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1 Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2017 Supporting Information Synthesis and Biological Evaluation of the Ascidian Blood-Pigment Halocyamine A Hugo K. H. Fong, a Jean Michel Brunel, b Arlette Longeon, c Marie-Lise Bourguet-Kondracki, c David Barker, a and Brent R. Copp* a a School of Chemical Sciences, University of Auckland, 23 Symonds St, Auckland 1010, New Zealand b Centre de Recherche en Cancérologie de Marseille (CRCM), CNRS, UMR7258, Institut Paoli Calmettes, Aix- Marseille Université, UM 105, Inserm, U1068, F Marseille, France c Laboratoire Molécules de Communication et Adaptation des Micro-organismes, UMR 7245 CNRS, Muséum National d Histoire Naturelle, 57 rue Cuvier (C.P. 54), Paris, France. * Corresponding author b.copp@auckland.ac.nz Contents: Table S1. NMR data of isolated halocyamine A (1) and synthetic halocyamine A HCl salt (1)...S2 1 H and 13 C NMR Spectra..S3 S44 S1
2 Table S1. NMR data of isolated halocyamine A (1) and synthetic halocyamine A HCl salt (1) in DMSO-d6. Atom 1 H [δ, mult., J (Hz)] 13 C (δ) No. Isolated (1) 1 Synthetic (1) Isolated (1) 1 Synthetic (1) 1 Not observed Not observed (8.37 [3H, br s]) * (1H, t, 5.0) 3.61 (1H, br s) (1H, dd, 15.5, 5.0), (1H, m), 2.93 (1H, dd, 15.5, 7.5) 2.73 (1H, dd, 14.3, 7.5) (1H, s) 7.60 (1H, s) Not observed Not observed (1H, s) 6.86 (1H, s) Not observed (118.2) * (1H, br d, 6.8) 8.40 (1H, br s) (1H, m) 4.44 (1H, br s) #, 2.95 (1H, dd, 14.0, 4.1), 2.65 (1H, dd, 14.0, 10.5), 2.66 (1H, dd, 14.0, 9.6) (1H, d, 1.8) 6.64 (1H, d, 1.5) (1H, d, 8.0) 6.59 (1H, d, 8.0) (1H, dd, 8.0, 1.8) 6.45 (1H, dd, 8.0, 1.5) (1H, br t, 6.5) 8.88 (1H, br s) (2H, d, 5.5) 3.99 (1H, dd, 16.6, 5.8), 3.93 (1H, dd, 16.6, 5.8) (1H, d, 10.5) 9.08 (1H, d, 10.0) (1H, t, 9.5) 6.67 (1H, dd, 10.0, 9.7) (1H, d, 9.5) 5.92 (1H, d, 9.7) (1H, s) 7.72 (1H, s) (1H, s) (1H, br s) a (1H, d, 2.0) 7.58 (1H, d, 1.6) (1H, dd, 8.5, 2.0) 7.16 (1H, dd, 8.3, 1.6) (1H, d, 8.5) 7.56 (1H, d, 8.3) a *signals observed for synthetic halocyamine A TFA salt in DMSO-d6. # 3.00 ppm, dd, J = 14.0 and 5.6 Hz, in CH3OD Reference (1) K. Azumi, H. Yokosawa, S. Ishii, Biochemistry 1990, 29, S2
3 1 H NMR (CDCl3, 500 MHz) of Fmoc-His(Trt)-DOPA(TBDMS)2-Gly-OH (4). S3
4 13 C NMR (CDCl3, 125 MHz) of Fmoc-His(Trt)-DOPA(TBDMS)2-Gly-OH (4). S4
5 1 H NMR (CDCl3, 500 MHz) of Fmoc-His(Trt)-DOPA(TBDMS)2-Gly-NH2 (3). S5
6 13 C NMR (CDCl3, 125 MHz) of Fmoc-His(Trt)-DOPA(TBDMS)2-Gly-NH2 (3). S6
7 1 H NMR (CDCl3, 500 MHz) of a mixture of (Z)-but-1-en-3-yne-1,4-diyldibenzene (5) and (E)-but-1-en-3-yne-1,4-diyldibeneze (6). S7
8 13 C NMR (CDCl3, 125 MHz) of a mixture of (Z)-but-1-en-3-yne-1,4-diyldibenzene (5) and (E)-but-1-en-3-yne-1,4-diyldibeneze (6). S8
