Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Palmitic acid
Price: Check
Purity: 98.0%
Stocking Period: 10 Day
Contact: Yang
Email: sales@echemcloud.com

Henan Tianfu Chemical Co., Ltd.
China
Product Name: Somatostatin
Price: $Inquiry/1kg $Inquiry/25kg $Inquiry/1000kg $Inquiry/10ton
Purity: 99.0%
Stocking Period: Inquiry
Contact: Anson
Email: info@tianfuchem.com

51110-01-1

51110-01-1 structure

51110-01-1 structure

Name: Somatostatin
Chemical Name: Somatostatin
CAS Number: 51110-01-1
Molecular Formula: C₇₆H₁₀₄N₁₈O₁₉S₂
Molecular Weight: 1637.878
Catalog: API Hormone and endocrine-regulating drugs other
Create Date: 2018-03-03 08:00:00
Modify Date: 2026-06-30 11:51:47
Somatostatin is a tetradecapeptide which can suppress the growth hormone (GH) secretion and control the pituitary hormone secretion in human CNS.

Name	Somatostatin
Synonyms	Somatostatin Acetate(net) H-ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS-OH (COUPLED TO KLH) SS-14 SOMATOSTATIN, SHE Somatostatin panhibin H-ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS-OH OWTH HORMONE RELEASE INHIBITING FACTOR (HUMAN, OVINE, PORCINE, RAT, MOUSE) 2ACOH 6H2O SOMATOSTATIN-14 (COUPLED TO KLH) Stilamin GIF (HUMAN, OVINE, PORCINE, RAT, MOUSE) Anti-Somatostatin, N-Terminal antibody produced in rabbit ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-PHE-THR-SER-CYS-OH L-Alanylglycyl-L-cysteinyl-L-lysyl-L-asparaginyl-L-phenylalanyl-L-phenylalanyl-L-tryptophyl-L-lysyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-cysteine Cyclic (3®14) Disulfide SRIF Aminopan SOMATOSTATIN, CYCLIC Somatostain SRIF (HUMAN, OVINE, PORCINE, RAT, MOUSE) OWTH HORMONE RELEASE INHIBITING FACTOR SOMATOSTATIN (HUMAN, OVINE, PORCINE, RAT, MOUSE) 2ACOH 6H2O H-ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS-OH (COUPLED TO BSA) Somatostatin //BP panhibin AKNFFWKTFTSC (DISULFIDE BRIDGE: ) GH-RIF SRIF-A SOMATOSTATIN-14 OWTH HORMONE RELEASE INHIBITING FACTOR (HUMAN, OVINE, PORCINE, RAT, MOUSE) C76H104N18O19S2 SOMATOSTATIN [GIF] AKNFFWKTFTSC growth hormone inhibiting hormone SOMATOSTATIN [TYR1] L-Alanyl-N-[(4R,7S,10S,13S,16S,19S,22S,25S,28S,31S,34S,37R)-19,34-bis(4-aminobutyl)-31-(2-amino-2-oxoethyl)-13,25,28-tribenzyl-4-carboxy-10-[(1S)-1-hydroxyethyl]-16-(1-hydroxyethyl)-7-(hydroxymethyl)-22-(1H-indol-3-ylmethyl)-6,9,12,15,18,21,24,27,30,33,36-undecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35-undecaazacyclooctatriacontan-37-yl]glycinamide SOMATOTROPIN RELEASE INHIBITING FACTOR GIF (HUMAN, OVINE, PORCINE, RAT, MOUSE) 2ACOH 6H2O ay24910 CCRIS Somatofalk ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS somatotropin release inhibiting factor Somatostatina SOMATOSTATIN [D-TRP8] SRIF (HUMAN, OVINE, PORCINE, RAT, MOUSE) 2ACOH 6H2O SOMATOSTATIN ACETATE Somatostatin, Endogenous neuroptide 15-28-Somatostatin-28 SOMATOTROPIN RELEASE INHIBITING FACTOR (HUMAN, OVINE, PORCINE, RAT, MOUSE) ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS 2ACOH 6H2O Modustatina H-ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS-OH (DISULFIDE BRIDGE: ) SOMATOTROPIN RELEASE INHIBITING FACTOR (HUMAN, OVINE, PORCINE, RAT, MOUSE) 2ACOH 6H2O EINECS 254-186-5 SOMATOSTATIN (HUMAN, OVINE, PORCINE, RAT, MOUSE) H-ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS-OH, CYS3,14, CYCLIC SOMATOSTATIN-14 (COUPLED TO BSA) Somatostatin Acetate SOMATOSTATIN-14 (REDUCED) 19,34-bis(4-aminobutyl)-31-(2-amino-2-oxoethyl)-37-[[2-(2-aminopropanoylamino)acetyl]amino]-13,25,28-tribenzyl-10,16-bis(1-hydroxyethyl)-7-(hydroxymethyl)-22-(1~{H}-indol-3-ylmethyl)-6,9,12,15,18,21,24,27,30,33,36-undecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35-undecazacyclooctatriacontane-4-cboxylic acid L-Alanyl-N-[(4R,7S,10S,13S,16S,19S,22S,25S,28S,31S,34S,37R)-19,34-bis(4-aminobutyl)-31-(2-amino-2-oxoethyl)-13,25,28-tribenzyl-4-carboxy-10,16-bis[(1R)-1-hydroxyethyl]-7-(hydroxymethyl)-22-(1H-indol-3-ylmethyl)-6,9,12,15,18,21,24,27,30,33,36-undecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35-undecaazacyclooctatriacontan-37-yl]glycinamide

