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ChemicalBook >> CAS DataBase List >>Pasireotide

Pasireotide

CAS No.
396091-73-9
Chemical Name:
Pasireotide
Synonyms
Signifor;SOM 320;SOM 230;PASIREOTIDE;Epifibatide;SOM 230;SOM 320;Pasireotide (SOM-230);Pasireotide Acetate(net);CYCLO((4R)-4-(2-AMINOETHYLCARBAMOYLOXY)-L-PROLYL-L-PHENYLGLYCYL-D-TRYPTOPHYL-L-LYSYL-4-O-BENZYL-L-TYROSYL-L-PHENYLALANYL-);Cyclo[(2S)-2-phenylglycyl-D-tryptophyl-L-lysyl-O-(phenylmethyl)-L-tyrosyl-L-phenylalanyl-(4R)-4-[[[(2-aminoethyl)amino]carbonyl]oxy]-L-prolyl]
CBNumber:
CB02667889
Molecular Formula:
C58H66N10O9
Molecular Weight:
1047.23
MDL Number:
MFCD08067735
MOL File:
396091-73-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 17:32:44
Product description Number Pack Size Price
Pasireotide acetate FP110151 0.5mg $399.3
Pasireotide acetate FP110151 1mg $698.78
Pasireotide acetate FP110151 2mg $1297.72
Pasireotide acetate FP110151 5mg $1996.5
Pasireotide acetate FP110151 10mg $3593.8
More product size

Pasireotide Properties

Boiling point 1351.4±65.0 °C(Predicted)
Density 1.36±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form Powder
pka 11.86±0.46(Predicted)
color White to off-white
Sequence cyclo[Tyr(Bzl)-Phe-Hyp(Bom)-Phg-D-Trp-Lys]
InChIKey VMZMNAABQBOLAK-PHODJXESNA-N
CAS DataBase Reference 396091-73-9
FDA UNII 98H1T17066
NCI Drug Dictionary pasireotide
ATC code H01CB05

Pharmacokinetic data

Protein binding 88%
Excreted unchanged in urine 8%
Volume of distribution >100 Litres
Biological half-life 9-12

SAFETY

Risk and Safety Statements

Pasireotide price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FP110151 Pasireotide acetate 396091-73-9 0.5mg $399.3 2026-06-04 Buy
Biosynth FP110151 Pasireotide acetate 396091-73-9 1mg $698.78 2026-06-04 Buy
Biosynth FP110151 Pasireotide acetate 396091-73-9 2mg $1297.72 2026-06-04 Buy
Biosynth FP110151 Pasireotide acetate 396091-73-9 5mg $1996.5 2026-06-04 Buy
Biosynth FP110151 Pasireotide acetate 396091-73-9 10mg $3593.8 2026-06-04 Buy
Product number Packaging Price Buy
FP110151 0.5mg $399.3 Buy
FP110151 1mg $698.78 Buy
FP110151 2mg $1297.72 Buy
FP110151 5mg $1996.5 Buy
FP110151 10mg $3593.8 Buy

Pasireotide Chemical Properties,Uses,Production

Description

In April 2012, the European Commission approved pasireotide for the treatment of Cushing’s Disease (CD) in adult patients who have not responded to surgical interventionor forwhomsurgery is not anoption.Pasireotide was approved for the same indication by the US FDA in December of 2012. Pasireotide (also known as SOM230) is a cyclohexapeptide that acts as a somatostatin analogue to inhibit the release of ACTH. Somatostatins are cyclic peptides of 14 and 28 amino acids that play animportant role inregulating endocrineandexocrine release inmany tissues through an inhibitory mechanism. There are five known subtypes of somatostatin receptors (SSTRs). Natural somatostatins bind with high affinity to all five subtypes, however, their therapeutic use is limited by rapid degradation in plasma. Pasireotide arose fromefforts to identify a somatostatinmimetic with long-lasting inhibitory effects. Starting with a 14-amino acid somatostatin peptide, a systematic alanine scan revealed residues that were essential for receptor sub-type binding, including key b-turn regions and adjacent residues. Placing the key structural elements as unnatural amino acids in a cyclohexapeptide backbone gave pasireotide.

Originator

Novartis (Switzerland)

Uses

Pasireotide can be used in biological study of long-term treatment of Cushing''s disease with pasireotide, 5-yr results from open-label extension study of Phase III trial.

Definition

ChEBI: Pasireotide is a six-membered homodetic cyclic peptide composed from L-phenylglycyl, D-tryptophyl, L-lysyl, O-benzyl-L-tyrosyl, L-phenylalanyl and modified L-hydroxyproline residues joined in sequence. A somatostatin analogue with pharmacologic properties mimicking those of the natural hormone somatostatin; used (as its diaspartate salt) for treatment of Cushing's disease. It has a role as an antineoplastic agent. It is a homodetic cyclic peptide and a peptide hormone. It is a conjugate base of a pasireotide(2+).

brand name

Signifor

Clinical Use

Pasireotide, also known as SOM230, is a cyclic, hexameric peptide developed by Novartis which exhibits somatostatin-like activity as an antisecretory agent used in the treatment of Cushing’s disease. Pasireotide activates a broad range of somatostatin receptors, and in particular displays a significantly higher binding affinity for somatostatin receptors 1, 3, and 5 than its competitor somatostatin-mimic octreotide in vitro, as well as a comparable binding affinity for somatostatin receptor 2. Pasireotide is more potent than somatostatin in inhibiting the secretion of human growth hormone (HGH), glucagon, and insulin.

Side effects

The Side Effects of Pasireotide: Headache, hair loss, dizziness, diarrhea, gas, bloating, constipation, muscle pain, swelling of arms/legs, and redness/pain/swelling/itching/bleeding at injection site may occur.

