Papuaforin C

Details

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Internal ID 9583e144-d536-4d8e-a5c7-9bfecbebc317
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids
IUPAC Name (1S,9R,11R)-1,4,4,10,10-pentamethyl-9-(2-methylbutanoyl)-11-(3-methylbut-2-enyl)-3-oxatricyclo[7.3.1.02,7]trideca-2(7),5-diene-8,13-dione
SMILES (Canonical) CCC(C)C(=O)C12C(=O)C3=C(C(C1=O)(CC(C2(C)C)CC=C(C)C)C)OC(C=C3)(C)C
SMILES (Isomeric) CCC(C)C(=O)[C@@]12C(=O)C3=C([C@@](C1=O)(C[C@H](C2(C)C)CC=C(C)C)C)OC(C=C3)(C)C
InChI InChI=1S/C27H38O4/c1-10-17(4)20(28)27-21(29)19-13-14-24(5,6)31-22(19)26(9,23(27)30)15-18(25(27,7)8)12-11-16(2)3/h11,13-14,17-18H,10,12,15H2,1-9H3/t17?,18-,26+,27-/m1/s1
InChI Key CIMLTJLAJZUYBN-DAYBPDHMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O4
Molecular Weight 426.60 g/mol
Exact Mass 426.27700969 g/mol
Topological Polar Surface Area (TPSA) 60.40 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.77
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEMBL509789
(1S,9R,11R)-1,4,4,10,10-Pentamethyl-9-(2-methylbutanoyl)-11-(3-methylbut-2-enyl)-3-oxatricyclo[7.3.1.02,7]trideca-2(7),5-diene-8,13-dione

2D Structure

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2D Structure of Papuaforin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.6799 67.99%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5501 55.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8354 83.54%
OATP1B3 inhibitior + 0.9703 97.03%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7839 78.39%
P-glycoprotein inhibitior - 0.4404 44.04%
P-glycoprotein substrate - 0.5259 52.59%
CYP3A4 substrate + 0.6281 62.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8648 86.48%
CYP3A4 inhibition - 0.6019 60.19%
CYP2C9 inhibition - 0.6616 66.16%
CYP2C19 inhibition - 0.7058 70.58%
CYP2D6 inhibition - 0.9147 91.47%
CYP1A2 inhibition - 0.6401 64.01%
CYP2C8 inhibition - 0.6882 68.82%
CYP inhibitory promiscuity + 0.5794 57.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Non-required 0.5647 56.47%
Eye corrosion - 0.9820 98.20%
Eye irritation - 0.8382 83.82%
Skin irritation - 0.5568 55.68%
Skin corrosion - 0.9193 91.93%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8084 80.84%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6551 65.51%
skin sensitisation - 0.5562 55.62%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.5863 58.63%
Acute Oral Toxicity (c) III 0.7203 72.03%
Estrogen receptor binding + 0.8454 84.54%
Androgen receptor binding + 0.5507 55.07%
Thyroid receptor binding + 0.7483 74.83%
Glucocorticoid receptor binding + 0.6454 64.54%
Aromatase binding + 0.6978 69.78%
PPAR gamma + 0.7471 74.71%
Honey bee toxicity - 0.8405 84.05%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9879 98.79%

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 97.67% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.88% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.30% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.66% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.75% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.10% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.02% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.52% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 86.26% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.28% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.89% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.54% 95.71%
CHEMBL4208 P20618 Proteasome component C5 83.53% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 83.40% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 81.05% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.88% 92.62%

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.
Hypericum papuanum

Cross-Links

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PubChem 10993623
NPASS NPC213636