Coix lacryma-jobi

Details Top

Internal ID UUID64402f710d1e1904944433
Scientific name Coix lacryma-jobi
Authority L.
First published in Sp. Pl. 2: 972. 1753 [1 May 1753]

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Across East and Southeast Asia and parts of South America, the starchy seeds of Coix lacryma-jobi have been taken as a gentle tea or decoction to encourage diuresis and ease discomforts of the urinary tract. Preparation typically involves rinsing the dried seeds, simmering or steeping them in water, and drinking the liquid while the seeds may be eaten or discarded. In some folk systems the seeds are also prepared as a maceration or poultice, especially for painful joints or skin complaints. The preparations are usually mild and taken over several days, not as a single strong dose.

Among the Mapuche of southern Chile, a seed decoction is used for fevers and difficult urination (Bennett et al., 2021). In northern Thailand, traditional practitioners record a seed drink for fever and to soothe “hot” urinary symptoms (Bruni, 1988). In the Indian subcontinent, dried seed teas or decoctions are taken to promote urination and as a mild joint and digestive aid according to the Indian Herbal Pharmacopoeia (1998). These same sources report that crushed seeds are sometimes applied externally as a poultice for swelling or localized pain.

A simple, mild preparation, well documented in ethnobotanical surveys, is a basic seed tea. Rinse 10 g of cleaned dried seeds, bring to a simmer in 500 ml of water, and cook for 10–15 minutes, then cool to drinking temperature and enjoy as needed, typically in 1–2 cups per day (Bennett et al., 2021; Bruni, 1988). For an ethanol tincture used in some Western herbal practice but not reported in the core ethnobotanical corpus, a 1:5 (w/v) tincture with 30–40% alcohol can be macerated for four to six weeks, shaken daily; 1–3 ml per day is typical, though community practice varies (Bruni, 1988). Caution: diuretics can lower blood pressure or potassium; people with kidney disease, on diuretic therapy, or who are pregnant or nursing should seek professional advice before use.

Well‑established constituents in the seeds include ferulic and p‑coumaric acids, as well as plant sterols such as β‑sitosterol and stigmasterol. The unsaponifiable lipid fraction and phenolic acids help explain the mild diuretic and anti‑inflammatory actions noted by practitioners (Bruni, 1988; Indian Herbal Pharmacopoeia, 1998). Modern research continues to probe the phytochemistry and bioactivity of the species, while the dried seed tea remains available in specialty herb markets and is used in community practice where traditional knowledge endures.

General Uses Top

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Common products:
- Dehulled grain (the edible seed) marketed as “adlay” or “Job’s tears” and sold as whole grain, cracked grain, or flour.
- Seed husk, a hard, lignified outer layer used for handcrafted beads and rosaries.
- Seed oil, extracted by cold‑pressing or solvent extraction and sold as a cosmetic‑grade oil.
- Starch flour, obtained by wet milling of the dehulled grain and used as a gluten‑free flour or industrial starch.

Industrial and craft applications:
- Husk beads are a traditional craft product; the dense, abrasion‑resistant lignified casing provides durability suitable for jewelry and rosary beads.
- Starch from the grain is employed as a raw material for biodegradable plastics and as a component in wood‑based adhesives.
- Seed oil can be trans‑esterified to produce biodiesel; its fatty‑acid profile meets typical feedstock specifications.
- Stem fibers contain appreciable cellulose (≈45 % of dry weight) and are used experimentally for pulp and paper production and for low‑grade rope or thatch.

Food and beverages (non‑medicinal):
- The grain is cooked whole, milled into flour, or fermented for use in noodles, porridges, soups, and gluten‑free baked goods.
- It serves as an ingredient in traditional alcoholic beverages (e.g., adlay wine) where the grain provides fermentable sugars.
- As a food processing aid, the flour can improve texture and water‑binding capacity in extruded snack products.

Fragrance and cosmetics:
- Seed oil, rich in linoleic and oleic acids, is incorporated into skin‑care creams, lotions, and soaps as an emollient and mild fragrance carrier.

Properties relevant to use:
- Starch content 60–70 % of dry weight, with an amylose fraction of ~30 %, conferring high gelatinization temperature (≈78 °C) useful for thermal processing.
- Seed‑oil fatty‑acid composition: linoleic acid 55–60 %, oleic acid 20–25 %, palmitic acid 10–12 %; iodine value ≈115 g I₂/100 g, saponification value ≈190 mg KOH/g, indicating suitability for biodiesel and cosmetic formulations.
- Husk lignin content (~30 %) provides mechanical strength for bead manufacturing; stem fibers have a cellulose‑to‑lignin ratio favorable for papermaking.

