Dalnigrin

Details

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Internal ID 5c6cad0c-75e1-45b4-9a6c-ca7f8d6705c8
Taxonomy Phenylpropanoids and polyketides > Neoflavonoids > Neoflavones
IUPAC Name 6-hydroxy-7-methoxy-4-(4-methoxyphenyl)chromen-2-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=CC(=O)OC3=CC(=C(C=C23)O)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C2=CC(=O)OC3=CC(=C(C=C23)O)OC
InChI InChI=1S/C17H14O5/c1-20-11-5-3-10(4-6-11)12-8-17(19)22-15-9-16(21-2)14(18)7-13(12)15/h3-9,18H,1-2H3
InChI Key VGFANVFKVOTCIW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O5
Molecular Weight 298.29 g/mol
Exact Mass 298.08412354 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dalnigrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9733 97.33%
Caco-2 + 0.9396 93.96%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7509 75.09%
OATP2B1 inhibitior - 0.5882 58.82%
OATP1B1 inhibitior + 0.9269 92.69%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5415 54.15%
P-glycoprotein inhibitior + 0.6095 60.95%
P-glycoprotein substrate - 0.8568 85.68%
CYP3A4 substrate + 0.5301 53.01%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.6847 68.47%
CYP2C9 inhibition - 0.6315 63.15%
CYP2C19 inhibition - 0.5811 58.11%
CYP2D6 inhibition - 0.9055 90.55%
CYP1A2 inhibition + 0.5316 53.16%
CYP2C8 inhibition + 0.6306 63.06%
CYP inhibitory promiscuity - 0.5084 50.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5671 56.71%
Eye corrosion - 0.9750 97.50%
Eye irritation + 0.7635 76.35%
Skin irritation - 0.6468 64.68%
Skin corrosion - 0.9811 98.11%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6388 63.88%
Micronuclear + 0.9059 90.59%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.9516 95.16%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6117 61.17%
Acute Oral Toxicity (c) II 0.5637 56.37%
Estrogen receptor binding + 0.9002 90.02%
Androgen receptor binding + 0.9274 92.74%
Thyroid receptor binding + 0.7018 70.18%
Glucocorticoid receptor binding + 0.9455 94.55%
Aromatase binding + 0.8539 85.39%
PPAR gamma + 0.8864 88.64%
Honey bee toxicity - 0.9134 91.34%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.9330 93.30%

Targets

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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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.37% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.17% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.11% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.52% 99.15%
CHEMBL2581 P07339 Cathepsin D 94.33% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 93.10% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.76% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.13% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.09% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.19% 86.92%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.65% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.64% 99.23%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 85.86% 95.53%
CHEMBL4208 P20618 Proteasome component C5 82.11% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.99% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.91% 95.50%
CHEMBL2535 P11166 Glucose transporter 81.19% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.80% 96.09%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.41% 80.78%

Plants that contains it

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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.
Arnica longifolia
Dalbergia nigra
Kaempferia galanga
Rubus rigidus

Cross-Links

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PubChem 91279357
NPASS NPC182087
LOTUS LTS0249035
wikiData Q105285763