CID 15548652

Details

Top
Internal ID 6a427e34-3a28-4763-b52a-7a6c3fe1f0ef
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC1C(=O)C(C2C(CCCC2(C13CCC4(O3)COC=C4)C)(C)C)OC(=O)C
SMILES (Isomeric) C[C@@H]1C(=O)[C@H]([C@@H]2[C@@]([C@@]13CC[C@]4(O3)COC=C4)(CCCC2(C)C)C)OC(=O)C
InChI InChI=1S/C22H32O5/c1-14-16(24)17(26-15(2)23)18-19(3,4)7-6-8-20(18,5)22(14)10-9-21(27-22)11-12-25-13-21/h11-12,14,17-18H,6-10,13H2,1-5H3/t14-,17-,18+,20+,21-,22-/m1/s1
InChI Key FKTKIKZTYBWJGJ-HQGXMBNISA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H32O5
Molecular Weight 376.50 g/mol
Exact Mass 376.22497412 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.80
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 15548652

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.6217 62.17%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8227 82.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8340 83.40%
OATP1B3 inhibitior + 0.8763 87.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.6079 60.79%
P-glycoprotein inhibitior + 0.6863 68.63%
P-glycoprotein substrate - 0.6526 65.26%
CYP3A4 substrate + 0.6491 64.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8551 85.51%
CYP3A4 inhibition - 0.7956 79.56%
CYP2C9 inhibition - 0.8364 83.64%
CYP2C19 inhibition - 0.8389 83.89%
CYP2D6 inhibition - 0.9478 94.78%
CYP1A2 inhibition - 0.8902 89.02%
CYP2C8 inhibition - 0.5662 56.62%
CYP inhibitory promiscuity - 0.9002 90.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5014 50.14%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9326 93.26%
Skin irritation - 0.6496 64.96%
Skin corrosion - 0.9054 90.54%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7426 74.26%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4795 47.95%
Acute Oral Toxicity (c) III 0.5490 54.90%
Estrogen receptor binding + 0.8630 86.30%
Androgen receptor binding + 0.6485 64.85%
Thyroid receptor binding + 0.7013 70.13%
Glucocorticoid receptor binding + 0.7853 78.53%
Aromatase binding + 0.7062 70.62%
PPAR gamma + 0.6279 62.79%
Honey bee toxicity - 0.8089 80.89%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9932 99.32%

Targets

Top

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 96.36% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.70% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.04% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.44% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.67% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.71% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.34% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.54% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.98% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.62% 82.69%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.17% 81.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.28% 93.04%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.54% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.14% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 82.81% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.80% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.80% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.62% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.98% 95.89%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.39% 95.71%

Plants that contains it

Top
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.
Harrisonia perforata
Otostegia fruticosa
Rydingia integrifolia

Cross-Links

Top
PubChem 15548652
LOTUS LTS0140465
wikiData Q104919989