CID 101357919

Details

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Internal ID 6aeda858-39b5-41e1-a1a2-fa7dd33708c6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name
SMILES (Canonical) CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C
SMILES (Isomeric) C[C@@H]1C[C@H]([C@@H]2[C@@]([C@@]13CCC4(O3)CC(=O)OC4)(CCCC2(C)C)C)OC(=O)C
InChI InChI=1S/C22H34O5/c1-14-11-16(26-15(2)23)18-19(3,4)7-6-8-20(18,5)22(14)10-9-21(27-22)12-17(24)25-13-21/h14,16,18H,6-13H2,1-5H3/t14-,16-,18+,20+,21?,22-/m1/s1
InChI Key VMSPIYCFMMEMSY-QTHUDTEZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O5
Molecular Weight 378.50 g/mol
Exact Mass 378.24062418 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 101357919

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 + 0.6640 66.40%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8022 80.22%
OATP2B1 inhibitior - 0.8663 86.63%
OATP1B1 inhibitior + 0.8566 85.66%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.5662 56.62%
P-glycoprotein inhibitior + 0.6025 60.25%
P-glycoprotein substrate - 0.6720 67.20%
CYP3A4 substrate + 0.6717 67.17%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.8581 85.81%
CYP3A4 inhibition - 0.8955 89.55%
CYP2C9 inhibition - 0.7110 71.10%
CYP2C19 inhibition - 0.7546 75.46%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.9189 91.89%
CYP2C8 inhibition + 0.4938 49.38%
CYP inhibitory promiscuity - 0.9379 93.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5642 56.42%
Eye corrosion - 0.9785 97.85%
Eye irritation - 0.7814 78.14%
Skin irritation - 0.8023 80.23%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3761 37.61%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.6154 61.54%
skin sensitisation - 0.8771 87.71%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7701 77.01%
Acute Oral Toxicity (c) III 0.6411 64.11%
Estrogen receptor binding + 0.8372 83.72%
Androgen receptor binding + 0.6421 64.21%
Thyroid receptor binding + 0.7251 72.51%
Glucocorticoid receptor binding + 0.7553 75.53%
Aromatase binding + 0.7298 72.98%
PPAR gamma + 0.6689 66.89%
Honey bee toxicity - 0.7587 75.87%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9734 97.34%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.15% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.79% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.15% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.05% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.09% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.81% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.60% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.13% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.68% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 87.38% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.47% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.97% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.09% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.06% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.38% 82.69%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.36% 96.77%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.23% 93.04%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.79% 95.71%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.31% 94.08%
CHEMBL2996 Q05655 Protein kinase C delta 81.07% 97.79%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.30% 91.07%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.29% 92.94%

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.
Vitex trifolia
Vitex trifolia subsp. litoralis

Cross-Links

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PubChem 101357919
NPASS NPC121809
LOTUS LTS0165450
wikiData Q105289255