Description	Somatostatin is a tetradecapeptide which can suppress the growth hormone (GH) secretion and control the pituitary hormone secretion in human CNS.
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Cancer Research Areas >> Endocrinology Research Areas >> Neurological Disease Peptides
In Vitro	Somatostatin is a tetradecapeptide which can suppress the growth hormone (GH) secretion and control the pituitary hormone secretion in human CNS. Somatostatin has two biologically active forms: the predominant form is the 14 amino-acid long Somatostatin-14 while the more potent form is the amino-terminus extended Somatostatin-28. The biological roles of the two Somatostatin isoforms very strongly overlap and the relative proportions of Somatostatin-14 to Somatostatin-28 vary between different tissues. Somatostatin can reduce adhesion of carcinosarcoma cells to the blood vessels and thus attenuate the metastatic potential of these tumours. Somatostatin can also inhibit monocyte chemotactic migration[1].
References	[1]. Msaouel P, et al. Somatostatin and somatostatin receptors: implications for neoplastic growth and cancer biology. Expert Opin Investig Drugs. 2009 Sep;18(9):1297-316.

Density	1.4±0.1 g/cm3
Boiling Point	1970.9±65.0 °C at 760 mmHg
Molecular Formula	C₇₆H₁₀₄N₁₈O₁₉S₂
Molecular Weight	1637.878
Flash Point	1145.7±34.3 °C
Exact Mass	1636.716675
PSA	663.83000
LogP	-4.25
Vapour Pressure	0.0±0.3 mmHg at 25°C
Index of Refraction	1.670
Water Solubility	H2O: 1 mg/mL

CHEMICAL IDENTIFICATION

RTECS NUMBER :: WF8751700

CHEMICAL NAME :: Somatostatin

CAS REGISTRY NUMBER :: 51110-01-1

LAST UPDATED :: 199509

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: 21 mg/kg

TOXIC EFFECTS :: Brain and Coverings - recordings from specific areas of CNS Behavioral - somnolence (general depressed activity)

REFERENCE :: TOLED5 Toxicology Letters. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1977- Volume(issue)/page/year: 17,145,1983

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 33 mg/kg

TOXIC EFFECTS :: Brain and Coverings - recordings from specific areas of CNS Behavioral - somnolence (general depressed activity)

REFERENCE :: TOLED5 Toxicology Letters. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1977- Volume(issue)/page/year: 17,145,1983

Hazard Codes	Xi
Risk Phrases	R36/37/38
Safety Phrases	26-36
WGK Germany	3
RTECS	WF8751700

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.