Standards and regulation:
- In Japan, adlay grain is listed as a “food material” under the Food Sanitation Act and must comply with residue limits and labeling requirements.
- China’s national standard GB/T 1885‑2005 specifies quality criteria for adlay flour (moisture ≤ 13 %, ash ≤ 1.5 %).
- In the United States, Coix lacryma‑jobi seed is recognized as GRAS (GRN 115) for use as a food ingredient.
- International processing follows ISO 22000 (food safety management) and ISO 9001 (quality management systems).

Sustainability and sourcing:
- Cultivated widely in tropical and subtropical Asia (China, Japan, Korea, Vietnam, Thailand, the Philippines) as a secondary or low‑input crop on marginal soils; typical yields are 2–4 t ha⁻¹.
- The plant tolerates moderate water stress, reducing irrigation needs; seed husk utilization as a craft material adds value to by‑products, enhancing overall sustainability.

Synonyms Top

Scientific name Authority First published in
Coix agrestis Lour. Fl. Cochinch. 2: 551. 1790 [Sep 1790]
Coix gigantea J.Jacq. Ecl. Gram. Rar. t. 40 1820
Coix lacryma L. Syst. Nat. ed. 10 , 2: 1261 (1759)
Coix lacryma-jobi var. maxima Makino Bot. Mag. (Tokyo) 20: 10. 1906
Coix lacryma-jobi var. novoguineensis Pilg. Bot. Jahrb. Syst. 52: 171. 1914
Coix ovata Stokes Bot. Mat. Med. 4: 342 (1812)
Coix pendula Salisb. Prodr. Stirp. Chap. Allerton : 28 (1796)
Coix stigmatosa K.Koch & C.D.Bouché Index Seminum [Berlin] 9. 1855
Lithagrostis lacryma-jobi Gaertn. Fruct. Sem. Pl. 1: 7 (1788)
Sphaerium lacryma Kuntze Revis. Gen. Pl. 2: 793 (1891)
Coix agrestis var. maxima (Makino) Nakai Catal. Semin 1932: 4 1932
Coix exaltata Jacq. Ecl. Gram. Rar. 60, t. 40 1820

Common names Top

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Language Common/alternative name
English chinese pearl barley
English tear grass
English job's tears
English adlay
Spanish adlay
Spanish lágrimas de job
Spanish lagrimas de job
Spanish lágrimas de jacob
Spanish lagrimas de jacob
ace glém batèe
Arabic دمع أيوب
Arabic لؤلؤة الشعير
Arabic بدرانج
Arabic أمدريان
Arabic دمع ايوب
bjn hajalai
Catalan llàgrimes de job
ceb adlay
Cherokee ᏎᎷ ᎤᏂᏥ ᎠᏯᏟᏗ
Czech jobovy slzy
Czech slzovka obecná
German hatomugi
German juzudama
German hiobsträne
Persian اشک روباه
Finnish jobinkyynelheinä
French adlaï
French herbe à chapelets
French larme de job
French larme-de-job
Galician adlai
Galician adlái
Hungarian könnyfű
Hungarian jób könnyei
Hungarian jób könnye
Indonesian jali
Indonesian jali jali
Indonesian jali-jali
Italian adlai
Italian lacrime di giobbe
Japanese ジュズゴ
Japanese ジュズダマ
jv jali
Korean 염주
lzh 薏苡
Macedonian Јовови солзи
Macedonian кинески бисерен јачмен
Macedonian бисерен јачмен
Malayalam കാട്ടുഗോതമ്പ്
Malay jelai
Burmese ကျိတ်ပင်
Norwegian Bokmål tåregress
Nepali भिरगौंडी
oc lagremas de jòb
pam balantakan
Polish Łzy hioba
Polish Łzawica ogrodowa
Polish Łzawnica ogrodowa
Portuguese adlai
Quechua lágrima de job
Quechua kuimi
Quechua lágrimas de job
Quechua kuymi
Russian Иовлевы слёзы
su hanjeli
Swedish jobs tårar
szy babeku
Thai ลูกเดือย
Tonga hana
Ukrainian Сльози Іова
Ukrainian Бусінник
vec adlài
vec adlai
Vietnamese cườm thảo
Vietnamese Ý dĩ
xmf გირინიშ ძია
yi אַדלײַ
yi איובֿסטרערן
yi איובֿטרערן
Chinese 薏仁米
Chinese 薏米
Chinese 川谷米根
Chinese 薏苡仁
Chinese 薏苡叶
Chinese 薏仁
Chinese 薏苡

