Plaunotol

Details

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Internal ID 47df57a1-d553-4e4d-a831-258fdda83d74
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2Z,6E)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-6-methylocta-2,6-diene-1,8-diol
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCO)C)CO)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC/C(=C/CC/C(=C/CO)/C)/CO)/C)C
InChI InChI=1S/C20H34O2/c1-17(2)8-5-9-18(3)10-6-12-20(16-22)13-7-11-19(4)14-15-21/h8,10,13-14,21-22H,5-7,9,11-12,15-16H2,1-4H3/b18-10+,19-14+,20-13-
InChI Key SUWYPNNPLSRNPS-UNTSEYQFSA-N
Popularity 113 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O2
Molecular Weight 306.50 g/mol
Exact Mass 306.255880323 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.10
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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Kelnac
64218-02-6
Plaunotolum
Plaunotolum [Latin]
CS-684
Plaunotol [INN:JAN]
18-hydroxygeranylgeraniol
(E,Z,E)-7-Hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol
Kelnac (TN)
UNII-MV715X4634
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Plaunotol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9770 97.70%
Caco-2 + 0.7976 79.76%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4632 46.32%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9312 93.12%
OATP1B3 inhibitior + 0.9353 93.53%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7944 79.44%
P-glycoprotein inhibitior - 0.7785 77.85%
P-glycoprotein substrate - 0.9273 92.73%
CYP3A4 substrate - 0.5548 55.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.8614 86.14%
CYP2C9 inhibition - 0.8689 86.89%
CYP2C19 inhibition - 0.8773 87.73%
CYP2D6 inhibition - 0.9119 91.19%
CYP1A2 inhibition - 0.8663 86.63%
CYP2C8 inhibition - 0.9421 94.21%
CYP inhibitory promiscuity - 0.8063 80.63%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6428 64.28%
Eye corrosion + 0.4493 44.93%
Eye irritation + 0.7113 71.13%
Skin irritation - 0.5862 58.62%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3849 38.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.9000 90.00%
skin sensitisation + 0.7769 77.69%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.9420 94.20%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6634 66.34%
Acute Oral Toxicity (c) IV 0.6402 64.02%
Estrogen receptor binding - 0.5488 54.88%
Androgen receptor binding - 0.8008 80.08%
Thyroid receptor binding + 0.6085 60.85%
Glucocorticoid receptor binding - 0.5826 58.26%
Aromatase binding + 0.5993 59.93%
PPAR gamma + 0.8389 83.89%
Honey bee toxicity - 0.9087 90.87%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9391 93.91%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.96% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.95% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.67% 99.17%

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.
Croton stellatopilosus
Croton sublyratus
Trichosanthes kirilowii

Cross-Links

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PubChem 5282197
NPASS NPC140501
LOTUS LTS0163405
wikiData Q27114751