Hildecarpin

Details

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Internal ID ed187f22-44cb-4719-9ba8-7ce683a35380
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name (1S,12S)-15-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene-1,16-diol
SMILES (Canonical) COC1=C(C=C2C(=C1)C3C(CO2)(C4=CC5=C(C=C4O3)OCO5)O)O
SMILES (Isomeric) COC1=C(C=C2C(=C1)[C@H]3[C@@](CO2)(C4=CC5=C(C=C4O3)OCO5)O)O
InChI InChI=1S/C17H14O7/c1-20-13-2-8-11(4-10(13)18)21-6-17(19)9-3-14-15(23-7-22-14)5-12(9)24-16(8)17/h2-5,16,18-19H,6-7H2,1H3/t16-,17+/m0/s1
InChI Key DQXBSJMCLQLJKV-DLBZAZTESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 86.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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99624-64-3
3,6a-Dihydroxy-2-methoxy-8,9-methylenedioxypterocarpan
(1S,12S)-15-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene-1,16-diol
CHEBI:5718
DTXSID00331947
LMPK12070129
Q27106866

2D Structure

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2D Structure of Hildecarpin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9436 94.36%
Caco-2 + 0.5559 55.59%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6549 65.49%
OATP2B1 inhibitior - 0.7283 72.83%
OATP1B1 inhibitior + 0.9060 90.60%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6720 67.20%
P-glycoprotein inhibitior - 0.6775 67.75%
P-glycoprotein substrate - 0.8106 81.06%
CYP3A4 substrate + 0.5690 56.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6699 66.99%
CYP3A4 inhibition - 0.5458 54.58%
CYP2C9 inhibition - 0.7224 72.24%
CYP2C19 inhibition + 0.5463 54.63%
CYP2D6 inhibition + 0.5112 51.12%
CYP1A2 inhibition - 0.7359 73.59%
CYP2C8 inhibition + 0.4507 45.07%
CYP inhibitory promiscuity - 0.5105 51.05%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Warning 0.4003 40.03%
Eye corrosion - 0.9901 99.01%
Eye irritation + 0.8031 80.31%
Skin irritation - 0.7955 79.55%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8613 86.13%
Micronuclear + 0.7959 79.59%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7697 76.97%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5647 56.47%
Acute Oral Toxicity (c) III 0.7217 72.17%
Estrogen receptor binding + 0.8275 82.75%
Androgen receptor binding + 0.5911 59.11%
Thyroid receptor binding + 0.8046 80.46%
Glucocorticoid receptor binding + 0.8133 81.33%
Aromatase binding + 0.6591 65.91%
PPAR gamma + 0.8929 89.29%
Honey bee toxicity - 0.8398 83.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5251 52.51%
Fish aquatic toxicity - 0.3869 38.69%

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 98.84% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.58% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.62% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.25% 92.62%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 90.24% 82.67%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.17% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.93% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.55% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.24% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.17% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.28% 92.94%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.21% 94.80%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.86% 89.62%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 83.16% 80.96%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.17% 95.89%
CHEMBL2535 P11166 Glucose transporter 81.69% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.17% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.16% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.66% 99.15%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.55% 93.40%

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.
Aconitum japonicum
Nelumbo nucifera
Taxus cuspidata
Tephrosia hildebrandtii

Cross-Links

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PubChem 442773
NPASS NPC61219
LOTUS LTS0178098
wikiData Q105345898