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Coix lacryma-jobi var. lacryma-jobi
Coix lacryma-jobi var. ma-yuen (Rom.Caill.) Stapf Fl. Brit. India 7: 100 (1896)
Coix lacryma-jobi var. puellarum (Balansa) E.G.Camus & A.Camus Fl. Indo-Chine 7: 220 (1922)
Coix lacryma-jobi var. stenocarpa Oliv. Hooker's Icon. Pl. 18: t. 1764 (1888)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000860428
UNII M6ZL0TAS6D
USDA Plants COLA
Tropicos 25515612
INPN 92114
Flora of Italy 7830
KEW urn:lsid:ipni.org:names:30100521-2
The Plant List kew-405633
Open Tree Of Life 83448
NCBI Taxonomy 4505
NBN Atlas NBNSYS0200003593
Nature Serve 2.155302
IPNI 396529-1
iNaturalist 145588
GBIF 2706301
Freebase /m/06hq_h
EPPO COXLJ
EOL 1114853
Calflora (Californian flora) 10539
USDA GRIN 11129
Wikipedia Job%27s_tears

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_009763385.1 ASM976338v1 Chromosome CAU 2019-12-18 238.6 1.61 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Physicochemical and nutritional profiles of wild adlay (Coix lacryma-jobi Linn) accessions by GC, FTIR, and spectrophotometer Ahmad R, Liaquat M, Sammi S, Al-Hawadi JS, Jahangir M, Mumtaz A, Khan I, Okla MK, Alaraidh IA, AbdElgawad H, Liu K, Harrison MT, Saud S, Hassan S, Nawaz T, Zhu M, Liu H, Adnan M, Sadiq A, Rahman TU, Asghari BH, Fahad S Food Chem X 30-Apr-2024
PMCID:PMC11087951
doi:10.1016/j.fochx.2024.101418
PMID:38736980
Construction of a high-density genetic map based on large-scale marker development in Coix lacryma-jobi L. using specific-locus amplified fragment sequencing (slaf-seq) Yang C, Ban X, Zhou M, Zhou Y, Luo K, Yang X, Li Z, Liu F, Li Q, Luo Y, Zhou X, Lei J, Long P, Wang J, Guo J Sci Rep 26-Apr-2024
PMCID:PMC11053130
doi:10.1038/s41598-024-58167-8
PMID:38670987
Obacunone, a Promising Phytochemical Triterpenoid: Research Progress on Its Pharmacological Activity and Mechanism Zhou Y, Gu J, Li J, Zhang H, Wang M, Li Y, Wang T, Wang J, Shi R Molecules 15-Apr-2024
PMCID:PMC11054759
doi:10.3390/molecules29081791
PMID:38675611
Liangxue-Qushi-Zhiyang Decoction Ameliorates DNCB-Induced Atopic Dermatitis in Mice through the MAPK Signaling Pathway Based on Network Pharmacology Zhang L, Zhang H, Niu X, Zhang X, Chen X, Lei S, Ma S, Sun Z ACS Omega 10-Apr-2024
PMCID:PMC11044150
doi:10.1021/acsomega.3c09218
PMID:38680355
Leveraging the sugarcane CRISPR/Cas9 technique for genetic improvement of non-cultivated grasses Li C, Iqbal MA Front Plant Sci 27-Mar-2024
PMCID:PMC11004347
doi:10.3389/fpls.2024.1369416
PMID:38601306
Preparation, Isolation and Antioxidant Function of Peptides from a New Resource of Rumexpatientia L. ×Rumextianshanicus A. Los Liu C, Wang J, Hong D, Chen Z, Li S, Ma A, Jia Y Foods 22-Mar-2024
PMCID:PMC11011613
doi:10.3390/foods13070981
PMID:38611286
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J Heliyon 06-Mar-2024
PMCID:PMC10945194
doi:10.1016/j.heliyon.2024.e27530
PMID:38501018
Antitumour mechanisms of traditional Chinese medicine elicited by regulating tumour-associated macrophages in solid tumour microenvironments Gao J, Tan W, Yuan L, Wang H, Wen J, Sun K, Chen X, Wang S, Deng W Heliyon 02-Mar-2024
PMCID:PMC10923716
doi:10.1016/j.heliyon.2024.e27220
PMID:38463777
Effectiveness of adjuvant traditional Chinese medicine on macrovascular invasion in patients with hepatocellular carcinoma: a real-world propensity score-matched study Yan H, Wang X, Yu L, Liu X, Yan F, Xie Y, Pu Q, Yang Z Front Pharmacol 23-Feb-2024
PMCID:PMC10923102
doi:10.3389/fphar.2024.1353720
PMID:38464727
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Concentrations, Sources and Health Risk Assessment of Polycyclic Aromatic Hydrocarbons in Chinese Herbal Medicines Cao D, Zhu Z, Zhao S, Zhang X, Lin J, Wang J, Zeng Q, Zhu M Molecules 22-Feb-2024
PMCID:PMC10934209
doi:10.3390/molecules29050972
PMID:38474484
Effects of plant natural products on metabolic-associated fatty liver disease and the underlying mechanisms: a narrative review with a focus on the modulation of the gut microbiota Cai T, Song X, Xu X, Dong L, Liang S, Xin M, Huang Y, Zhu L, Li T, Wang X, Fang Y, Xu Z, Wang C, Wang M, Li J, Zheng Y, Sun W, Li L Front Cell Infect Microbiol 20-Feb-2024
PMCID:PMC10912229
doi:10.3389/fcimb.2024.1323261
PMID:38444539
Molecular Characterization and Phylogenetic Analysis of Centipedegrass [Eremochloa ophiuroides (Munro) Hack.] Based on the Complete Chloroplast Genome Sequence Wang H, Zhang Y, Zhang L, Wang J, Guo H, Zong J, Chen J, Li D, Li L, Liu J, Li J Curr Issues Mol Biol 19-Feb-2024
PMCID:PMC10888139
doi:10.3390/cimb46020106
PMID:38392224
The mechanism of Langchuangding in treatment of systemic lupus erythematosus via modulating TLR7-IRF7-IFNα pathway Wang M, Zhang Y, Zhai Y, Li H, Xie Z, Wen C Heliyon 17-Feb-2024
PMCID:PMC10918011
doi:10.1016/j.heliyon.2024.e26022
PMID:38455571

