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Surufatinib

CAS No.
1308672-74-3
Chemical Name:
Surufatinib
Synonyms
HMPL012;CS-2346;HMPL-012;KDR-IN-1;EOS-61498;Surufatinib;Surufatinib(HPML-012);Sulfatinib, 10 mM in DMSO;HMPL-012;SURUFATINIB;HMPL012;N-(2-(DIMETHYLAMINO)ETHYL)-1-(3-((4-((2-METHYL-1H-INDOL-5-YL)OXY)PYRIMIDIN-2-YL)AMINO)PHENYL)METHANE
CBNumber:
CB72711244
Molecular Formula:
C24H28N6O3S
Molecular Weight:
480.58
MDL Number:
MOL File:
1308672-74-3.mol
MSDS File:
SDS
Last updated:2026-04-17 13:05:51
Product description Number Pack Size Price
Sulfatinib S688948 1mg $60
Sulfatinib S688948 10mg $340
Sulfatinib 98.01% CS-5949 100mg $450
Sulfatinib 98.01% CS-5949 5mg $90
Sulfatinib 98.01% CS-5949 10mg $120
More product size

Surufatinib Properties

Boiling point 712.9±70.0 °C(Predicted)
Density 1.332±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:98.0(Max Conc. mg/mL);203.92(Max Conc. mM)
form A solid
pka 5.22±0.40(Predicted)
color White to off-white
InChIKey TTZSNFLLYPYKIL-UHFFFAOYSA-N
SMILES C1(CS(NCCN(C)C)(=O)=O)=CC=CC(NC2=NC=CC(OC3C=CC4=C(C=3)C=C(C)N4)=N2)=C1
FDA UNII B2K5L1L8S9

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

Surufatinib price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC S688948 Sulfatinib 1308672-74-3 1mg $60 2021-12-16 Buy
TRC S688948 Sulfatinib 1308672-74-3 10mg $340 2021-12-16 Buy
ChemScene CS-5949 Sulfatinib 98.01% 1308672-74-3 100mg $450 2021-12-16 Buy
ChemScene CS-5949 Sulfatinib 98.01% 1308672-74-3 5mg $90 2021-12-16 Buy
ChemScene CS-5949 Sulfatinib 98.01% 1308672-74-3 10mg $120 2021-12-16 Buy
Product number Packaging Price Buy
S688948 1mg $60 Buy
S688948 10mg $340 Buy
CS-5949 100mg $450 Buy
CS-5949 5mg $90 Buy
CS-5949 10mg $120 Buy

Surufatinib Chemical Properties,Uses,Production

Uses

Sulfatinib is used in pharmaceutical compositions comprising of micronized drug.

Mechanism of action

Surufatinib can inhibit multiple targets related to angiogenesis and tumor growth, including VEGFR, FGFR1 and CSF-1R.

Synthesis

Treatment of sulfonyl chloride 358 at room temperature using triethylamine and 2,2,2-trifluoroethanol (TFE) as solvents followed by hydrogenation afforded aniline 360. Exposure of 360 to DBU under microwave conditions generated an intermediate sulfinyl group. This intermediate sulfinyl group subsequently underwent nucleophilic attack by a commercial diamine, of which diamine 361 afforded the desired sulfonamide 362. Dichloropyrimidine 363 underwent a substitution reaction with hydroxyindole 364 to afford diaryl ether 365. Diaryl ether 365 then underwent a second substitution reaction with amine 362 under acidic conditions. Exposure of the product to a base in aqueous solution ultimately afforded surufatinib in 50% yield.
Surufatinib synthesis

in vivo

In animal studies, a single oral dosing of Sulfatinib inhibits VEGF stimulated VEGFR2 phosphorylation in lung tissues of nude mice in an exposure-dependent manner. Furthermore, elevation of FGF23 levels in plasma 24 hours post dosing suggests suppression of FGFR signaling. Sulfatinib demonstrates potent tumor growth inhibition in multiple human xenograft models and decreases CD31 expression remarkably, suggesting strong inhibition on angiogenesis through VEGFR and FGFR signaling. In a syngeneic murine colon cancer model CT-26, Sulfatinib demonstrates moderate tumor growth inhibition after single agent treatment[1]. After oral dosing of 10 mg/kg, the AUC and Cmax are 397 ng/mL and 138ng/mL in the mouse, respectively[1].

IC 50

VEGFR1; VEGFR2; VEGFR3; FGFR1; CSF1R

1071105-16-2
1094797-87-1
1308672-74-3
Synthesis of Surufatinib from 5-((2-chloropyriMidin-4-yl)oxy)-2-Methyl-1H-indole and 1-(3-aMinophenyl)-N-(2-(diMethylaMino)ethyl)MethanesulfonaMide

Surufatinib Preparation Products And Raw materials

Global( 91)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
Jinan Carbotang Biotech Co.,Ltd.
+8615866703830 figo.gao@foxmail.com China 8497 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32467 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10236 58
HONG KONG IPURE BIOLOGY CO.,LIMITED
86 18062405514 18062405514 ada@ipurechemical.com CHINA 3461 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6312 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6391 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 market18@leapchem.com China 24597 58
Nantong HI-FUTURE Biology Co., Ltd.
+undefined18051384581 sales@chemhifuture.com China 3135 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8467 58

Related articles

  • Synthesis of Surufatinib
  • Surufatinib is synthesised from dichloropyrimidine and hydroxyindole by substitution reaction. This process requires the parti....
  • Jan 5,2024

View Lastest Price from Surufatinib manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sulfatinib pictures 2026-04-17 Sulfatinib
1308672-74-3
US $39.00-97.00 / mg 99.97% 10g TargetMol Chemicals Inc.
  • Sulfatinib pictures
  • Sulfatinib
    1308672-74-3
  • US $39.00-97.00 / mg
  • 99.97%
  • TargetMol Chemicals Inc.
N-(2-(diMethylaMino)ethyl)-1-(3-((4-((2-Methyl-1H-indol-5-yl)oxy)pyriMidin-2-yl)aMino)phenyl)MethanesulfonaMide KDR-IN-1 EOS-61498 HMPL012 HMPL-012 HMPL-012;SURUFATINIB;HMPL012 Surufatinib CS-2346 N-(2-(DIMETHYLAMINO)ETHYL)-1-(3-((4-((2-METHYL-1H-INDOL-5-YL)OXY)PYRIMIDIN-2-YL)AMINO)PHENYL)METHANE Benzenemethanesulfonamide, N-[2-(dimethylamino)ethyl]-3-[[4-[(2-methyl-1H-indol-5-yl)oxy]-2-pyrimidinyl]amino]- Surufatinib(HPML-012) Sulfatinib, 10 mM in DMSO 1308672-74-3