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ChemicalBook >> CAS DataBase List >>BFH772

BFH772

CAS No.
890128-81-1
Chemical Name:
BFH772
Synonyms
BFH772;CS-2412;Bfh-722;BFH-772; BFH 772;BFH772, 10 mM in DMSO;6-((6-(Hydroxymethyl)pyrimidin-4-yl)oxy)-N-(3-(trifluoromethyl)phenyl)-1-naphthamide;inhibit,BFH 772,VEGFR,BFH-772,BFH772,Vascular endothelial growth factor receptor,Inhibitor;1-Naphthalenecarboxamide, 6-[[6-(hydroxymethyl)-4-pyrimidinyl]oxy]-N-[3-(trifluoromethyl)phenyl]-
CBNumber:
CB03147777
Molecular Formula:
C23H16F3N3O3
Molecular Weight:
439.39
MDL Number:
MFCD30534392
MOL File:
890128-81-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 17:37:17
Product description Number Pack Size Price
BFH772 ≥95% 21386 1mg $42
BFH772 ≥95% 21386 5mg $183
BFH772 ≥95% 21386 10mg $322
BFH772 ≥95% 21386 25mg $653
BFH-772 21386 1mg $38
More product size

BFH772 Properties

Boiling point 541.2±50.0 °C(Predicted)
Density 1.432±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form A crystalline solid
pka 12.65±0.70(Predicted)
color White to off-white
FDA UNII T1IV236CVP

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
NFPA 704
0
2 0

BFH772 price More Price(56)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21386 BFH772 ≥95% 890128-81-1 1mg $42 2026-04-30 Buy
Cayman Chemical 21386 BFH772 ≥95% 890128-81-1 5mg $183 2026-04-30 Buy
Cayman Chemical 21386 BFH772 ≥95% 890128-81-1 10mg $322 2026-04-30 Buy
Cayman Chemical 21386 BFH772 ≥95% 890128-81-1 25mg $653 2026-04-30 Buy
Cayman Chemical 21386 BFH-772 890128-81-1 1mg $38 2024-03-01 Buy
Product number Packaging Price Buy
21386 1mg $42 Buy
21386 5mg $183 Buy
21386 10mg $322 Buy
21386 25mg $653 Buy
21386 1mg $38 Buy

BFH772 Chemical Properties,Uses,Production

Description

BFH772 is an inhibitor of VEGF receptor 2 (VEGFR2; IC50 = 0.0027 μM for the human receptor). It is selective for human VEGFR2 over mouse VEGFR2 and human VEGFR1 and VEGFR3 (IC50s = 1.5, 1.7, and 1.1 μM, respectively), as well as 40-fold selective over B-RAF, RET, and Tie2. BFH772 inhibits VEGF-induced proliferation of human umbilical vein endothelial cells (HUVECs; IC50 = <0.01 nM). It inhibits VEGF-induced increases in tissue weight and Tie2 levels in an angiogenesis chamber implant model in mice when administered at doses of 1 and 3 mg/kg per day. BFH772 (3 mg/kg per day) inhibits primary tumor and metastasis growth in a B16 melanoma mouse model.

Uses

BFH772 is a potent oral VEGFR2 inhibitor, which is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM[1].

in vitro

bfh772 was highly effective at targeting vegfr2 kinase, however, lost 500-fold potency on flk-1, flt-1, and flt-4. bfh772 also targeted b-raf, ret, and tie-2, albeit with at least 40-fold lower potency. bfh772 inhibited the ligand induced autophosphorylation of ret, pdgfr, and kit kinases. bfh772 was selective against the kinases of egfr, erbb2, ins-r, and igf-1r and against the cytoplasmic bcr-abl kinase [1].

in vivo

the dose response curves of bfh772 at 0.3, 1, and 3 mg/kg showed that even at the lowest concentrations, this naphthalene-1-carboxamide inhibited vegf induced tissue weight and tie-2 levels but only reached statistical significance at 1 mg/kg and above. moreover, bfh772 at 3 mg/kg orally dosed once per day could potently inhibit melanoma growth (54-90% for primary tumor and 71-96% for metastasis tumor) when compared with control ratios [1].

IC 50

3 nm

References

[1] bold g, et al. a novel potent oral series of vegfr2 inhibitors abrogate tumor growth by inhibiting angiogenesis. j med chem. 2016 jan 14;59(1):132-46.
[2] http://adisinsight. springer.com/trials/700244037

BFH772 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 79)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
SHANGHAI T&W PHARMACEUTICAL CO., LTD.
+86-021-61551413 +8618813727289 contact@trustwe.com China 5745 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32466 58
BOC Sciences
16314854226; +16314854226 inquiry@bocsci.com United States 19853 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471; sales@sarms4muscle.com China 10473 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6391 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49734 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39037 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11680 58

View Lastest Price from BFH772 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
BFH772 pictures 2026-04-27 BFH772
890128-81-1
$38.00-105.00 99.89% 10g TargetMol Chemicals Inc.
BFH772 pictures 2019-12-23 BFH772
890128-81-1
$1.00 1g 99.99% 200kg Career Henan Chemical Co
  • BFH772 pictures
  • BFH772
    890128-81-1
  • $38.00-105.00
  • 99.89%
  • TargetMol Chemicals Inc.
  • BFH772 pictures
  • BFH772
    890128-81-1
  • $1.00
  • 99.99%
  • Career Henan Chemical Co

BFH772 Spectrum

BFH772 Bfh-722 CS-2412 BFH-772; BFH 772 1-Naphthalenecarboxamide, 6-[[6-(hydroxymethyl)-4-pyrimidinyl]oxy]-N-[3-(trifluoromethyl)phenyl]- 6-((6-(Hydroxymethyl)pyrimidin-4-yl)oxy)-N-(3-(trifluoromethyl)phenyl)-1-naphthamide inhibit,BFH 772,VEGFR,BFH-772,BFH772,Vascular endothelial growth factor receptor,Inhibitor BFH772, 10 mM in DMSO 890128-81-1
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