(1R,4R,5R,6R,8S,10R,12S,13S,16S,22R)-3',4,6,12,17,17-hexamethylspiro[9,18,23,24-tetraoxahexacyclo[20.2.1.01,13.04,12.05,10.016,22]pentacos-20-ene-8,5'-furan]-2',19-dione

Details

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Internal ID 964efc08-e3e5-498f-a147-58496ce58163
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (1R,4R,5R,6R,8S,10R,12S,13S,16S,22R)-3',4,6,12,17,17-hexamethylspiro[9,18,23,24-tetraoxahexacyclo[20.2.1.01,13.04,12.05,10.016,22]pentacos-20-ene-8,5'-furan]-2',19-dione
SMILES (Canonical) CC1CC2(C=C(C(=O)O2)C)OC3C1C4(CCC56CC7(C=CC(=O)OC(C7CCC5C4(C3)C)(C)C)OO6)C
SMILES (Isomeric) C[C@@H]1C[C@]2(C=C(C(=O)O2)C)O[C@H]3[C@H]1[C@]4(CC[C@@]56C[C@]7(C=CC(=O)OC([C@@H]7CC[C@H]5[C@@]4(C3)C)(C)C)OO6)C
InChI InChI=1S/C30H40O7/c1-17-13-30(14-18(2)24(32)35-30)33-19-15-27(6)21-8-7-20-25(3,4)34-22(31)9-10-28(20)16-29(21,37-36-28)12-11-26(27,5)23(17)19/h9-10,14,17,19-21,23H,7-8,11-13,15-16H2,1-6H3/t17-,19-,20+,21+,23+,26-,27+,28+,29-,30+/m1/s1
InChI Key DHOUAQSFGRJTAE-QVWAOBNKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H40O7
Molecular Weight 512.60 g/mol
Exact Mass 512.27740361 g/mol
Topological Polar Surface Area (TPSA) 80.30 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4R,5R,6R,8S,10R,12S,13S,16S,22R)-3',4,6,12,17,17-hexamethylspiro[9,18,23,24-tetraoxahexacyclo[20.2.1.01,13.04,12.05,10.016,22]pentacos-20-ene-8,5'-furan]-2',19-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 - 0.6720 67.20%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7090 70.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8838 88.38%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9680 96.80%
P-glycoprotein inhibitior + 0.7945 79.45%
P-glycoprotein substrate + 0.5327 53.27%
CYP3A4 substrate + 0.7047 70.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8728 87.28%
CYP3A4 inhibition - 0.7038 70.38%
CYP2C9 inhibition - 0.8660 86.60%
CYP2C19 inhibition - 0.8653 86.53%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.5349 53.49%
CYP2C8 inhibition + 0.7392 73.92%
CYP inhibitory promiscuity - 0.9232 92.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5587 55.87%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9158 91.58%
Skin irritation - 0.5674 56.74%
Skin corrosion - 0.8496 84.96%
Ames mutagenesis - 0.5870 58.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8398 83.98%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5654 56.54%
skin sensitisation - 0.7383 73.83%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6968 69.68%
Acute Oral Toxicity (c) III 0.4022 40.22%
Estrogen receptor binding + 0.8306 83.06%
Androgen receptor binding + 0.7581 75.81%
Thyroid receptor binding + 0.6401 64.01%
Glucocorticoid receptor binding + 0.7988 79.88%
Aromatase binding + 0.8308 83.08%
PPAR gamma + 0.6882 68.82%
Honey bee toxicity - 0.8143 81.43%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9949 99.49%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.35% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.92% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 91.15% 94.75%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.01% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.79% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.47% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.48% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.25% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.99% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.04% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.77% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.74% 97.14%
CHEMBL325 Q13547 Histone deacetylase 1 84.34% 95.92%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.32% 99.23%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.23% 96.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.16% 82.69%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.27% 96.77%

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.
Larix kaempferi

Cross-Links

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PubChem 101733485
LOTUS LTS0091402
wikiData Q104980642