Herbadysidolide

Details

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Internal ID 7a14c6ae-b024-4eee-a76a-961cd851ac2d
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (2R,3aS,7aR)-3,3,6-trimethylspiro[3a,4,5,7a-tetrahydro-1H-indene-2,3'-oxolane]-2'-one
SMILES (Canonical) CC1=CC2CC3(CCOC3=O)C(C2CC1)(C)C
SMILES (Isomeric) CC1=C[C@H]2C[C@@]3(CCOC3=O)C([C@H]2CC1)(C)C
InChI InChI=1S/C15H22O2/c1-10-4-5-12-11(8-10)9-15(14(12,2)3)6-7-17-13(15)16/h8,11-12H,4-7,9H2,1-3H3/t11-,12-,15+/m0/s1
InChI Key LWKYOCBKCDIMKI-SLEUVZQESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 2
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 Herbadysidolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.8434 84.34%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5282 52.82%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9198 91.98%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.5593 55.93%
P-glycoprotein inhibitior - 0.9425 94.25%
P-glycoprotein substrate - 0.9126 91.26%
CYP3A4 substrate + 0.5827 58.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8011 80.11%
CYP3A4 inhibition - 0.8891 88.91%
CYP2C9 inhibition - 0.8617 86.17%
CYP2C19 inhibition + 0.5203 52.03%
CYP2D6 inhibition - 0.9112 91.12%
CYP1A2 inhibition - 0.7021 70.21%
CYP2C8 inhibition - 0.8767 87.67%
CYP inhibitory promiscuity - 0.9127 91.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5543 55.43%
Eye corrosion - 0.9407 94.07%
Eye irritation - 0.5389 53.89%
Skin irritation - 0.6243 62.43%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6240 62.40%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5980 59.80%
skin sensitisation + 0.5148 51.48%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5466 54.66%
Acute Oral Toxicity (c) III 0.7446 74.46%
Estrogen receptor binding - 0.7069 70.69%
Androgen receptor binding + 0.6014 60.14%
Thyroid receptor binding - 0.7173 71.73%
Glucocorticoid receptor binding - 0.6491 64.91%
Aromatase binding - 0.7659 76.59%
PPAR gamma - 0.7659 76.59%
Honey bee toxicity - 0.8897 88.97%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9847 98.47%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.10% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.04% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.73% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.48% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.49% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.75% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.22% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.42% 96.77%
CHEMBL1871 P10275 Androgen Receptor 83.86% 96.43%
CHEMBL1937 Q92769 Histone deacetylase 2 82.32% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.32% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.09% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.96% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.48% 86.33%

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.
Achillea leptophylla
Aldama cordifolia
Cordiera macrophylla
Dioscorea futschauensis
Dorstenia barnimiana
Petrosedum forsterianum
Rubia yunnanensis
Uvaria mocoli
Verbascum georgicum
Zieria chevalieri

Cross-Links

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PubChem 23425006
NPASS NPC283741
LOTUS LTS0199199
wikiData Q105158375