( E )- N -(3-(5-(3-Acetamidopropyl)-3,6-dioxopiperazin-2-yl)propyl)-5-hydroxy-3-methylpent-2-enamide

: The Atacama Desert is an unexplored habitat with interesting possibilities for natural product chemistry due to the adaptations employed by microorganisms to survive the extreme salinity and high UV radiation present. Several soil samples were collected over the course of a few years in locations across the desert from which microorganisms were isolated. This paper reports on the isolation and structural characterisation, using LC-MS, and 1D and 2D NMR, of a new diketopiperazine that came from one of the fungi isolated from the Atacama Desert.


Introduction
Secondary metabolites in the form of scaffolds and pharmaceutically active compounds have been a rich source of novel chemistry for several decades, and perhaps even for a couple of centuries, starting with the isolation of morphine by Serturner from poppy seeds.These metabolites form the frontline drugs against a variety of diseases including cancer and bacterial and viral infections.Examples of such drugs include doxorubicin, an extremely potent anticancer drug produced by the bacterium Streptomyces peucetius [1]; lovastatin, which is a cholesterol-reducing drug isolated from Aspergillus terreus [2]; and the cephalosporin class of antibiotics isolated from the fungal genus Acremonium, which are known to act against a wide spectrum of bacterial infections.However, due to technical issues such as a high rate of rediscovery and the low availability of materials for clinical trials, their usage has dropped in the past few decades [3].Certain extreme environments such as the Atacama Desert in the north of Chile continue to attract the interest of natural product chemists from around the world due to its hostile elements, such as high salinity and UV radiation, which lead to interesting adaptations [4], and thus, secondary metabolites [5].Several interesting classes of potential therapeutics have been isolated from microorganisms found in the desert.These include lasso-peptides, chaxamycins, and aminoheptosyl glycosides [6], among other classes.This paper reports on the isolation and structural characterisation of albrnazine PS (1, see Figure 1), a new diketopiperazine from the fungal strain GP-3F-which was isolated from the Salar Tati region of the Atacama Desert.
The specific rotation, []  21 , was measured to be −331.4°.The FTIR spectrum, as seen in Figure 3(full report in Figure S7), of the compound in Based on the above spectroscopic analysis, the planar structure of 1 was established as depicted, representing a new 2,5-diketopiperazine for which we suggest the name albrnazine PS.Based on the above spectroscopic analysis, the planar structure of 1 was established as depicted, representing a new 2,5-diketopiperazine for which we suggest the name albrnazine PS.

Isolation and Cultivation of the Fungus
The fungus was isolated from a sample of soil collected at 23.00.010 S, 67.15.822W at an altitude of 4339 m, as described previously [7].The isolated fungus (strain # GP-3F) was submitted to NCIMB (Aberdeen, UK) for identification (GenBank accession #NC022575_GP-3F-), but did not give a sufficiently high species level match in the MicroSeq database.Therefore, the sequence was searched against the non-validated EMBL public database, with the top matches Chrysosporium merdarium and Geomyces pannorum var.pannorum each displaying a 99.65% similarity.The strain was stored on ISP2 plates at 4 • C and in 25% glycerol stock solutions at −80 • C. The fungus was cultivated in two 1 L Erlenmeyer flasks, each containing 100 g of rice and 100 mL of water, autoclaved at 121 • C for 20 min, and sealed off using cotton wool and aluminium foil at room temperature for 4 weeks.

