(Q15411006)

HARMANE (English)

5 October 2016

C₁₂H₁₀N₂

1 reference

HARMANE (English)

5 October 2016

CC1=NC=CC2=C1NC3=CC=CC=C23

1 reference

Recon 2.2: from reconstruction to model of human metabolism

HARMANE (English)

5 October 2016

1 reference

Strychnos usambarensis

1 reference

Qualitative and quantitative evaluation of bisindole usambarane alkaloids inStrychnos usambarensis roots by high performance liquid chromatography-diode-array

Prunus dulcis

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Cashew

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Polygala tenuifolia

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

β-Carboline alkaloids ofPolygala tenuifolia

Passiflora incarnata

4 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

IDENTIFICATION AND SIMULTANEOUS ANALYSIS OF HARMANE, HARMINE, HARMOL, ISOVITEXIN, AND VITEXIN INPASSIFLORA INCARNATAEXTRACTS WITH A NOVEL HPLC METHOD

Juglans regia

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Pinellia ternata

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Areca catechu

2 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Great yellow gentian

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Tribulus terrestris

3 references

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Locomotor effects in sheep of alkaloids identified in Australian Tribulus terrestris

Carex brevicollis

2 references

Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968

1,4-Substituted b-Carbolines from Carex brevicollis DC

Cephalanthus natalensis

1 reference

The Chemotaxonomic Significance of Alkaloids in the Naucleeae S.L. (Rubiaceae)

Mitragyna hirsuta

1 reference

The Chemotaxonomic Significance of Alkaloids in the Naucleeae S.L. (Rubiaceae)

Cribricellina cribraria

1 reference

New cytotoxic beta-carboline alkaloids from the marine bryozoan, Cribricellina cribraria

Passiflora alata

2 references

Pharmacological trials of crude extract of Passiflora alata

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Symplocos setchuensis

1 reference

Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives

Crocus sativus

1 reference

Antityrosinase principles and constituents of the petals of Crocus sativus

Kopsia griffithii

2 references

Leishmanicidal alkaloids from Kopsia griffithii

Alkaloids from Kopsia griffithii

Ophiorrhiza japonica

2 references

Structure of ophiorines A and B; novel type gluco indole alkaloids isolated from ophiorrhiza spp.

[Studies on the constituents of Ophiorrhiza japonica Bl]

Ophiorrhiza liukiuensis

2 references

Camptothecins and two new monoterpene glucosides from Ophiorrhiza liukiuensis

Structure of ophiorines A and B; novel type gluco indole alkaloids isolated from ophiorrhiza spp.

Peganum harmala

2 references

Antibacterial and antifungal activities of (beta)-carboline alkaloids of Peganum harmala (L) seeds and their combination effects.

Accumulation of beta-Carboline Alkaloids and Serotonin by Cell Cultures of Peganum harmala L: I. CORRELATION BETWEEN PLANTS AND CELL CULTURES AND INFLUENCE OF MEDIUM CONSTITUENTS

Acraea andromacha

1 reference

High-performance liquid chromatographic identification of simple β-carboline alkaloids in specimens of heliconiini butterflies

Bupleurum falcatum

1 reference

Commelina communis

1 reference

Anticariogenic β-carboline alkaloids fromCommelina communis

Costaticella bicuspis

1 reference

β-Carboline Alkaloids from the Marine Bryozoan Costaticella hastata

Croton moritibensis

1 reference

Alkaloids and Diterpenes FromCroton moritibensis

Euodia rutaecarpa

1 reference

Gentiana

1 reference

Grewia bicolor

1 reference

Investigation of Grewia bicolor Juss

Guiera senegalensis

1 reference

Antimalarial activity of extracts and alkaloids isolated from six plants used in traditional medicine in Mali and Sao Tome

Nicotiana tabacum

1 reference

The isolation of harmane and norharmane from tobacco and cigarette smoke

Nocardia

1 reference

Isolation of harman and norharman from Nocardia sp. and their inhibitory activity against plant seedlings.

Ophiopogon

1 reference

Panax ginseng

2 references

A thiazole and two β-carboline constitutents fromPanax ginseng

Passiflora actinia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora boenderi

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora caerulea

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora citrina

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora edulis

3 references

Four cycloartane triterpenoids and six related saponins from Passiflora edulis

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Pharmacochemical investigations on raw materials genus passiflora. 3. Phytochemical investigations on raw materials of passiflora edulis forma flavicarpa (author's transl)

Passiflora foetida

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora guatemalensis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora jorullensis

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora macrophylla

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora menispermifolia

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora multiflora

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora perfoliata

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora rubra

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora sexflora

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Passiflora xiikzodz

1 reference

High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora

Polygala

1 reference

Pyricularia oryzae

1 reference

Secondary metabolites of Pyricularia oryzae II. Polyketide metabolites

Rauvolfia sellowii

1 reference

Alkaloids of Rauwolfia sellowii

Rauvolfia sumatrana

1 reference

Novel Indole Alkaloids from the Leaves of Rauwolfia sumatrana JACK. in Thailand.

