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atrasentan

atrasentan Suppliers list
Company Name: Huawei Zhihe Pharmaceutical Technology (Shanghai) Co., Ltd.  Gold
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atrasentan manufacturers

  • atrasentan
  • atrasentan pictures
  • 2026-06-30
  • CAS:173937-91-2
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1000kg
  • atrasentan
  • atrasentan pictures
  • 2020-01-10
  • CAS:173937-91-2
  • Min. Order: 1KG
  • Purity: 98%; 99%
  • Supply Ability: 500g;1kg; 25kg
atrasentan Basic information
Product Name:atrasentan
Synonyms:atrasentan;(+)-A 127722;A-147627;(2R,3R,4S)-4-(1,3-Benzodioxol-5-yl)-1-[2-(dibutylamino)-2-oxoethyl]-2-(4-methoxyphenyl)-3-pyrrolidinecarboxylic acid;(2S,3S,4R)-4-(1,3-BENZODIOXOL-5-YL)-1-[2-(DIBUTYLAMINO)-2-OXOETHYL]-2-(4-METHOXYPHENYL)PYRROLIDINE-3-CARBOXYLIC ACID;A127722, CID 5310990;Atrasentan (ABT-627);(+)-A 127722; ABT-627; A 127722; ABT 627
CAS:173937-91-2
MF:C29H38N2O6
MW:510.62
EINECS:
Product Categories:API
Mol File:173937-91-2.mol
atrasentan Structure
atrasentan Chemical Properties
Melting point 122-124°
Boiling point 659.4±55.0 °C(Predicted)
density 1.188±0.06 g/cm3(Predicted)
storage temp. -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka3.49±0.60(Predicted)
color Off-White
InChIKeyMOTJMGVDPWRKOC-QPVYNBJUSA-N
SMILESN1(CC(N(CCCC)CCCC)=O)C[C@H](C2=CC=C3OCOC3=C2)[C@@H](C(O)=O)[C@@H]1C1=CC=C(OC)C=C1
Safety Information
MSDS Information
atrasentan Usage And Synthesis
UsesPalliative treatment of bone pain due to metastatic prostate cancer and disease progression (endothelin (ETA) receptor antagonist).
UsesAtrasentan is a selective antagonist of the endothelin-A (ETA) receptor and binds selectively to the ETA receptor, which may result in inhibition of endothelin-induced angiogenesis and tumor cell proliferation.
DefinitionChEBI: Atrasentan is a member of pyrrolidines.
in vivo

Atrasentan (3 mg/kg, p.o.) inhibits the pressor response induced by big endothelin-1 (1 nmol/kg) in pithed rats[1]. Aatrasentan (ABT-627, 10 mg/kg, i.p.) as well as Taxotere alone inhibited the C4-2b tumor growth within the bone environment to some extent in the SCID-hu model[2].

atrasentan Preparation Products And Raw materials
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tert-Butyl ethyl ether Aspartame Dioxopromethazine HCl Benzo[a]pyrene Selenium dioxide 1,4-Dioxane 2-(2-Aminoethylamino)ethanol atrasentan