9 1 H NMR (CDCl3, 500 MHz) of (Z)-(9H-fluoren-9-yl)methyl (2-oxo-2-(styrylamino)ethyl)carbamate (10). S9
10 13 C NMR (CDCl3, 125 MHz) of (Z)-(9H-fluoren-9-yl)methyl (2-oxo-2-(styrylamino)ethyl)carbamate (10). S10
11 1 H NMR (CDCl3, 400 MHz) of tert-butyl (Z)-(2-oxo-2-(styrylamino)ethyl)carbamate (12). S11
12 13 C NMR (CDCl3, 100 MHz) of tert-butyl (Z)-(2-oxo-2-(styrylamino)ethyl)carbamate (12). S12
13 1 H NMR (CDCl3, 500 MHz) of (Z)-2-amino-N-styrylacetamide (8). S13
14 13 C NMR (CDCl3, 125 MHz) of (Z)-2-amino-N-styrylacetamide (8). S14
15 1 H NMR (CDCl3, 500 MHz) of Fmoc-His(Trt)-DOPA(TBDMS)2-OH (7). S15
16 13 C NMR (CDCl3, 125 MHz) of Fmoc-His(Trt)-DOPA(TBDMS)2-OH (7). S16
17 1 H NMR (CDCl3, 500 MHz) of (9H-fluoren-9-yl)methyl ((S)-1-(((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-oxo-1-((2-oxo-2-(((Z)- styryl)amino)ethyl)amino)propan-2-yl)amino)-1-oxo-3-(1-trityl-1h-imidazol-4-yl)propan-2-yl)carbamate (13). S17
18 13 C NMR (CDCl3, 125 MHz) of (9H-fluoren-9-yl)methyl ((S)-1-(((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-oxo-1-((2-oxo-2-(((Z)- styryl)amino)ethyl)amino)propan-2-yl)amino)-1-oxo-3-(1-trityl-1h-imidazol-4-yl)propan-2-yl)carbamate (13). S18
19 1 H NMR (CDCl3, 400 MHz) of (S)-2-amino-N-((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-oxo-1-((2-oxo-2-(((Z)- styryl)amino)ethyl)amino)propan-2-yl)-3-(1-trityl-1h-imidazol-4-yl)propanamide (14). S19
20 13 C NMR (CDCl3, 125 MHz) of (S)-2-amino-N-((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-oxo-1-((2-oxo-2-(((Z)- styryl)amino)ethyl)amino)propan-2-yl)-3-(1-trityl-1h-imidazol-4-yl)propanamide (14). S20
21 1 H NMR (CD3OD, 500 MHz) of (S)-2-amino-N-((S)-3-(3,4-dihydroxyphenyl)-1-oxo-1-((2-oxo-2-(((Z)-styryl)amino)ethyl)amino)propan-2-yl)- 3-(1-trityl-1H-imidazol-4-yl)propanamide (15). S21
22 13 C NMR (CD3OD, 125 MHz) of (S)-2-amino-N-((S)-3-(3,4-dihydroxyphenyl)-1-oxo-1-((2-oxo-2-(((Z)-styryl)amino)ethyl)amino)propan-2-yl)- 3-(1-trityl-1H-imidazol-4-yl)propanamide (15). S22
23 1 H NMR (DMSO-d6, 500 MHz) of 4-((S)-2-ammonio-3-(((S)-3-(3,4-dihydroxyphenyl)-1-oxo-1-((2-oxo-2-(((Z)- styryl)amino)ethyl)amino)propan-2-yl)amino)-3-oxopropyl)-1h-imidazol-3-ium chloride (2). S23
24 13 C NMR (DMSO-d6, 125 MHz) of 4-((S)-2-ammonio-3-(((S)-3-(3,4-dihydroxyphenyl)-1-oxo-1-((2-oxo-2-(((Z)- styryl)amino)ethyl)amino)propan-2-yl)amino)-3-oxopropyl)-1h-imidazol-3-ium chloride (2). S24
25 1 H NMR (CDCl3, 400 MHz) of tert-butyl-6-bromo-3-iodo-1h-indole-1-carboxylate (19). S25
26 1 H NMR (CDCl3, 400 MHz) of tert-butyl-6-bromo-3-iodo-1h-indole-1-carboxylate (19) S26
27 1 H NMR (CDCl3, 400 MHz) of tert-butyl 6-bromo-3-((trimethylsilyl)ethynyl)-1H-indole-1-carboxylate (20). S27
