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MedKoo Cat#: 462140 | Name: Fellutanine A
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Description:

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

Fellutanine A is a diketopiperazine fungal metabolite that has been found in A. candidus.

Chemical Structure

Fellutanine A
Fellutanine A
CAS#175414-35-4

Theoretical Analysis

MedKoo Cat#: 462140

Name: Fellutanine A

CAS#: 175414-35-4

Chemical Formula: C22H20N4O2

Exact Mass: 372.1586

Molecular Weight: 372.43

Elemental Analysis: C, 70.95; H, 5.41; N, 15.04; O, 8.59

Price and Availability

Size Price Availability Quantity
1mg USD 450.00 2 Weeks
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Related CAS #
No Data
Synonym
Fellutanine A; fellutanine; cyclo(Trp-Trp); cyclo-(L-Trp-D-Trp)
IUPAC/Chemical Name
(3R,6S)-3,6-bis(1H-indol-3-ylmethyl)-2,5-piperazinedione
InChi Key
DNHODRZUCGXYKU-BGYRXZFFSA-N
InChi Code
InChI=1S/C22H20N4O2/c27-21-19(9-13-11-23-17-7-3-1-5-15(13)17)25-22(28)20(26-21)10-14-12-24-18-8-4-2-6-16(14)18/h1-8,11-12,19-20,23-24H,9-10H2,(H,25,28)(H,26,27)/t19-,20+
SMILES Code
O=C(N[C@@H](CC1=CNC2=CC=CC=C21)C(N3)=O)[C@H]3CC4=CNC5=CC=CC=C54
Appearance
Solid powder
Purity
>70% (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
>3 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 372.43 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
1: Shan T, Wang Y, Wang S, Xie Y, Cui Z, Wu C, Sun J, Wang J, Mao Z. A new p-terphenyl derivative from the insect-derived fungus Aspergillus candidus Bdf-2 and the synergistic effects of terphenyllin. PeerJ. 2020 Jan 2;8:e8221. doi: 10.7717/peerj.8221. PMID: 31915570; PMCID: PMC6942676. 2: May Zin WW, Buttachon S, Dethoup T, Fernandes C, Cravo S, Pinto MM, Gales L, Pereira JA, Silva AM, Sekeroglu N, Kijjoa A. New Cyclotetrapeptides and a New Diketopiperzine Derivative from the Marine Sponge-Associated Fungus Neosartorya glabra KUFA 0702. Mar Drugs. 2016 Jul 20;14(7):136. doi: 10.3390/md14070136. PMID: 27447650; PMCID: PMC4962026. 3: Kumla D, Shine Aung T, Buttachon S, Dethoup T, Gales L, Pereira JA, Inácio Â, Costa PM, Lee M, Sekeroglu N, Silva AMS, Pinto MMM, Kijjoa A. A New Dihydrochromone Dimer and Other Secondary Metabolites from Cultures of the Marine Sponge-Associated Fungi Neosartorya fennelliae KUFA 0811 and Neosartorya tsunodae KUFC 9213. Mar Drugs. 2017 Dec 1;15(12):375. doi: 10.3390/md15120375. PMID: 29194412; PMCID: PMC5742835. 4: Ezekiel CN, Kraak B, Sandoval-Denis M, Sulyok M, Oyedele OA, Ayeni KI, Makinde OM, Akinyemi OM, Krska R, Crous PW, Houbraken J. Diversity and toxigenicity of fungi and description of Fusarium madaense sp. nov. from cereals, legumes and soils in north-central Nigeria. MycoKeys. 2020 Jun 8;67:95-124. doi: 10.3897/mycokeys.67.52716. PMID: 32565683; PMCID: PMC7295817. 5: Schulz D, Ohlendorf B, Zinecker H, Schmaljohann R, Imhoff JF. Eutypoids B-E produced by a Penicillium sp. strain from the North Sea. J Nat Prod. 2011 Jan 28;74(1):99-101. doi: 10.1021/np100633k. Epub 2010 Dec 3. PMID: 21126094. 6: de Carvalho AC, Lima CS, Torquato HFV, Domiciano AT, Silva SDC, de Abreu LM, Uemi M, Paredes-Gamero EJ, Vieira PC, Veiga TAM, de Medeiros LS. Chemodiversity and Anti-Leukemia Effect of Metabolites from Penicillium setosum CMLD 18. Metabolites. 2022 Dec 23;13(1):23. doi: 10.3390/metabo13010023. PMID: 36676948; PMCID: PMC9864219. 7: Singla R, Jaitak V. Multitargeted Molecular Docking Study of Natural-Derived Alkaloids on Breast Cancer Pathway Components. Curr Comput Aided Drug Des. 2017 Nov 10;13(4):294-302. doi: 10.2174/1573409913666170406144642. PMID: 28382865. 8: Vinokurova NG, Boĭchenko LV, Arinbasarov MU. Obrazovanie alkaloidov gribami roda Penicillium pri roste na zerne pshenitsy [Formation of alkaloids from Penicillium species fungi during growth on wheat kernels]. Prikl Biokhim Mikrobiol. 2003 Jul-Aug;39(4):457-60. Russian. PMID: 14520967. 9: Kozlovskiĭ AG, Vinokurova NG, Adanin VM. Diketodipiperazinovye alkaloidy gribov Penicillium piscarium Westling [Diketopiperazine alkaloids from the fungus Penicillium piscarium Westling]. Prikl Biokhim Mikrobiol. 2000 May- Jun;36(3):317-21. Russian. PMID: 10867952.