Paucinervin D

Details

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Internal ID 29638efc-40da-4429-9413-e35b95515497
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 2,5-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromene-7,8-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H40O3/c1-19(2)10-7-11-20(3)12-8-13-21(4)14-9-16-27(6)17-15-23-22(5)18-24(28)25(29)26(23)30-27/h10,12,14,18,28-29H,7-9,11,13,15-17H2,1-6H3/b20-12+,21-14+
InChI Key BTLRXKRGQQIJSD-KDXVVQHGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H40O3
Molecular Weight 412.60 g/mol
Exact Mass 412.29774513 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 8.20
Atomic LogP (AlogP) 7.69
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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RefChem:170208
CHEMBL1254111

2D Structure

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2D Structure of Paucinervin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9778 97.78%
Caco-2 + 0.4948 49.48%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7176 71.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8709 87.09%
OATP1B3 inhibitior + 0.9659 96.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8577 85.77%
P-glycoprotein inhibitior + 0.6436 64.36%
P-glycoprotein substrate - 0.8710 87.10%
CYP3A4 substrate + 0.6069 60.69%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate + 0.4455 44.55%
CYP3A4 inhibition - 0.8608 86.08%
CYP2C9 inhibition - 0.7197 71.97%
CYP2C19 inhibition - 0.5103 51.03%
CYP2D6 inhibition - 0.8748 87.48%
CYP1A2 inhibition + 0.5375 53.75%
CYP2C8 inhibition - 0.6070 60.70%
CYP inhibitory promiscuity - 0.5863 58.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6867 68.67%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8235 82.35%
Skin irritation - 0.6688 66.88%
Skin corrosion - 0.9303 93.03%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7503 75.03%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5476 54.76%
skin sensitisation - 0.7196 71.96%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7541 75.41%
Acute Oral Toxicity (c) III 0.6047 60.47%
Estrogen receptor binding + 0.6678 66.78%
Androgen receptor binding + 0.6207 62.07%
Thyroid receptor binding + 0.6938 69.38%
Glucocorticoid receptor binding + 0.6726 67.26%
Aromatase binding + 0.7560 75.60%
PPAR gamma + 0.8400 84.00%
Honey bee toxicity - 0.9114 91.14%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9911 99.11%

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 99.75% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.73% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.84% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.97% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.82% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.05% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.44% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.57% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.47% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.29% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.86% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.34% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.01% 91.24%

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.
Garcinia paucinervis

Cross-Links

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PubChem 52949815
NPASS NPC469907
ChEMBL CHEMBL1254111
LOTUS LTS0272599
wikiData Q104945722