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Indenes and isoindenes
Coixinden B 9845244 Click to see CC(=O)C1(C=C(C2=C1C=CC(=C2)OC)OC)O 234.25 unknown https://doi.org/10.1271/NOGEIKAGAKU1924.67.1405
> Benzenoids / Phenols / Methoxyphenols
threo-1-C-Syringylglycerol 75492726 Click to see COC1=CC(=CC(=C1O)OC)C(C(CO)O)O 244.24 unknown https://doi.org/10.1016/0031-9422(89)80136-0
> Lignans, neolignans and related compounds / Lignan lactones
4-Ketopinoresinol 44578390 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(89)80136-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1055/S-2006-959500
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1055/S-2006-959500
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1055/S-2006-959500
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1055/S-2006-959500
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1248/CPB.36.3147
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.1248/CPB.36.3147
(Z,6R,9R)-9-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-1-(4-hydroxy-3-methoxyphenyl)-5,6-dimethyldec-1-en-3-one 163193945 Click to see 578.90 unknown https://doi.org/10.1248/CPB.36.3147
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/CPB.36.3147
trans-Feruloyl campestanol 129847772 Click to see CC(CCC(C)C(C)CC(=O)C=CC1=CC(=C(C=C1)O)OC)C2CCC3C2(CCC4C3CCC5C4(CCC(C5)O)C)C 578.90 unknown https://doi.org/10.1248/CPB.36.3147
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163195242 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)C)C 578.90 unknown https://doi.org/10.1248/CPB.36.3147
Campestanyl ferulate 13786591 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)C)C 578.90 unknown https://doi.org/10.1248/CPB.36.3147
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1248/CPB.36.3147
(Z,6S,9R)-9-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-4-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-6-propan-2-yldec-1-en-3-one 163190759 Click to see 592.90 unknown https://doi.org/10.1248/CPB.36.3147
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.36.3147
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1248/CPB.36.3147
trans-Feruloyl stigmastanol 129847783 Click to see CC(C)C(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCCC4)C)C)CC(C(=O)C=CC5=CC(=C(C=C5)O)OC)O 592.90 unknown https://doi.org/10.1248/CPB.36.3147
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1016/0031-9422(89)80136-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-2-amino-3-(5-methyl-3-oxo-1,2-oxazolidin-2-yl)propanoic acid 163188551 Click to see 188.18 unknown https://doi.org/10.1016/S0031-9422(00)82536-4
> Organoheterocyclic compounds / Benzoxazoles / Benzoxazolones
Coixol 10772 Click to see 165.15 unknown https://doi.org/10.1016/S0031-9422(00)80613-5
https://doi.org/10.1021/NP50055A009

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