Plumericidine

Details

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Internal ID ee171048-8fa5-4026-94e1-690e0c73c7ca
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name (7S)-3'-[(1R)-1-hydroxyethyl]spiro[5,6-dihydrocyclopenta[c]pyridine-7,5'-furan]-2'-one
SMILES (Canonical) CC(C1=CC2(CCC3=C2C=NC=C3)OC1=O)O
SMILES (Isomeric) C[C@H](C1=C[C@]2(CCC3=C2C=NC=C3)OC1=O)O
InChI InChI=1S/C13H13NO3/c1-8(15)10-6-13(17-12(10)16)4-2-9-3-5-14-7-11(9)13/h3,5-8,15H,2,4H2,1H3/t8-,13+/m1/s1
InChI Key WMPIWXGTGMOEMD-OQPBUACISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H13NO3
Molecular Weight 231.25 g/mol
Exact Mass 231.08954328 g/mol
Topological Polar Surface Area (TPSA) 59.40 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.09
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Plumericidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.5323 53.23%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8281 82.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9385 93.85%
OATP1B3 inhibitior + 0.9644 96.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6699 66.99%
P-glycoprotein inhibitior - 0.9667 96.67%
P-glycoprotein substrate - 0.8237 82.37%
CYP3A4 substrate - 0.5116 51.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8574 85.74%
CYP3A4 inhibition - 0.6321 63.21%
CYP2C9 inhibition - 0.7173 71.73%
CYP2C19 inhibition - 0.5413 54.13%
CYP2D6 inhibition - 0.8640 86.40%
CYP1A2 inhibition + 0.6384 63.84%
CYP2C8 inhibition - 0.7045 70.45%
CYP inhibitory promiscuity - 0.7458 74.58%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4127 41.27%
Eye corrosion - 0.9770 97.70%
Eye irritation - 0.6145 61.45%
Skin irritation - 0.7048 70.48%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7749 77.49%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5166 51.66%
skin sensitisation - 0.6536 65.36%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8185 81.85%
Acute Oral Toxicity (c) III 0.4168 41.68%
Estrogen receptor binding - 0.7399 73.99%
Androgen receptor binding - 0.6992 69.92%
Thyroid receptor binding - 0.5710 57.10%
Glucocorticoid receptor binding + 0.6471 64.71%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.7868 78.68%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.6593 65.93%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.39% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.32% 96.09%
CHEMBL301 P24941 Cyclin-dependent kinase 2 90.21% 91.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.94% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 86.69% 91.49%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.56% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.43% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.74% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.06% 99.23%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.74% 85.30%
CHEMBL5896 O75164 Lysine-specific demethylase 4A 82.74% 99.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.87% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 81.67% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.09% 95.56%
CHEMBL4208 P20618 Proteasome component C5 80.26% 90.00%

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.
Acacia salicina
Achillea santolinoides subsp. wilhelmsii
Ajania nubigena
Backhousia angustifolia
Blighia welwitschii
Cunninghamia konishii
Dioscorea villosa
Juniperus ashei
Kalanchoe blossfeldiana
Plumeria rubra
Sassafras albidum

Cross-Links

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PubChem 45101897
NPASS NPC132747
LOTUS LTS0100089
wikiData Q105308750