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Bombesin

From Wikipedia, the free encyclopedia
Bombesin
Names
Other names
Pyr-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C71H110N24O18S/c1-34(2)24-47(92-62(105)43(14-11-22-79-71(76)77)89-64(107)45(15-18-52(72)96)90-63(106)44-17-20-55(99)85-44)61(104)81-31-56(100)87-51(28-54(74)98)69(112)91-46(16-19-53(73)97)65(108)94-49(26-38-29-80-41-13-10-9-12-40(38)41)66(109)84-37(7)60(103)95-58(36(5)6)70(113)82-32-57(101)86-50(27-39-30-78-33-83-39)68(111)93-48(25-35(3)4)67(110)88-42(59(75)102)21-23-114-8/h9-10,12-13,29-30,33-37,42-51,58,80H,11,14-28,31-32H2,1-8H3,(H2,72,96)(H2,73,97)(H2,74,98)(H2,75,102)(H,78,83)(H,81,104)(H,82,113)(H,84,109)(H,85,99)(H,86,101)(H,87,100)(H,88,110)(H,89,107)(H,90,106)(H,91,112)(H,92,105)(H,93,111)(H,94,108)(H,95,103)(H4,76,77,79)/t37-,42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,58-/m0/s1 ☒N
    Key: QXZBMSIDSOZZHK-DOPDSADYSA-N ☒N
  • InChI=1/C71H110N24O18S/c1-34(2)24-47(92-62(105)43(14-11-22-79-71(76)77)89-64(107)45(15-18-52(72)96)90-63(106)44-17-20-55(99)85-44)61(104)81-31-56(100)87-51(28-54(74)98)69(112)91-46(16-19-53(73)97)65(108)94-49(26-38-29-80-41-13-10-9-12-40(38)41)66(109)84-37(7)60(103)95-58(36(5)6)70(113)82-32-57(101)86-50(27-39-30-78-33-83-39)68(111)93-48(25-35(3)4)67(110)88-42(59(75)102)21-23-114-8/h9-10,12-13,29-30,33-37,42-51,58,80H,11,14-28,31-32H2,1-8H3,(H2,72,96)(H2,73,97)(H2,74,98)(H2,75,102)(H,78,83)(H,81,104)(H,82,113)(H,84,109)(H,85,99)(H,86,101)(H,87,100)(H,88,110)(H,89,107)(H,90,106)(H,91,112)(H,92,105)(H,93,111)(H,94,108)(H,95,103)(H4,76,77,79)/t37-,42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,58-/m0/s1
    Key: QXZBMSIDSOZZHK-DOPDSADYBX
  • [H]/N=C(\N)/NCCC[C@@H](C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](Cc1c[nH]c2c1cccc2)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](Cc3c[nH]cn3)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@@H]4CCC(=O)N4
Properties
C71H110N24O18S
Molar mass1619.85
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Bombesin is a 14-amino acidpeptide[1] originally isolated from theskin of theEuropean fire-bellied toad (Bombina bombina)[2] byVittorio Erspameret al. and named after its source.[3] It has two knownhomologs inmammals calledneuromedin B andgastrin-releasing peptide. It stimulatesgastrin release fromG cells. It activates three differentG-protein-coupledreceptors known as BBR1, -2, and -3.[4] It also activates these receptors in thebrain. Together withcholecystokinin, it is the second major source ofnegative feedback signals that stop eating behaviour.[5]

Bombesin is also atumor marker for small cell carcinoma of lung, gastric cancer, pancreatic cancer, andneuroblastoma.[6]

Receptors

[edit]

TheanuranBB4 receptorhomologue is termedfrog BB4 (fBB4).[3] Iwabuchiet al. 2003 discovered achicken (Gallus domesticus) receptor which is homologous to both themammalian BB3 and fBB4 and so they named itchBRS-3.5.[3]

Effects

[edit]

Erspamer 1988 finds bombesin has a similar effect on the chicken to ranatensin, unreliably increasing or decreasing blood pressure.[7]

See also

[edit]

References

[edit]
  1. ^Gonzalez N, Moody TW, Igarashi H, Ito T, Jensen RT (February 2008)."Bombesin-related peptides and their receptors: recent advances in their role in physiology and disease states".Current Opinion in Endocrinology, Diabetes and Obesity.15 (1):58–64.doi:10.1097/MED.0b013e3282f3709b.PMC 2631407.PMID 18185064.
  2. ^
  3. ^abcJensen, R. T.; Battey, J. F.; Spindel, E. R.; Benya, R. V. (2007-11-30)."International Union of Pharmacology. LXVIII. Mammalian Bombesin Receptors: Nomenclature, Distribution, Pharmacology, Signaling, and Functions in Normal and Disease States".Pharmacological Reviews.60 (1).American Society for Pharmacology & Experimental Therapeutics (ASPET):1–42.doi:10.1124/pr.107.07108.ISSN 0031-6997.PMC 2517428.PMID 18055507.NIHMSID 45053.
  4. ^Weber HC (February 2009). "Regulation and signaling of human bombesin receptors and their biological effects".Current Opinion in Endocrinology, Diabetes and Obesity.16 (1):66–71.doi:10.1097/med.0b013e32831cf5aa.PMID 19115523.S2CID 45482442.
  5. ^Yamada K, Wada E, Wada K (November 2000). "Bombesin-like peptides: studies on food intake and social behaviour with receptor knock-out mice".Annals of Medicine.32 (8):519–29.doi:10.3109/07853890008998831.PMID 11127929.S2CID 24431961.
  6. ^Ohlsson B, Fredäng N, Axelson J (December 1999). "The effect of bombesin, cholecystokinin, gastrin, and their antagonists on proliferation of pancreatic cancer cell lines".Scandinavian Journal of Gastroenterology.34 (12):1224–9.doi:10.1080/003655299750024742.PMID 10636070.
  7. ^
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