Caseargrewins G

Details

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Internal ID 78337c1a-1275-4474-9800-2d48da430a87
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Colensane and clerodane diterpenoids
IUPAC Name [(1S,3S,5R,6aS,7R,8R,10S,10aS)-1-acetyloxy-10-hydroxy-3-methoxy-7,8-dimethyl-7-[(2Z)-3-methylpenta-2,4-dienyl]-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] butanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H40O7/c1-8-10-23(30)33-19-14-20-24(31-7)34-25(32-18(5)28)27(20)21(15-19)26(6,12-11-16(3)9-2)17(4)13-22(27)29/h9,11,14,17,19,21-22,24-25,29H,2,8,10,12-13,15H2,1,3-7H3/b16-11-/t17-,19+,21+,22+,24+,25-,26-,27-/m1/s1
InChI Key HYYVVSPRNZXNBO-MXRYFZCASA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H40O7
Molecular Weight 476.60 g/mol
Exact Mass 476.27740361 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.45
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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CHEMBL231215

2D Structure

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2D Structure of Caseargrewins G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 - 0.6330 63.30%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6315 63.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8409 84.09%
OATP1B3 inhibitior + 0.9164 91.64%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.7881 78.81%
P-glycoprotein inhibitior + 0.7316 73.16%
P-glycoprotein substrate + 0.5775 57.75%
CYP3A4 substrate + 0.6992 69.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8742 87.42%
CYP3A4 inhibition + 0.7985 79.85%
CYP2C9 inhibition - 0.7994 79.94%
CYP2C19 inhibition - 0.8143 81.43%
CYP2D6 inhibition - 0.9266 92.66%
CYP1A2 inhibition - 0.6774 67.74%
CYP2C8 inhibition + 0.6823 68.23%
CYP inhibitory promiscuity - 0.7999 79.99%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5638 56.38%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9351 93.51%
Skin irritation + 0.6453 64.53%
Skin corrosion - 0.9215 92.15%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7429 74.29%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8582 85.82%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.5794 57.94%
Acute Oral Toxicity (c) III 0.4653 46.53%
Estrogen receptor binding + 0.6894 68.94%
Androgen receptor binding + 0.5784 57.84%
Thyroid receptor binding - 0.5417 54.17%
Glucocorticoid receptor binding + 0.7620 76.20%
Aromatase binding + 0.7243 72.43%
PPAR gamma + 0.6927 69.27%
Honey bee toxicity - 0.7071 70.71%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9960 99.60%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.31% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.08% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.03% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.53% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.02% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.50% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.43% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.09% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.97% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.24% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 86.16% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.81% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.12% 92.94%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.91% 94.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.38% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.12% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.31% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 80.27% 94.73%

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.
Casearia grewiifolia

Cross-Links

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PubChem 16756886
LOTUS LTS0271551
wikiData Q105035545