Dictamnine

Details

Top
Internal ID e5843dd7-b00d-49c1-8c52-e39763c4f620
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Furanoquinolines
IUPAC Name 4-methoxyfuro[2,3-b]quinoline
SMILES (Canonical) COC1=C2C=COC2=NC3=CC=CC=C31
SMILES (Isomeric) COC1=C2C=COC2=NC3=CC=CC=C31
InChI InChI=1S/C12H9NO2/c1-14-11-8-4-2-3-5-10(8)13-12-9(11)6-7-15-12/h2-7H,1H3
InChI Key WIONIXOBNMDJFJ-UHFFFAOYSA-N
Popularity 210 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H9NO2
Molecular Weight 199.20 g/mol
Exact Mass 199.063328530 g/mol
Topological Polar Surface Area (TPSA) 35.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
484-29-7
Dictamine
4-Methoxyfuro[2,3-b]quinoline
Furo[2,3-b]quinoline, 4-methoxy-
CCRIS 1583
Dictamnine;Dectamine
Furo(2,3-b)quinoline, 4-methoxy-
BRN 0176932
UNII-HQZ3798D0A
C12H9NO2
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Dictamnine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6954 69.54%
Blood Brain Barrier + 0.8379 83.79%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5486 54.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9580 95.80%
OATP1B3 inhibitior + 0.9737 97.37%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6426 64.26%
P-glycoprotein inhibitior - 0.9269 92.69%
P-glycoprotein substrate - 0.9625 96.25%
CYP3A4 substrate - 0.5855 58.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3562 35.62%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.6181 61.81%
CYP2D6 inhibition - 0.8713 87.13%
CYP1A2 inhibition + 0.9820 98.20%
CYP2C8 inhibition + 0.6197 61.97%
CYP inhibitory promiscuity - 0.5866 58.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.3882 38.82%
Eye corrosion - 0.9828 98.28%
Eye irritation + 0.8254 82.54%
Skin irritation - 0.7916 79.16%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis + 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation - 0.7633 76.33%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6213 62.13%
Acute Oral Toxicity (c) III 0.6757 67.57%
Estrogen receptor binding + 0.7823 78.23%
Androgen receptor binding + 0.6514 65.14%
Thyroid receptor binding + 0.6288 62.88%
Glucocorticoid receptor binding + 0.6302 63.02%
Aromatase binding + 0.7722 77.22%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9104 91.04%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity - 0.8738 87.38%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.55% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.63% 91.11%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 91.51% 94.03%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 90.32% 89.44%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.03% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.01% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.99% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.73% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.30% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.08% 94.73%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Acronychia pedunculata
Acronychia pubescens
Aframomum daniellii
Agave deserti
Ageratina saltillensis
Aglaia silvestris
Alchornea cordifolia
Andreadoxa flava
Angelica sinensis
Arachniodes mutica
Asclepias subulata
Atalantia wightii
Balanophora japonica
Boenninghausenia albiflora
Boronia inornata
Boronia pinnata
Bouchardatia neurococca
Bulbine asphodeloides
Celastrus monospermus
Chorilaena quercifolia
Cicer cuneatum
Clausena anisata
Comptonella sessilifoliola
Conium maculatum
Corydalis persica
Corynanthe pachyceras
Cota tinctoria
Croton hutchinsonianus
Cynoglossum amabile
Daphne tangutica
Decatropis bicolor
Delphinium speciosum
Dictamnus albus
Dictamnus dasycarpus
Drummondita calida
Esenbeckia berlandieri subsp. litoralis
Esenbeckia febrifuga
Esenbeckia hartmanii
Esenbeckia leiocarpa
Euonymus europaeus
Eutrochium purpureum
Ficus conraui
Flueggea virosa subsp. virosa
Geijera balansae
Gentianella amarella subsp. acuta
Glinus oppositifolius
Glycosmis angustifolia
Glycosmis mauritiana
Glycosmis pseudoracemosa
Grewia villosa
Griselinia scandens
Gutenbergia cordifolia var. marginata
Halfordia kendack
Haplophyllum acutifolium
Haplophyllum bucharicum
Haplophyllum bungei
Haplophyllum cappadocicum
Haplophyllum dauricum
Haplophyllum griffithianum
Haplophyllum myrtifolium
Haplophyllum obtusifolium
Haplophyllum ramosissimum
Haplophyllum vulcanicum
Helicia nilagirica
Hibiscus tilliaceus
Hortia brasiliana
Hortia longifolia
Hortonia floribunda
Hosta sieboldiana
Inula salsoloides
Iphiona grantioides
Ipomoea carnea
Iris sanguinea
Jacobaea cannabifolia
Jasione montana
Juniperus horizontalis
Jurinea maxima
Lathyrus tingitanus
Lepidaploa lilacina
Machilus zuihoensis
Melicope semecarpifolia
Melicope triphylla
Mesosphaerum urticodes
Millettia pachycarpa
Monachosorum maximowiczii
Morinda coreia
Mycetia nutans
Myrtopsis macrocarpa
Myrtopsis sellingii
Nardia scalaris
Passiflora morifolia
Persicaria tinctoria
Phellodendron amurense
Pilocarpus grandiflorus
Pitavia punctata
Plectranthus caninus
Podocalyx loranthoides
Psiadia anchusifolia
Pycnarrhena novoguineensis
Raputia praetermissa
Raputiarana heptaphylla
Rauvolfia salicifolia
Rhododendron edgeworthii
Rosa transmorrisonensis
Ruta chalepensis
Ruta corsica
Ruta graveolens
Ruta montana
Salta triflora
Salvia polystachya
Sarcomelicope argyrophylla
Sarcomelicope megistophylla
Sideritis perfoliata
Skimmia japonica
Skimmia laureola
Solanum spirale
Sophora leachiana
Spiranthera odoratissima
Strychnos potatorum
Strychnos spinosa
Tetradium glabrifolium
Tetradium trichotomum
Ticorea longiflora
Toddalia asiatica
Trifolium montanum
Trixis grisebachii
Vepris natalensis
Vepris trichocarpa
Vernonia chloropappa
Vicia balansae
Vitellaria paradoxa
Yucca elata
Zanthoxylum ailanthoides
Zanthoxylum armatum
Zanthoxylum austrosinense
Zanthoxylum avicennae
Zanthoxylum beecheyanum
Zanthoxylum caribaeum subsp. rugosum
Zanthoxylum dimorphophyllum
Zanthoxylum ekmanii
Zanthoxylum integrifoliolum
Zanthoxylum mayu
Zanthoxylum nitidum
Zanthoxylum schinifolium
Zanthoxylum simulans
Zanthoxylum wutaiense

Cross-Links

Top
PubChem 68085
NPASS NPC269367
ChEMBL CHEMBL22533
LOTUS LTS0266561
wikiData Q27106403