Dihydromicromelin B

Details

Top
Internal ID f1a70353-557b-445e-95cc-025bc1e11499
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-[(1R,2R,4R,5R)-4-hydroxy-5-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]-7-methoxychromen-2-one
SMILES (Canonical) CC12C(O1)C(OC2O)C3=C(C=C4C(=C3)C=CC(=O)O4)OC
SMILES (Isomeric) C[C@]12[C@H](O1)[C@H](O[C@H]2O)C3=C(C=C4C(=C3)C=CC(=O)O4)OC
InChI InChI=1S/C15H14O6/c1-15-13(21-15)12(20-14(15)17)8-5-7-3-4-11(16)19-9(7)6-10(8)18-2/h3-6,12-14,17H,1-2H3/t12-,13-,14-,15-/m1/s1
InChI Key MBQNFMDTXFFAJQ-KBUPBQIOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H14O6
Molecular Weight 290.27 g/mol
Exact Mass 290.07903816 g/mol
Topological Polar Surface Area (TPSA) 77.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
94285-06-0
rel-6-[(1R,2R,4R,5R)-4-Hydroxy-5-methyl-3,6-dioxabicyclo[3.1.0]hex-2-yl]-7-methoxy-2H-1-benzopyran-2-one
AKOS032948293
FS-9184
6-((1R,2R,4R,5R)-4-Hydroxy-5-methyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl)-7-methoxy-2H-chromen-2-one
6-[(1R,2R,4R,5R)-4-HYDROXY-5-METHYL-3,6-DIOXABICYCLO[3.1.0]HEXAN-2-YL]-7-METHOXYCHROMEN-2-ONE

2D Structure

Top
2D Structure of Dihydromicromelin B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9765 97.65%
Caco-2 + 0.6812 68.12%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7706 77.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9074 90.74%
OATP1B3 inhibitior + 0.9101 91.01%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4939 49.39%
P-glycoprotein inhibitior - 0.7811 78.11%
P-glycoprotein substrate - 0.7401 74.01%
CYP3A4 substrate + 0.5838 58.38%
CYP2C9 substrate - 0.8234 82.34%
CYP2D6 substrate - 0.8556 85.56%
CYP3A4 inhibition + 0.8540 85.40%
CYP2C9 inhibition - 0.5465 54.65%
CYP2C19 inhibition + 0.6097 60.97%
CYP2D6 inhibition - 0.7509 75.09%
CYP1A2 inhibition - 0.9007 90.07%
CYP2C8 inhibition - 0.6280 62.80%
CYP inhibitory promiscuity - 0.5250 52.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4395 43.95%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9466 94.66%
Skin irritation - 0.7299 72.99%
Skin corrosion - 0.9560 95.60%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5803 58.03%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8441 84.41%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5295 52.95%
Acute Oral Toxicity (c) III 0.4720 47.20%
Estrogen receptor binding + 0.8190 81.90%
Androgen receptor binding + 0.6705 67.05%
Thyroid receptor binding - 0.6042 60.42%
Glucocorticoid receptor binding + 0.6665 66.65%
Aromatase binding + 0.6985 69.85%
PPAR gamma + 0.7202 72.02%
Honey bee toxicity - 0.8038 80.38%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5551 55.51%
Fish aquatic toxicity + 0.9399 93.99%

Targets

Top

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 97.81% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.49% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.11% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.39% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.34% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.68% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.48% 86.33%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.75% 94.03%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.61% 97.14%

Plants that contains it

Top
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.
Micromelum minutum

Cross-Links

Top
PubChem 91884873
LOTUS LTS0021586
wikiData Q105160912