Synthesis

The synthesis of pasireotide is relatively straightforward, given that the chemical entity is a cyclic peptide. The most likely scalable route closely mimics that described by the discovery authors involving a series of conventional couplings and deprotection steps to arrive at a linear peptide which then underwent sequential release from solid support, macrocyclization, and a global deprotection step.

Synthesis_396091-73-9


Beginning from (2S,4R)-4-hydroxyproline methyl ester (110) in the scheme above, this pyrrolidine nitrogen was first Fmoc-protected in 85% yield followed by treatment with trisphosgene and N-Boc diaminoethane to provide the prolino carbamate shown in 49% yield over the two step sequence after a recrystallization with ethyl acetate.
Next, commercially available Fmoc-Tyr(Bzl)-O-CH2-Ph(3-OCH3)-O-CH2-SASRIN157 resin (112) was used as starting material in a manually operated reactor and carried through a standard protocol consisting of repetitive cycles of N|á deprotection (piperidine/DMF, 2:8), repeated washings with DMF, and coupling using DIC/HOBT in DMF (Schemes 2 and 3). The following amino acid derivatives were sequentially coupled: Fmoc-Lys(Boc)-OH, Fmoc-D-Trp(Boc)-OH, Fmoc-PhG-OH, proline derivative 111 above, and finally Fmoc-Phe-OH. Couplings were continued or repeated until complete disappearance of residual amino groups as monitored with a ninhydrin stain test. Before cleavage of the protected linear peptide from its resin support, the Fmoc group was removed. After washings with dichloromethane, the peptide resin was transferred into a column and the peptide fragment was cleaved from solid support upon subjection to 2% TFA in dichloromethane. The eluate was immediately neutralized with a saturated NaHCO3 solution which resulted in the side chain protected fragment 119 (the Scheme) was obtained in 93% homogeneity and cyclized without further purification. For cyclization, the linear fragment was dissolved in DMF, treated with DIPEA, and then 1.5 equiv of diphenylphosphoryl azide which resulted in the protected cyclized product obtained in good yield. For complete deprotection, the residue was dissolved at 0 C in aqueous TFA, and the mixture was stirred at this temperature for 30 min. The product was then precipitated with ether containing ca. 10 equiv of HCl, then filtered and washed with ether, and finally dried. The entire sequence produced pasireotide (XVIII) in 20% yield from resin-bound 112.

Drug interactions

Potentially hazardous interactions with other drugs
Antifungals: avoid with ketoconazole.
Ciclosporin: possibly reduces ciclosporin concentration.

Metabolism

Pasireotide is metabolically highly stable and in vitro data show that pasireotide is not a substrate, inhibitor or inducer of any major enzymes of CYP450. In healthy volunteers, pasireotide is mainly found in the unchanged form in plasma, urine and faeces.
Pasireotide is eliminated mainly by hepatic clearance and is mostly found, unchanged, in the faeces (48%) and urine.

Pasireotide Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 139)Suppliers
Supplier Tel Email Country ProdList Advantage
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8615965530500 nickzhang@hangyubiotech.com China 9945 58
Nantong Guangyuan Chemicl Co,Ltd
+undefined17712220823 admin@guyunchem.com China 615 58
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10403 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19936 58
Shanghai Longyu Biotechnology Co., Ltd.
info@longyupharma.com China 2430 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
TopScience Biochemical
00852-68527855 info@itopbiochem.com China Hong Kong 902 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
Neostar United (Changzhou) Industrial Co., Ltd.
+86-0519-85551759 +8613506123987 marketing1@neostarunited.com China 8828 58

Related articles

  • Pasireotide for Cushing's disease
  • Pasireotide is a man-made protein that is similar to a hormone in the body called somatostatin. Pasireotide is used to treat ....
  • Apr 29,2022

View Lastest Price from Pasireotide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Pasireotide pictures 2026-07-24 Pasireotide
396091-73-9
1g 98%min 1000g WUHAN FORTUNA CHEMICAL CO., LTD
PASIREOTIDE pictures 2026-07-06 PASIREOTIDE
396091-73-9
$70.00-700.00 10kg 0.99 20tons Zibo Hangyu Biotechnology Development Co., Ltd
Pasireotide pictures 2026-06-08 Pasireotide
1kg 99% 1 Jinan Ruitong Biotech Co., Ltd.
  • Pasireotide pictures
  • Pasireotide
    396091-73-9
  • $0.00
  • 98%min
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • PASIREOTIDE pictures
  • PASIREOTIDE
    396091-73-9
  • $70.00-700.00
  • 0.99
  • Zibo Hangyu Biotechnology Development Co., Ltd
PASIREOTIDE Cyclo[(2S)-2-phenylglycyl-D-tryptophyl-L-lysyl-O-(phenylmethyl)-L-tyrosyl-L-phenylalanyl-(4R)-4-[[[(2-aminoethyl)amino]carbonyl]oxy]-L-prolyl] SOM 230 SOM 320 [(3S,6S,9S,12R,15S,18S,20R)-9-(4-aminobutyl)-3-benzyl-12-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-15-phenyl-6-[(4-phenylmethoxyphenyl)methyl]-1,4,7,10,13,16-hexazabicyclo[16.3.0]henicosan-20-yl] N-(2-aminoethyl)carbamate SOM 230;SOM 320 CYCLO((4R)-4-(2-AMINOETHYLCARBAMOYLOXY)-L-PROLYL-L-PHENYLGLYCYL-D-TRYPTOPHYL-L-LYSYL-4-O-BENZYL-L-TYROSYL-L-PHENYLALANYL-) Pasireotide Acetate(net) Pasireotide (SOM-230) Epifibatide Signifor 396091-73-9 C58H66N10O9
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