5-Dehydrokarounidiol

Details

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Internal ID 58ebc67e-651f-4b3e-a8aa-486bffdd1ff1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3R,6aS,6bS,8aS,11R,12aR,14bR)-11-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-1,2,3,7,8,9,10,12,12a,13-decahydropicen-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H46O2/c1-25(2)22-9-8-21-20(28(22,5)12-11-24(25)32)10-13-30(7)23-18-26(3,19-31)14-15-27(23,4)16-17-29(21,30)6/h8-10,23-24,31-32H,11-19H2,1-7H3/t23-,24-,26-,27-,28-,29-,30+/m1/s1
InChI Key WDJWPKSFUUKJFX-CSVNMTLBSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O2
Molecular Weight 438.70 g/mol
Exact Mass 438.349780706 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.98
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Dehydrokarounidiol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.6388 63.88%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6394 63.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9163 91.63%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5635 56.35%
BSEP inhibitior + 0.8449 84.49%
P-glycoprotein inhibitior - 0.6318 63.18%
P-glycoprotein substrate - 0.6205 62.05%
CYP3A4 substrate + 0.6385 63.85%
CYP2C9 substrate - 0.8350 83.50%
CYP2D6 substrate - 0.7620 76.20%
CYP3A4 inhibition - 0.8016 80.16%
CYP2C9 inhibition - 0.8893 88.93%
CYP2C19 inhibition - 0.8457 84.57%
CYP2D6 inhibition - 0.9156 91.56%
CYP1A2 inhibition - 0.8632 86.32%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.6829 68.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6559 65.59%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9568 95.68%
Skin irritation - 0.6560 65.60%
Skin corrosion - 0.9692 96.92%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8832 88.32%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5213 52.13%
skin sensitisation - 0.6103 61.03%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8142 81.42%
Estrogen receptor binding + 0.8015 80.15%
Androgen receptor binding + 0.6842 68.42%
Thyroid receptor binding + 0.7594 75.94%
Glucocorticoid receptor binding + 0.7975 79.75%
Aromatase binding + 0.7706 77.06%
PPAR gamma + 0.6562 65.62%
Honey bee toxicity - 0.8565 85.65%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9677 96.77%

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 95.50% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.76% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.02% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.00% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.19% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.82% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 85.54% 90.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.74% 92.94%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.15% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.02% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 81.05% 94.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.21% 91.71%

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.
Cucumis melo
Trichosanthes kirilowii

Cross-Links

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PubChem 10094697
LOTUS LTS0053905
wikiData Q104389586