[(1S,2R,3R,4R,7R,8S,10Z,12S,13R,14R,15R,16R,17R)-2,15-diacetyloxy-8-chloro-3,14,16-trihydroxy-4,13-dimethyl-9-methylidene-5-oxospiro[6-oxatricyclo[11.4.0.03,7]heptadec-10-ene-17,2'-oxirane]-12-yl] acetate

Details

Top
Internal ID e2c12b65-d2ed-4120-8b06-06c2c5fcc9f2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name [(1S,2R,3R,4R,7R,8S,10Z,12S,13R,14R,15R,16R,17R)-2,15-diacetyloxy-8-chloro-3,14,16-trihydroxy-4,13-dimethyl-9-methylidene-5-oxospiro[6-oxatricyclo[11.4.0.03,7]heptadec-10-ene-17,2'-oxirane]-12-yl] acetate
SMILES (Canonical) CC1C(=O)OC2C1(C(C3C(C(C=CC(=C)C2Cl)OC(=O)C)(C(C(C(C34CO4)O)OC(=O)C)O)C)OC(=O)C)O
SMILES (Isomeric) C[C@H]1C(=O)O[C@@H]2[C@@]1([C@@H]([C@@H]3[C@@]([C@H](/C=C\C(=C)[C@@H]2Cl)OC(=O)C)([C@H]([C@H]([C@H]([C@]34CO4)O)OC(=O)C)O)C)OC(=O)C)O
InChI InChI=1S/C26H33ClO12/c1-10-7-8-15(36-12(3)28)24(6)18(25(9-35-25)20(32)17(19(24)31)37-13(4)29)22(38-14(5)30)26(34)11(2)23(33)39-21(26)16(10)27/h7-8,11,15-22,31-32,34H,1,9H2,2-6H3/b8-7-/t11-,15-,16-,17+,18+,19-,20+,21-,22+,24+,25-,26-/m0/s1
InChI Key HTDHEUULGXFIKK-RPZGWZLCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C26H33ClO12
Molecular Weight 573.00 g/mol
Exact Mass 572.1660542 g/mol
Topological Polar Surface Area (TPSA) 178.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.07
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(1S,2R,3R,4R,7R,8S,10Z,12S,13R,14R,15R,16R,17R)-2,15-diacetyloxy-8-chloro-3,14,16-trihydroxy-4,13-dimethyl-9-methylidene-5-oxospiro[6-oxatricyclo[11.4.0.03,7]heptadec-10-ene-17,2'-oxirane]-12-yl] acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9374 93.74%
Caco-2 - 0.7758 77.58%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6666 66.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8435 84.35%
OATP1B3 inhibitior + 0.9106 91.06%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7661 76.61%
P-glycoprotein inhibitior + 0.6789 67.89%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6915 69.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8818 88.18%
CYP3A4 inhibition - 0.8456 84.56%
CYP2C9 inhibition - 0.7594 75.94%
CYP2C19 inhibition - 0.7455 74.55%
CYP2D6 inhibition - 0.9003 90.03%
CYP1A2 inhibition - 0.7521 75.21%
CYP2C8 inhibition - 0.5628 56.28%
CYP inhibitory promiscuity - 0.6594 65.94%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9025 90.25%
Carcinogenicity (trinary) Danger 0.4478 44.78%
Eye corrosion - 0.9803 98.03%
Eye irritation - 0.9136 91.36%
Skin irritation - 0.6834 68.34%
Skin corrosion - 0.9077 90.77%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5153 51.53%
Micronuclear - 0.5541 55.41%
Hepatotoxicity + 0.5106 51.06%
skin sensitisation - 0.7673 76.73%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7286 72.86%
Acute Oral Toxicity (c) III 0.5094 50.94%
Estrogen receptor binding + 0.7579 75.79%
Androgen receptor binding + 0.6568 65.68%
Thyroid receptor binding + 0.6128 61.28%
Glucocorticoid receptor binding + 0.6761 67.61%
Aromatase binding + 0.6034 60.34%
PPAR gamma + 0.6609 66.09%
Honey bee toxicity - 0.5954 59.54%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9850 98.50%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.48% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.73% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.37% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 88.93% 91.19%
CHEMBL2581 P07339 Cathepsin D 88.14% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.13% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.99% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.08% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.30% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.79% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.36% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.23% 100.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.17% 94.42%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.62% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.12% 94.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 162880413
LOTUS LTS0241517
wikiData Q105033373