cell derivative) and human HOS osteosarcoma cells under hypoxia in a concentration-dependent manner, probably by enhancing the interaction between von Hippel-Lindau (VHL) and HIF-1α. It significantly inhibited Th2 cytokine production, including IL-4, IL-5 and IL-13. Notably, this compound almost completely blocked inflammation in the ovalbumin (OVA)-sensitized animal asthma model.
  • Molecular Weight :338.4
  • Boiling Point :537.1±50.0 °C at 760 mmHg
  • Melting Point :139-145°C
  • Purity :> 98%
Molecular Formula :
C21H22O4
Canonical SMILES :
CC(=CCC1=C(C=C2C(=C1)C(=O)CC(O2)C3=CC=C(C=C3)O)OC)C
InChI :
InChI=1S/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3/t20-/m0/s1
InChIKey :
VOCGSQHKPZSIKB-FQEVSTJZSA-N
Appearance :
Powder
Application :
antiinflammatory; antipyretic; analgesic
Synonyms :
7-O-Methylbavachin; Bavachinin A
More details are to be found here
BuGuCh & Partners Germany
Description :
Bavachinin is a natural compound isolated from the Chinese herb Fructus Psoraleae. Bavachinin has potent anti-angiogenic activity in vitro and in vivo. Bavachinin inhibited increases in HIF-1α activity in human KB carcinoma (HeLa cell derivative) and human HOS osteosarcoma cells under hypoxia in a concentration-dependent manner, probably by enhancing the interaction between von Hippel-Lindau (VHL) and HIF-1α. It significantly inhibited Th2 cytokine production, including IL-4, IL-5 and IL-13. Notably, this compound almost completely blocked inflammation in the ovalbumin (OVA)-sensitized animal asthma model.
  • Molecular Weight :338.4
  • Boiling Point :537.1±50.0 °C at 760 mmHg
  • Melting Point :139-145°C
  • Purity :> 98%
Molecular Formula :
C21H22O4
Canonical SMILES :
CC(=CCC1=C(C=C2C(=C1)C(=O)CC(O2)C3=CC=C(C=C3)O)OC)C
InChI :
InChI=1S/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3/t20-/m0/s1
InChIKey :
VOCGSQHKPZSIKB-FQEVSTJZSA-N
Appearance :
Powder
Application :
antiinflammatory; antipyretic; analgesic
Synonyms :
7-O-Methylbavachin; Bavachinin A
More details are to be found here

Detailed information on the suppliers of Bavachinin A

Properties:

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