Bohlmann K2604

Details

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Internal ID 11124ae7-58e7-475d-b4c5-02b3f1222d09
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name (2,7-dihydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-yl) 3-methylbut-2-enoate
SMILES (Canonical) CC1CC(CC2C1(CC(C(C2OC(=O)C=C(C)C)O)C(=C)C)C)O
SMILES (Isomeric) CC1CC(CC2C1(CC(C(C2OC(=O)C=C(C)C)O)C(=C)C)C)O
InChI InChI=1S/C20H32O4/c1-11(2)7-17(22)24-19-16-9-14(21)8-13(5)20(16,6)10-15(12(3)4)18(19)23/h7,13-16,18-19,21,23H,3,8-10H2,1-2,4-6H3
InChI Key JGLTUIDSFQWPBH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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BOHLMANN K2604
CHEMBL1988646
NSC-302286
NCI60_002541

2D Structure

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2D Structure of Bohlmann K2604

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.6712 67.12%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8048 80.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9203 92.03%
OATP1B3 inhibitior - 0.2157 21.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4725 47.25%
P-glycoprotein inhibitior - 0.7597 75.97%
P-glycoprotein substrate - 0.6318 63.18%
CYP3A4 substrate + 0.6290 62.90%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.9009 90.09%
CYP3A4 inhibition - 0.6108 61.08%
CYP2C9 inhibition - 0.8629 86.29%
CYP2C19 inhibition - 0.8043 80.43%
CYP2D6 inhibition - 0.9410 94.10%
CYP1A2 inhibition - 0.8642 86.42%
CYP2C8 inhibition - 0.7132 71.32%
CYP inhibitory promiscuity - 0.9139 91.39%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9643 96.43%
Carcinogenicity (trinary) Non-required 0.6607 66.07%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9508 95.08%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9592 95.92%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4862 48.62%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6376 63.76%
skin sensitisation - 0.5353 53.53%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7343 73.43%
Acute Oral Toxicity (c) III 0.7026 70.26%
Estrogen receptor binding + 0.7715 77.15%
Androgen receptor binding - 0.5278 52.78%
Thyroid receptor binding + 0.5638 56.38%
Glucocorticoid receptor binding + 0.7039 70.39%
Aromatase binding - 0.5164 51.64%
PPAR gamma - 0.6167 61.67%
Honey bee toxicity - 0.4661 46.61%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5645 56.45%
Fish aquatic toxicity + 1.0000 100.00%

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 98.01% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.93% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.82% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.68% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.66% 96.77%
CHEMBL340 P08684 Cytochrome P450 3A4 89.79% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.10% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.05% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.92% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.95% 96.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.58% 91.07%
CHEMBL5255 O00206 Toll-like receptor 4 83.36% 92.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.17% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.60% 92.94%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 81.29% 95.71%
CHEMBL2061 P19793 Retinoid X receptor alpha 81.29% 91.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.21% 86.33%
CHEMBL299 P17252 Protein kinase C alpha 80.70% 98.03%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.24% 94.33%

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.
Euryops lateriflorus

Cross-Links

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PubChem 327375
LOTUS LTS0205368
wikiData Q105127516