Schisandra chinensis

1 reference

Simira mexicana

1 reference

Alkaloids from Gelsemium elegans

Simira salvadorensis

1 reference

Phototoxic substances from Flaveria trinervis and Simira salvadorensis

Strychnos johnsonii

1 reference

Alkaloids of Strychnos johnsonii

Zingiber officinale

1 reference

Streptomyces nigra

1 reference

Streptomyces nigra sp. nov. Is a Novel Actinobacterium Isolated From Mangrove Soil and Exerts a Potent Antitumor Activity in Vitro

Phyllodium pulchellum

1 reference

Chemical and pharmacological evaluation of Desmodium pulchellum

Nauclea diderrichii

1 reference

The Constituents of Naucleadiderrichii. Part II. Isolation and Classification of Constituents; Simple β-Carboline and Pyridine Alkaloids

Noctiluca miliaris

1 reference

TRACE CHARACTERIZATION OF THE FLUORESCENT SUBSTANCES OF A DINOFLAGELLATE,NOCTILUCA MILIARIS

Noctiluca scintillans

1 reference

TRACE CHARACTERIZATION OF THE FLUORESCENT SUBSTANCES OF A DINOFLAGELLATE,NOCTILUCA MILIARIS

Simira eliezeriana

1 reference

Simiranes A and B: erythroxylanes diterpenes and other compounds from Simira eliezeriana (Rubiaceae).

Uncaria elliptica

1 reference

Triterpenoidal constituents of uncaria florida vidal

Uncaria rhynchophylla

1 reference

Triterpenoidal constituents of uncaria florida vidal

Phaseolus vulgaris

1 reference

Metabolite Profiling of Root Exudates of Common Bean under Phosphorus Deficiency

Paracribricellina cribraria

1 reference

New cytotoxic beta-carboline alkaloids from the marine bryozoan, Cribricellina cribraria

Symplocos theifolia

1 reference

Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives

Ophiorrhiza kuroiwae

2 references

Camptothecins and two new monoterpene glucosides from Ophiorrhiza liukiuensis

Structure of ophiorines A and B; novel type gluco indole alkaloids isolated from ophiorrhiza spp.

Croton heliotropiifolius

1 reference

Alkaloids and Diterpenes FromCroton moritibensis

Prunus avium

1 reference

Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection

Grewia damine

1 reference

Investigation of Grewia bicolor Juss

1 reference

1 reference

Medical Subject Headings

15 March 2018

1 reference

Medical Subject Headings

15 March 2018

Harmane

0 references

Identifiers

InChI

InChI=1S/C12H10N2/c1-8-12-10(6-7-13-8)9-4-2-3-5-11(9)14-12/h2-7,14H,1H3

1 reference

HARMANE (English)

5 October 2016

2 references

HARMANE (English)

5 October 2016

ChEBI release 2020-09-01

2 references

harman (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=486-84-0

10 April 2021

1 reference

Harmane (English)

5 October 2016

2 references

HARMANE (English)

5 October 2016

Reaxys registry number

143898

1 reference

harman (English)

5 October 2016

mapping relation type

2 references

harman (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C12H10N2/c1-8-12-10(6-7-13-8)9-4-2-3-5-11(9)14-12/h2-7,14H,1H3

1 reference

HARMAN (English)

