Homotectoridin

Details

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Internal ID fa23055e-a41b-4b32-b43b-5d6f68e35026
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavonoid O-glycosides
IUPAC Name 5-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-8-methoxy-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
SMILES (Canonical) COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=CC(=C3OC)OC4C(C(C(C(O4)CO)O)O)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=CC(=C3OC)O[C@H]4C([C@H]([C@@H](C(O4)CO)O)O)O)O)O
InChI InChI=1S/C23H24O12/c1-31-13-5-9(3-4-11(13)25)10-8-33-22-16(17(10)27)12(26)6-14(21(22)32-2)34-23-20(30)19(29)18(28)15(7-24)35-23/h3-6,8,15,18-20,23-26,28-30H,7H2,1-2H3/t15?,18-,19+,20?,23-/m1/s1
InChI Key LACQUZXTVNKQKI-QSXUWXSHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H24O12
Molecular Weight 492.40 g/mol
Exact Mass 492.12677620 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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Homotectorigenin 7-O-glucoside
5,7,4'-Trihydroxy-8,3'-dimethoxyisoflavone 7-O-glucoside
LMPK12050431

2D Structure

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2D Structure of Homotectoridin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5074 50.74%
Caco-2 - 0.8814 88.14%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6238 62.38%
OATP2B1 inhibitior - 0.6962 69.62%
OATP1B1 inhibitior + 0.9141 91.41%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6671 66.71%
P-glycoprotein inhibitior - 0.5810 58.10%
P-glycoprotein substrate - 0.8081 80.81%
CYP3A4 substrate + 0.6136 61.36%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.8862 88.62%
CYP2C9 inhibition - 0.9258 92.58%
CYP2C19 inhibition - 0.9329 93.29%
CYP2D6 inhibition - 0.9457 94.57%
CYP1A2 inhibition - 0.9089 90.89%
CYP2C8 inhibition + 0.6881 68.81%
CYP inhibitory promiscuity - 0.7195 71.95%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7238 72.38%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8750 87.50%
Skin irritation - 0.8305 83.05%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis - 0.5382 53.82%
Human Ether-a-go-go-Related Gene inhibition - 0.4594 45.94%
Micronuclear + 0.6733 67.33%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.9389 93.89%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7319 73.19%
Acute Oral Toxicity (c) III 0.6799 67.99%
Estrogen receptor binding + 0.8500 85.00%
Androgen receptor binding + 0.5501 55.01%
Thyroid receptor binding + 0.6086 60.86%
Glucocorticoid receptor binding + 0.7462 74.62%
Aromatase binding + 0.5617 56.17%
PPAR gamma + 0.7674 76.74%
Honey bee toxicity - 0.7907 79.07%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6149 61.49%
Fish aquatic toxicity + 0.7522 75.22%

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 99.02% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.47% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.00% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.24% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.35% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.78% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.94% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.78% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.28% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.76% 95.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.67% 96.21%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.14% 80.78%
CHEMBL4302 P08183 P-glycoprotein 1 84.61% 92.98%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.26% 96.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.78% 95.78%
CHEMBL3438 Q05513 Protein kinase C zeta 81.55% 88.48%
CHEMBL3194 P02766 Transthyretin 80.56% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 80.27% 94.73%

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.
Iris domestica
Iris tectorum

Cross-Links

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PubChem 44257366
NPASS NPC208972
LOTUS LTS0275678
wikiData Q104250899