Microulin B

Details

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Internal ID 775bba18-3199-4b17-a9a4-b793d0e4e0e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [(1R,2R,4S,7S,8S,11R,12R,18R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosan-13-yl] 4-methoxybenzoate
SMILES (Canonical) CC1(C2CC(=O)C3(C(C2(C(CC(=O)O1)OC(=O)C4=CC=C(C=C4)OC)C)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C
SMILES (Isomeric) C[C@@]12CC[C@@H]3[C@@]4([C@@H](CC(=O)[C@]3([C@@]15[C@H](O5)C(=O)O[C@H]2C6=COC=C6)C)C(OC(=O)CC4OC(=O)C7=CC=C(C=C7)OC)(C)C)C
InChI InChI=1S/C34H38O10/c1-30(2)22-15-23(35)33(5)21(11-13-31(3)26(19-12-14-40-17-19)42-29(38)27-34(31,33)44-27)32(22,4)24(16-25(36)43-30)41-28(37)18-7-9-20(39-6)10-8-18/h7-10,12,14,17,21-22,24,26-27H,11,13,15-16H2,1-6H3/t21-,22+,24?,26+,27-,31+,32-,33+,34-/m1/s1
InChI Key LATWSCWLBNDHMY-RXVPQZJWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H38O10
Molecular Weight 606.70 g/mol
Exact Mass 606.24649740 g/mol
Topological Polar Surface Area (TPSA) 131.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.99
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Microulin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9777 97.77%
Caco-2 - 0.7792 77.92%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7324 73.24%
OATP2B1 inhibitior - 0.5693 56.93%
OATP1B1 inhibitior - 0.3660 36.60%
OATP1B3 inhibitior + 0.9713 97.13%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9831 98.31%
P-glycoprotein inhibitior + 0.8664 86.64%
P-glycoprotein substrate + 0.5290 52.90%
CYP3A4 substrate + 0.7165 71.65%
CYP2C9 substrate - 0.8114 81.14%
CYP2D6 substrate - 0.8406 84.06%
CYP3A4 inhibition + 0.8298 82.98%
CYP2C9 inhibition - 0.7972 79.72%
CYP2C19 inhibition - 0.7040 70.40%
CYP2D6 inhibition - 0.9077 90.77%
CYP1A2 inhibition - 0.7919 79.19%
CYP2C8 inhibition + 0.8405 84.05%
CYP inhibitory promiscuity - 0.8826 88.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5087 50.87%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8599 85.99%
Skin irritation - 0.7591 75.91%
Skin corrosion - 0.8891 88.91%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7488 74.88%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8455 84.55%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.5897 58.97%
Acute Oral Toxicity (c) III 0.3839 38.39%
Estrogen receptor binding + 0.8180 81.80%
Androgen receptor binding + 0.8138 81.38%
Thyroid receptor binding + 0.6567 65.67%
Glucocorticoid receptor binding + 0.8517 85.17%
Aromatase binding + 0.7415 74.15%
PPAR gamma + 0.7483 74.83%
Honey bee toxicity - 0.8189 81.89%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9882 98.82%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.64% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.60% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.78% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.69% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.92% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.70% 98.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.70% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.44% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.54% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.48% 92.62%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 87.18% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.64% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.61% 97.14%
CHEMBL4208 P20618 Proteasome component C5 86.53% 90.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.31% 100.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.72% 86.92%
CHEMBL221 P23219 Cyclooxygenase-1 84.11% 90.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.11% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 83.51% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.77% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 82.69% 87.67%
CHEMBL209 P07477 Trypsin I 82.43% 90.00%
CHEMBL3232685 O00257 E3 SUMO-protein ligase CBX4 81.49% 93.00%

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.
Microula sikkimensis
Morus alba

Cross-Links

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PubChem 101709115
NPASS NPC35249
LOTUS LTS0157878
wikiData Q105148936