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432:; Sheldrick, W. S. (1993). "Pigments of fungi. 62. Haematopodin, an unusual pyrrologuinone derivative isolated from the fungus
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InChI=1S/C13H12N2O3/c16-9-5-8-11-7(6-14-12(11)13(9)17)4-10-15(8)2-1-3-18-10/h5-6,10,14H,1-4H2/t10-/m1/s1
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Hopmann, C.; Steglish, W. (1996). "Synthesis of haematopodin – A pigment from the mushroom
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for haematopodin was reported in 1996. Key steps in the synthesis involved the
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Except where otherwise noted, data are given for materials in their
376:(with the 1,3,4,5-tetrahydropyrroloquinoline structure), known as
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368:, although haematopodin only occurs in trace amounts in fresh
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438:Angewandte Chemie International Edition in English
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396:of 3--1-propanol to the indolo-6,7-quinone and
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428:Baumann, C.; Bröckelmann, M.; Fugmann, B.;
362:. Both compounds are found in the mushroom
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358:is the more stable breakdown product of
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229:Key: GTVMGUBGOSWMOJ-SNVBAGLBSA-N
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588:Heterocyclic compounds with 4 rings
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317:(at 25 °C , 100 kPa).
250:O=C3/C=C2/N4CCCO4Cc1cc(c12)C3=O
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53:-oxazolopyrroloquinoline-2,3(4
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511:. You can help Knowledge by
603:Heterocyclic compound stubs
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481:10.1002/jlac.199619960709
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563:Alkaloids found in fungi
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450:10.1002/anie.199310871
598:Tetracyclic compounds
578:Nitrogen heterocycles
505:heterocyclic compound
503:This article about a
384:, have been found in
406:trifluoroacetic acid
37:Preferred IUPAC name
583:Oxygen heterocycles
568:Biological pigments
558:Quinoline alkaloids
467:(Basidiomycetes)".
307: g·mol
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390:chemical synthesis
344:Infobox references
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465:Mycena haematopus
434:Mycena haematopus
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365:Mycena haematopus
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475:(7): 1117–20.
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360:Haematopodin B
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370:fruit bodies
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64:Identifiers
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398:cyclization
386:sea sponges
259:Properties
81:151964-21-5
552:Categories
412:References
378:batzellins
372:. Similar
300:Molar mass
170:838N74Y28P
116:ChemSpider
92:3D model (
71:CAS Number
382:damirones
573:Quinones
394:addition
374:pigments
150:10857709
125:10473906
337:what is
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305:244.250
137:PubChem
57:)-dione
593:Enones
402:adduct
332:verify
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243:SMILES
31:Names
507:is a
404:with
388:. A
218:InChI
94:JSmol
509:stub
473:1996
380:and
161:UNII
477:doi
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187:EPA
140:CID
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327:Y
293:3
290:O
287:2
284:N
278:H
272:C
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185:(
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55:H
51:H
47:H
43:R
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