Gex1Q1

Details

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Internal ID 7d1d01af-967b-487a-9041-c7762fb28a92
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name 2-[(2R,5S,6S)-4-hydroxy-6-[(2E,4E,6S)-7-[(2R,3R)-3-[(2R,3R,4R)-4-hydroxy-3-methoxypentan-2-yl]-2-methyloxiran-2-yl]-6-methylhepta-2,4-dien-2-yl]-5-methyloxan-2-yl]acetic acid
SMILES (Canonical) CC1C(CC(OC1C(=CC=CC(C)CC2(C(O2)C(C)C(C(C)O)OC)C)C)CC(=O)O)O
SMILES (Isomeric) C[C@@H]1[C@H](O[C@H](CC1O)CC(=O)O)/C(=C/C=C/[C@@H](C)C[C@@]2([C@H](O2)[C@H](C)[C@H]([C@@H](C)O)OC)C)/C
InChI InChI=1S/C25H42O7/c1-14(13-25(6)24(32-25)17(4)23(30-7)18(5)26)9-8-10-15(2)22-16(3)20(27)11-19(31-22)12-21(28)29/h8-10,14,16-20,22-24,26-27H,11-13H2,1-7H3,(H,28,29)/b9-8+,15-10+/t14-,16+,17-,18-,19-,20?,22-,23-,24-,25-/m1/s1
InChI Key HMVDRJCEIAATNJ-ZNLFPWLXSA-N
Popularity 38 references in papers

Physical and Chemical Properties

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Molecular Formula C25H42O7
Molecular Weight 454.60 g/mol
Exact Mass 454.29305367 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Gex1Q1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8641 86.41%
Caco-2 - 0.7152 71.52%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6020 60.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8300 83.00%
OATP1B3 inhibitior + 0.9275 92.75%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7106 71.06%
P-glycoprotein inhibitior - 0.5457 54.57%
P-glycoprotein substrate + 0.5085 50.85%
CYP3A4 substrate + 0.6570 65.70%
CYP2C9 substrate - 0.6176 61.76%
CYP2D6 substrate - 0.8734 87.34%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.8893 88.93%
CYP2C19 inhibition - 0.7989 79.89%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.8989 89.89%
CYP2C8 inhibition - 0.6196 61.96%
CYP inhibitory promiscuity - 0.9152 91.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8943 89.43%
Carcinogenicity (trinary) Non-required 0.5564 55.64%
Eye corrosion - 0.9834 98.34%
Eye irritation - 0.9609 96.09%
Skin irritation - 0.6146 61.46%
Skin corrosion - 0.9378 93.78%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6830 68.30%
Micronuclear - 0.5741 57.41%
Hepatotoxicity + 0.5757 57.57%
skin sensitisation - 0.7176 71.76%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7266 72.66%
Acute Oral Toxicity (c) III 0.5012 50.12%
Estrogen receptor binding + 0.5951 59.51%
Androgen receptor binding + 0.5601 56.01%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6449 64.49%
Aromatase binding - 0.4889 48.89%
PPAR gamma - 0.5083 50.83%
Honey bee toxicity - 0.6482 64.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.6511 65.11%

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 97.06% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.06% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.15% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 93.33% 91.19%
CHEMBL2581 P07339 Cathepsin D 92.88% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 92.26% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 87.93% 94.73%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 87.70% 98.75%
CHEMBL221 P23219 Cyclooxygenase-1 87.49% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.54% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.78% 96.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.51% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.59% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.89% 94.45%
CHEMBL2413 P32246 C-C chemokine receptor type 1 82.83% 89.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.94% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.50% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.96% 96.77%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.69% 97.14%
CHEMBL2996 Q05655 Protein kinase C delta 80.20% 97.79%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139585748
LOTUS LTS0106168
wikiData Q77490799