MedKoo Cat#: 531549 | Name: BIBO3304

Description:

WARNING: This product is for research use only, not for human or veterinary use.

BIBO3304 is a NPY Y1 receptor antagonist (IC50 values are 0.38 and 0.72 nM at human and rat receptors respectively) that displays > 2600-fold selectivity over Y2, Y4 and Y5 receptors. BIBO3304 inhibits NPY- and fasting-induced feeding in vivo following central administration.

Chemical Structure

BIBO3304
BIBO3304
CAS#191868-13-0 (free base)

Theoretical Analysis

MedKoo Cat#: 531549

Name: BIBO3304

CAS#: 191868-13-0 (free base)

Chemical Formula: C29H35N7O3

Exact Mass: 529.2801

Molecular Weight: 529.65

Elemental Analysis: C, 65.76; H, 6.66; N, 18.51; O, 9.06

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
BIBO3304; BIBO 3304; BIBO-3304
IUPAC/Chemical Name
(2R)-N-[[4-[(carbamoylamino)methyl]phenyl]methyl]-5-(diaminomethylideneamino)-2-[[2,2-di(phenyl)acetyl]amino]pentanamide
InChi Key
TVMJSGGZULFVCZ-XMMPIXPASA-N
InChi Code
InChI=1S/C29H35N7O3/c30-28(31)33-17-7-12-24(26(37)34-18-20-13-15-21(16-14-20)19-35-29(32)39)36-27(38)25(22-8-3-1-4-9-22)23-10-5-2-6-11-23/h1-6,8-11,13-16,24-25H,7,12,17-19H2,(H,34,37)(H,36,38)(H4,30,31,33)(H3,32,35,39)/t24-/m1/s1
SMILES Code
O=C(NCC1=CC=C(CNC(N)=O)C=C1)[C@H](NC(C(C2=CC=CC=C2)C3=CC=CC=C3)=O)CCC/N=C(N)/N
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 529.65 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
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PubMed PMID: 24779394; PubMed Central PMCID: PMC4128051. 4: Wierońska JM, Stachowicz K, Kłodzińska A, Smiałowska M, Pilc A. Intraamygdaloid administration of BIBO 3304 increases water intake and extends anxiolytic effects. Pol J Pharmacol. 2004 Nov-Dec;56(6):867-70. PubMed PMID: 15662103. 5: Maric T, Sedki F, Chafetz D, Schoela N, Shalev U. A role for neuropeptide Y Y5 but not the Y1-receptor subtype in food deprivation-induced reinstatement of heroin seeking in the rat. Psychopharmacology (Berl). 2011 Dec;218(4):693-701. doi: 10.1007/s00213-011-2362-9. Epub 2011 Jun 1. PubMed PMID: 21629996. 6: Cohen S, Vainer E, Matar MA, Kozlovsky N, Kaplan Z, Zohar J, Mathé AA, Cohen H. Diurnal fluctuations in HPA and neuropeptide Y-ergic systems underlie differences in vulnerability to traumatic stress responses at different zeitgeber times. Neuropsychopharmacology. 2015 Feb;40(3):774-90. doi: 10.1038/npp.2014.257. Epub 2014 Sep 22. PubMed PMID: 25241802; PubMed Central PMCID: PMC4289967. 7: Keller M, Schindler L, Bernhardt G, Buschauer A. Toward Labeled Argininamide-Type NPY Y1 Receptor Antagonists: Identification of a Favorable Propionylation Site in BIBO3304. Arch Pharm (Weinheim). 2015 Jun;348(6):390-8. doi: 10.1002/ardp.201400427. Epub 2015 Apr 17. PubMed PMID: 25884646. 8: Forbes S, Herzog H, Cox HM. A role for neuropeptide Y in the gender-specific gastrointestinal, corticosterone and feeding responses to stress. Br J Pharmacol. 2012 Aug;166(8):2307-16. doi: 10.1111/j.1476-5381.2012.01939.x. PubMed PMID: 22404240; PubMed Central PMCID: PMC3448895. 