Powelline, 1,2-dihydro-

Details

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Internal ID 0c8870da-0ffa-4c49-9fad-c5fa17a8e4fc
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Crinine- and Haemanthamine-type amaryllidaceae alkaloids
IUPAC Name 9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-trien-15-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H21NO4/c1-20-15-11-8-18-5-4-17(3-2-10(19)6-14(17)18)12(11)7-13-16(15)22-9-21-13/h7,10,14,19H,2-6,8-9H2,1H3
InChI Key BYIVXRUZAMYOPQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H21NO4
Molecular Weight 303.35 g/mol
Exact Mass 303.14705815 g/mol
Topological Polar Surface Area (TPSA) 51.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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7-Methoxycrinan-3-ol #
BYIVXRUZAMYOPQ-UHFFFAOYSA-N

2D Structure

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2D Structure of Powelline, 1,2-dihydro-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9739 97.39%
Caco-2 + 0.8186 81.86%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.5925 59.25%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9255 92.55%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6099 60.99%
BSEP inhibitior + 0.6375 63.75%
P-glycoprotein inhibitior - 0.8655 86.55%
P-glycoprotein substrate - 0.5687 56.87%
CYP3A4 substrate + 0.6197 61.97%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate + 0.6385 63.85%
CYP3A4 inhibition + 0.6794 67.94%
CYP2C9 inhibition - 0.8971 89.71%
CYP2C19 inhibition - 0.5833 58.33%
CYP2D6 inhibition + 0.5693 56.93%
CYP1A2 inhibition - 0.7427 74.27%
CYP2C8 inhibition - 0.7450 74.50%
CYP inhibitory promiscuity - 0.8627 86.27%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5345 53.45%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.9098 90.98%
Skin irritation - 0.7904 79.04%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.5524 55.24%
Human Ether-a-go-go-Related Gene inhibition + 0.6501 65.01%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8284 82.84%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.6000 60.00%
Acute Oral Toxicity (c) III 0.5348 53.48%
Estrogen receptor binding - 0.5286 52.86%
Androgen receptor binding + 0.5840 58.40%
Thyroid receptor binding + 0.6422 64.22%
Glucocorticoid receptor binding + 0.7617 76.17%
Aromatase binding - 0.7446 74.46%
PPAR gamma + 0.5737 57.37%
Honey bee toxicity - 0.7747 77.47%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.7476 74.76%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.72% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.27% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.52% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.64% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.21% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.17% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.14% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.10% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.84% 91.03%
CHEMBL4208 P20618 Proteasome component C5 83.94% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.41% 100.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.05% 99.18%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 82.08% 80.96%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.79% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.64% 89.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.32% 82.67%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.05% 90.71%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.60% 82.38%

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.
Ammocharis tinneana

Cross-Links

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PubChem 627523
LOTUS LTS0167792
wikiData Q104949385