5 October 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP000786

1 reference

MassBank accession ID

0 references

MSBNK-Fiocruz-FIO00110

0 references

MSBNK-Fiocruz-FIO00111

0 references

MSBNK-Fiocruz-FIO00112

0 references

MSBNK-Fiocruz-FIO00113

0 references

MSBNK-Fiocruz-FIO00114

0 references

MSBNK-Fiocruz-FIO00115

0 references

MSBNK-Fiocruz-FIO00116

0 references

MSBNK-Fiocruz-FIO00117

0 references

MSBNK-Fiocruz-FIO00118

0 references

MSBNK-Fiocruz-FIO00119

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000084

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000085

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000086

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000087

0 references

MSBNK-UFZ-UA000701

0 references

MSBNK-UFZ-UA000702

0 references

MSBNK-Washington_State_Univ-BML81360

0 references

MSBNK-Washington_State_Univ-BML81361

0 references

MSBNK-Washington_State_Univ-BML81362

0 references

MSBNK-Washington_State_Univ-BML81363

0 references

MSBNK-IPB_Halle-PB000886

0 references

MSBNK-IPB_Halle-PB000901

0 references

MSBNK-IPB_Halle-PB003741

0 references

MSBNK-IPB_Halle-PB005765

0 references

MSBNK-IPB_Halle-PB005781

0 references

MSBNK-IPB_Halle-PB005782

0 references

MSBNK-IPB_Halle-PB005783

0 references

MSBNK-IPB_Halle-PB005784

0 references

MSBNK-Keio_Univ-KO001028

0 references

MSBNK-Keio_Univ-KO001029

0 references

MSBNK-Keio_Univ-KO001030

0 references

MSBNK-Keio_Univ-KO001031

0 references

MSBNK-Keio_Univ-KO001032

0 references

MSBNK-Keio_Univ-KO003103

0 references

MSBNK-Keio_Univ-KO003104

0 references

MSBNK-Keio_Univ-KO003105

0 references

MSBNK-Keio_Univ-KO003106

0 references

MSBNK-Keio_Univ-KO003107

0 references

SPLASH

splash10-001i-0900000000-b61926dd87fa8a8bf547

0 references

splash10-001i-0900000000-be2b3d6251e5698ec184

0 references

splash10-001i-0900000000-2467a87546dc5758f74c

0 references

splash10-014i-0900000000-6222b796373c7d683edd

0 references

splash10-014i-0900000000-5f9fc354bf2eb82f440c

0 references

splash10-001i-0900000000-8a722b1b5d7b5941896b

0 references

splash10-001i-0900000000-c3e22e3a50c1a33d3313

0 references

splash10-001i-0900000000-da3abe12c596a25c4fc7

0 references

splash10-00lr-0900000000-a0630fe37a9dae900711

0 references

splash10-014i-0900000000-fe40ad28de7c40fde973

0 references

splash10-001i-0900000000-8f767ae14c8cb390abd4

0 references

splash10-001i-0900000000-3206fb22991bbadfb410

0 references

splash10-014i-0900000000-fbe37bd173c6820a5fbf

0 references

splash10-001i-0900000000-493e054134592fad2cd8

0 references

splash10-001i-0900000000-e1101c121f5e3a8ec067

0 references

splash10-001i-0900000000-181c3a8132c8bd7c42ac

0 references

splash10-001i-0900000000-f782ac14295437be4ac3

0 references

splash10-0159-0900000000-0d6bdc509aa56c58b092

0 references

splash10-001i-0900000000-2c091f7fb293a5702807

0 references

splash10-001i-2900000000-37a11b66e75cedf3e072

0 references

splash10-001i-2900000000-753e83180abd8e8f4306

0 references

splash10-053r-4900000000-a0c45efe16d695cf0465

0 references

splash10-03di-2900000000-4e2e84a5d7cb4f3b6e5a

0 references

splash10-001i-0900000000-eeae7e4ae0e57f17ea4e

0 references

splash10-001i-0900000000-b99788a07a287e8b9126

0 references

splash10-001i-0900000000-44b48ea4f06e0ee29093

0 references

splash10-014i-0900000000-ca32c2e8de7f8959e1de

0 references

splash10-014i-1900000000-da421e616428bd2e0f49

0 references

splash10-001i-0900000000-846c2af94f8b7aaaa069

0 references

splash10-001i-0900000000-c00da62a33265fe80daa

0 references

splash10-001i-1900000000-fa8275cdabb2ecc88a13

0 references

splash10-001i-0900000000-25b831923d148f16d3c2

0 references

splash10-001i-0900000000-5ebce9e576bf322bfd6f

0 references

splash10-001i-0900000000-905be1cd27ff26389d27

0 references

splash10-001i-0900000000-37bf6aca7a977e467e35

0 references

splash10-001i-0900000000-da5f8f71b14a2afaf96b

0 references

NMRShiftDB structure ID

10018197

1 reference

DSSTox substance ID

DTXSID80197568

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

UNII

82D6J0535P

HARMAN (English)

ECHA Substance Infocard ID

5 October 2016

100.006.948

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Harman (English)

CAS no.: 486-84-0 (English)

1 reference

harman

1 reference

Medical Subject Headings

MeSH descriptor ID

C005010

Human Metabolome Database ID

14 March 2018

HMDB0035196

2 references

based on heuristic

inferred from InChIKey

3 references

harman (English)

5 October 2016

inferred from InChIKey

UNII

82D6J0535P

2 references

Global Substance Registration System

UNII

82D6J0535P

HARMAN (English)

5 October 2016

0 references

1 reference