28 13 C NMR (CDCl3, 100 MHz) of tert-butyl 6-bromo-3-((trimethylsilyl)ethynyl)-1H-indole-1-carboxylate (20). S28
29 1 H NMR (CDCl3, 400 MHz) of tert-butyl 6-bromo-3-ethynyl-1H-indole-1-carboxylate (17). S29
30 13 C NMR (CDCl3, 100 MHz) of tert-butyl 6-bromo-3-ethynyl-1H-indole-1-carboxylate (17). S30
31 1 H NMR (CDCl3, 400 MHz) of tert-butyl (Z)-3-(2-(2-aminoacetamido)vinyl)-6-bromo-1H-indole-1-carboxylate (21). S31
32 13 C NMR (CDCl3, 100 MHz) of tert-butyl (Z)-3-(2-(2-aminoacetamido)vinyl)-6-bromo-1H-indole-1-carboxylate (21). S32
33 1 H NMR (CDCl3, 400 MHz) of (E)-di-tert-butyl 3,3'-(but-1-en-3-yne-1,4-diyl)bis(6-bromo-1H-indole-1-carboxylate) (22). S33
34 13 C NMR (CDCl3, 100 MHz) of (E)-di-tert-butyl 3,3'-(but-1-en-3-yne-1,4-diyl)bis(6-bromo-1H-indole-1-carboxylate) (22). S34
35 1 H NMR (DMSO-d6, 400 MHz) of (Z)-2-amino-N-(2-(6-bromo-1H-indol-3-yl)vinyl)acetamide (16). S35
36 13 C NMR (DMSO-d6, 100 MHz) of (Z)-2-amino-N-(2-(6-bromo-1H-indol-3-yl)vinyl)acetamide (16). S36
37 1 H NMR (CDCl3, 500 MHz) of (9H-fluoren-9-yl)methyl ((S)-1-(((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-((2-(((Z)-2-(6-bromo-1Hindol-3-yl)vinyl)amino)-2-oxoethyl)amino)-1-oxopropan-2-yl)amino)-1-oxo-3-(1-trityl-1H-imidazol-4-yl)propan-2-yl)carbamate (23). S37
38 13 C NMR (CDCl3, 125 MHz) of (9H-fluoren-9-yl)methyl ((S)-1-(((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-((2-(((Z)-2-(6-bromo- 1H-indol-3-yl)vinyl)amino)-2-oxoethyl)amino)-1-oxopropan-2-yl)amino)-1-oxo-3-(1-trityl-1H-imidazol-4-yl)propan-2-yl)carbamate (23). S38
39 1 H NMR (CDCl3, 500 MHz) of (S)-2-amino-N-((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-((2-(((Z)-2-(6-bromo-1H-indol-3- yl)vinyl)amino)-2-oxoethyl)amino)-1-oxopropan-2-yl)-3-(1-trityl-1h-imidazol-4-yl)propanamide (24). S39
40 13 C NMR (CDCl3, 125 MHz) of (S)-2-amino-N-((S)-3-(3,4-bis((tert-butyldimethylsilyl)oxy)phenyl)-1-((2-(((Z)-2-(6-bromo-1H-indol-3- yl)vinyl)amino)-2-oxoethyl)amino)-1-oxopropan-2-yl)-3-(1-trityl-1h-imidazol-4-yl)propanamide (24). S40
41 1 H NMR (CD3OD, 500 MHz) of (S)-2-amino-N-((S)-1-((2-(((Z)-2-(6-bromo-1H-indol-3-yl)vinyl)amino)-2-oxoethyl)amino)-3-(3,4- dihydroxyphenyl)-1-oxopropan-2-yl)-3-(1-trityl-1h-imidazol-4-yl)propanamide (25). S41
42 13 C NMR (CD3OD, 125 MHz) of (S)-2-amino-N-((S)-1-((2-(((Z)-2-(6-bromo-1H-indol-3-yl)vinyl)amino)-2-oxoethyl)amino)-3-(3,4- dihydroxyphenyl)-1-oxopropan-2-yl)-3-(1-trityl-1h-imidazol-4-yl)propanamide (25). S42
43 1 H NMR (DMSO-d6, 500 MHz) of halocyamine A dihydrochloride salt (1). S43
44 13 C NMR (DMSO-d6, 125 MHz) of halocyamine A dihydrochloride salt (1). S44
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