Isolation and Structural Characterisation of Albrnazine PS (1)
After cultivation for 4 weeks, the fungal culture was extracted using 200 mL of methanol 3 times per flask, which was followed by using 200 mL of ethyl acetate 2 times per flask, after which the combined extracts were dried under vacuum.The dried extract was redissolved in methanol and subjected to flash chromatography using a Buchi Reveleris X2 flash chromatography system with a C-18 column (Flashpure eco-flex 80 g; particle size: 50 µm; pore size: 92-108 Å) for the stationary phase, whereas the mobile phase utilized a starting gradient of water and methanol, which yielded four fractions.The third fraction was subjected to semi-preparative HPLC using an Agilent 1100 series binary pump and 1100 series DAD (diode array detector) with a Sunfire column (10 µm, 10 mm × 250 mm) at 2 mL/min, resulting in 3.2 mg of albrnazine PS (1) being isolated.LC-MS was performed using an Agilent 1290 infinity UHPLC and a Phenomenex Kinetex XB-C18 (2.6 µM, 100 × 2.1 mm 2 ) column with mobile phases of 5% acetonitrile + 0.1% formic acid and 94.9% water, and 100% acetonitrile + 0.1% formic acid.MS spectra were obtained using a Bruker Maxis Q-tof II (Coventry, UK) where the mass range was set from 100-2000, the capillary voltage was set to 4.5 kV, the nebuliser gas was set to 4 bar, the dry gas was set to 9 L/min, and the dry temperature was set to 220 • C. The MS/MS experiments were conducted under Auto MS/MS scan mode with a step collision energy from 80 to 200%.A Bruker Avance III HD 400 MHz system (Coventry, UK) was used to acquire NMR spectra at 25 • C. The IR spectrum of the compound was measured using a Nicolet summit OA FTIR spectrometer, which was fitted with a DTGS-KBR detector at room temperature.

Conclusions
This paper reports the structural characterisation, using LC-MS, 1D and 2D NMR spectroscopy, of a new 2,5 diketopiperazine isolated from a fungus obtained from a soil sample from the Atacama Desert.The name albrnazine PS has been proposed for this compound.Author Contributions: Conceptualisation, G.P. and R.V.A.; methodology, G.P., J.E.R. and E.T.O.; software, G.P.; validation, R.E. and M.J.; formal analysis, G.P., R.E. and M.J.; investigation, G.P., R.E. and M.J.; resources, G.P.; data curation, G.P.; writing-original draft preparation, R.V.A.; writing-review and editing, G.P, R.E. and M.J.; visualisation, G.P. and R.V.A.; supervision, R.E. and M.J.; project administration, R.E. and M.J.; funding acquisition, M.J.All authors have read and agreed to the published version of the manuscript.

Supplementary Materials:
Funding: The collection of materials was carried out with financial support from the UK Newton Project for UK-Chile Collaboration (JIC CA 586) to Professor Mervyn Bibb, John Inness Centre, Norwich, UK.

Data Availability Statement:
The spectroscopic data presented in this study are available as Supplementary Materials.
−1 , signifying the solvent and perhaps occluding the −OH, −NH (secondary amine), and −CH (alkene) stretching modes.A strong peak at 1660 cm −1 indicates the C=O stretching mode of the amide groups and C=C stretching of the triply substituted alkene.Another strong peak at 1023 cm −1 indicates the C−O stretching mode of the primary alcohol at position 12.

Figure 2 .
Figure 2. Key COSY (bold), HMBC, and NOE correlations (arrows, from H-to C) for albrnanazine PS.The HMBC spectrum (see Figure 2 and Figure S5) displayed key correlations between H-3 and C-1', C-4, and C-5; H 2 -6 and C-8; NH-7 and C-8; H-9 and C-8, C-10, C-11, and C-13; H 2 -11 and C-9, C-10, C-12, and C-13; and H 3 -13 and C-9, C-10, and C-11.The stereochemistry of the double bond was established as E based on 2D NOE data (Figure S6) which displayed a strong through-space correlation between protons H-9 and H 2 -11.The specific rotation, [α] 21 D , was measured to be −331.4• .The FTIR spectrum, as seen in Figure 3 (full report in Figure S7), of the compound in methanol revealed a broad peak between 3600 and cm −1 , signifying the solvent and perhaps occluding the −OH, −NH (secondary amine), and −CH (alkene) stretching modes.A strong peak at 1660 cm −1 indicates the C=O stretching mode of the amide groups and C=C stretching of the triply substituted alkene.Another strong peak at 1023 cm −1 indicates the C−O stretching mode of the primary alcohol at position 12.

a δC (ppm) δH (ppm), Multiplicity (J in Hz) COSY a HMBC a
a Overlapping signals related by pseudosymmetry that are separated by "/".
a Overlapping signals related by pseudosymmetry that are separated by "/".