plumbagine F I

Details

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Internal ID bcb5dd29-459f-4c8a-8070-fcd8d314b4f3
Taxonomy Organoheterocyclic compounds > Pyrrolidines > Pyrrolidine carboxylic acids and derivatives > Pyrrolidine carboxylic acids
IUPAC Name (5S,7R,7aR)-2-(2,4-dihydroxybutyl)-3-imino-5-(2-methylprop-1-enyl)-5,6,7,7a-tetrahydro-1H-pyrrolo[1,2-c]imidazole-7-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H25N3O4/c1-9(2)5-10-6-12(14(21)22)13-8-17(15(16)18(10)13)7-11(20)3-4-19/h5,10-13,16,19-20H,3-4,6-8H2,1-2H3,(H,21,22)/t10-,11?,12-,13+/m1/s1
InChI Key VXIDNRDRDTVAPE-ODWCKFRGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H25N3O4
Molecular Weight 311.38 g/mol
Exact Mass 311.18450629 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.09
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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CHEMBL2407431

2D Structure

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2D Structure of plumbagine F I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9005 90.05%
Caco-2 - 0.5628 56.28%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5149 51.49%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9223 92.23%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5396 53.96%
P-glycoprotein inhibitior - 0.9255 92.55%
P-glycoprotein substrate - 0.5710 57.10%
CYP3A4 substrate + 0.5264 52.64%
CYP2C9 substrate - 0.6145 61.45%
CYP2D6 substrate - 0.8274 82.74%
CYP3A4 inhibition - 0.9604 96.04%
CYP2C9 inhibition - 0.8539 85.39%
CYP2C19 inhibition - 0.8365 83.65%
CYP2D6 inhibition - 0.8924 89.24%
CYP1A2 inhibition - 0.7866 78.66%
CYP2C8 inhibition - 0.9120 91.20%
CYP inhibitory promiscuity - 0.9714 97.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5294 52.94%
Eye corrosion - 0.9794 97.94%
Eye irritation - 0.9694 96.94%
Skin irritation - 0.7524 75.24%
Skin corrosion - 0.9008 90.08%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7853 78.53%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5713 57.13%
skin sensitisation - 0.8336 83.36%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6294 62.94%
Acute Oral Toxicity (c) III 0.5933 59.33%
Estrogen receptor binding - 0.5494 54.94%
Androgen receptor binding - 0.5597 55.97%
Thyroid receptor binding - 0.5932 59.32%
Glucocorticoid receptor binding + 0.5518 55.18%
Aromatase binding - 0.7391 73.91%
PPAR gamma + 0.6243 62.43%
Honey bee toxicity - 0.8437 84.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.5191 51.91%

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 98.98% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.55% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.61% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 88.14% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.76% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.30% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.49% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.81% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.69% 96.95%

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.
Plumbago zeylanica

Cross-Links

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PubChem 71746445
LOTUS LTS0166031
wikiData Q105298520