beta-Costol

Details

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Internal ID 82221764-0cbf-4185-9daf-e2b17af5cba1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 2-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-en-1-ol
SMILES (Canonical) CC12CCCC(=C)C1CC(CC2)C(=C)CO
SMILES (Isomeric) CC12CCCC(=C)C1CC(CC2)C(=C)CO
InChI InChI=1S/C15H24O/c1-11-5-4-7-15(3)8-6-13(9-14(11)15)12(2)10-16/h13-14,16H,1-2,4-10H2,3H3
InChI Key FKWGZOFNSIESOX-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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beta-Costol
Costol
(+)-.beta.-Costol
515-20-8
b-Costol
.beta.-Costol
(+)-Costol
FKWGZOFNSIESOX-UHFFFAOYSA-N
4(15),11(13)-Eudesmadien-12-ol
Eudesma-4(14),11(13)-dien-12-ol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Costol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.7064 70.64%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.7572 75.72%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.8779 87.79%
OATP1B3 inhibitior + 0.8967 89.67%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8908 89.08%
P-glycoprotein inhibitior - 0.9332 93.32%
P-glycoprotein substrate - 0.8658 86.58%
CYP3A4 substrate + 0.5580 55.80%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate - 0.7388 73.88%
CYP3A4 inhibition - 0.7023 70.23%
CYP2C9 inhibition - 0.6511 65.11%
CYP2C19 inhibition - 0.5690 56.90%
CYP2D6 inhibition - 0.8869 88.69%
CYP1A2 inhibition - 0.7073 70.73%
CYP2C8 inhibition - 0.6895 68.95%
CYP inhibitory promiscuity - 0.5696 56.96%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6195 61.95%
Eye corrosion - 0.9132 91.32%
Eye irritation + 0.6805 68.05%
Skin irritation - 0.7026 70.26%
Skin corrosion - 0.9621 96.21%
Ames mutagenesis - 0.8537 85.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4501 45.01%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5770 57.70%
skin sensitisation + 0.6726 67.26%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7319 73.19%
Acute Oral Toxicity (c) III 0.7974 79.74%
Estrogen receptor binding - 0.7569 75.69%
Androgen receptor binding - 0.5527 55.27%
Thyroid receptor binding - 0.6669 66.69%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.7508 75.08%
PPAR gamma - 0.7812 78.12%
Honey bee toxicity - 0.9228 92.28%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9935 99.35%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.08% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.39% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.17% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 90.05% 95.93%
CHEMBL206 P03372 Estrogen receptor alpha 89.57% 97.64%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.76% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 85.62% 97.79%
CHEMBL237 P41145 Kappa opioid receptor 85.39% 98.10%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.49% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.98% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.71% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.66% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.30% 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.
Aucklandia costus
Ipomoea batatas

Cross-Links

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PubChem 12304104
NPASS NPC288860
LOTUS LTS0079868
wikiData Q67879720