9: Keller M, Kaske M, Holzammer T, Bernhardt G, Buschauer A. Dimeric argininamide-type neuropeptide Y receptor antagonists: chiral discrimination between Y1 and Y4 receptors. Bioorg Med Chem. 2013 Nov 1;21(21):6303-22. doi: 10.1016/j.bmc.2013.08.065. Epub 2013 Sep 8. PubMed PMID: 24074877. 10: Morales-Medina JC, Dumont Y, Benoit CE, Bastianetto S, Flores G, Fournier A, Quirion R. Role of neuropeptide Y Y₁ and Y₂ receptors on behavioral despair in a rat model of depression with co-morbid anxiety. Neuropharmacology. 2012 Jan;62(1):200-8. doi: 10.1016/j.neuropharm.2011.06.030. Epub 2011 Jul 23. PubMed PMID: 21803058. 11: Abdel-Samad D, Perreault C, Ahmarani L, Avedanian L, Bkaily G, Magder S, D'Orléans-Juste P, Jacques D. Differences in neuropeptide Y-induced secretion of endothelin-1 in left and right human endocardial endothelial cells. Neuropeptides. 2012 Dec;46(6):373-82. doi: 10.1016/j.npep.2012.09.003. Epub 2012 Oct 26. PubMed PMID: 23107364. 12: Cohen H, Liu T, Kozlovsky N, Kaplan Z, Zohar J, Mathé AA. The neuropeptide Y (NPY)-ergic system is associated with behavioral resilience to stress exposure in an animal model of post-traumatic stress disorder. Neuropsychopharmacology. 2012 Jan;37(2):350-63. doi: 10.1038/npp.2011.230. Epub 2011 Oct 5. PubMed PMID: 21976046; PubMed Central PMCID: PMC3242318. 13: Sapunar D, Vukojević K, Kostić S, Puljak L. Attenuation of pain-related behavior evoked by injury through blockade of neuropeptide Y Y2 receptor. Pain. 2011 May;152(5):1173-81. doi: 10.1016/j.pain.2011.01.045. Epub 2011 Mar 3. PubMed PMID: 21376464. 14: Capurro D, Huidobro-Toro JP. The involvement of neuropeptide Y Y1 receptors in the blood pressure baroreflex: studies with BIBP 3226 and BIBO 3304. Eur J Pharmacol. 1999 Jul 9;376(3):251-5. PubMed PMID: 10448884. 15: Fendt M, Bürki H, Imobersteg S, Lingenhöhl K, McAllister KH, Orain D, Uzunov DP, Chaperon F. Fear-reducing effects of intra-amygdala neuropeptide Y infusion in animal models of conditioned fear: an NPY Y1 receptor independent effect. Psychopharmacology (Berl). 2009 Oct;206(2):291-301. doi: 10.1007/s00213-009-1610-8. Epub 2009 Jul 17. PubMed PMID: 19609506. 16: Sousa DM, Baldock PA, Enriquez RF, Zhang L, Sainsbury A, Lamghari M, Herzog H. Neuropeptide Y Y1 receptor antagonism increases bone mass in mice. Bone. 2012 Jul;51(1):8-16. doi: 10.1016/j.bone.2012.03.020. Epub 2012 Mar 28. PubMed PMID: 22484690. 17: Solway B, Bose SC, Corder G, Donahue RR, Taylor BK. Tonic inhibition of chronic pain by neuropeptide Y. Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):7224-9. doi: 10.1073/pnas.1017719108. Epub 2011 Apr 11. PubMed PMID: 21482764; PubMed Central PMCID: PMC3084123. 18: Ito N, Hori A, Yabe T, Nagai T, Oikawa T, Yamada H, Hanawa T. Involvement of neuropeptide Y signaling in the antidepressant-like effect and hippocampal cell proliferation induced by kososan, a Kampo medicine, in the stress-induced depression-like model mice. Biol Pharm Bull. 2012;35(10):1775-83. PubMed PMID: 23037167. 19: Mahinda TB, Taylor BK. Intrathecal neuropeptide Y inhibits behavioral and cardiovascular responses to noxious inflammatory stimuli in awake rats. Physiol Behav. 2004 Feb;80(5):703-11. 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