12,29-Bis(3-hydroxy-2-methylhex-4-en-2-yl)-7,13,17,24,30,34-hexaoxa-35,36-diazapentacyclo[30.2.1.115,18.06,8.023,25]hexatriaconta-1(35),2,4,9,15,18(36),19,21,26,32-decaene-14,31-dione

Details

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Internal ID 237fc4c3-f310-45be-ac59-6af038c0e26f
Taxonomy Organoheterocyclic compounds > Azoles > Oxazoles
IUPAC Name 12,29-bis(3-hydroxy-2-methylhex-4-en-2-yl)-7,13,17,24,30,34-hexaoxa-35,36-diazapentacyclo[30.2.1.115,18.06,8.023,25]hexatriaconta-1(35),2,4,9,15,18(36),19,21,26,32-decaene-14,31-dione
SMILES (Canonical) CC=CC(C(C)(C)C1CC=CC2C(O2)C=CC=CC3=NC(=CO3)C(=O)OC(CC=CC4C(O4)C=CC=CC5=NC(=CO5)C(=O)O1)C(C)(C)C(C=CC)O)O
SMILES (Isomeric) CC=CC(C(C)(C)C1CC=CC2C(O2)C=CC=CC3=NC(=CO3)C(=O)OC(CC=CC4C(O4)C=CC=CC5=NC(=CO5)C(=O)O1)C(C)(C)C(C=CC)O)O
InChI InChI=1S/C42H50N2O10/c1-7-15-33(45)41(3,4)35-21-13-19-31-29(51-31)17-9-12-24-38-44-28(26-50-38)40(48)54-36(42(5,6)34(46)16-8-2)22-14-20-32-30(52-32)18-10-11-23-37-43-27(25-49-37)39(47)53-35/h7-20,23-26,29-36,45-46H,21-22H2,1-6H3
InChI Key FOQGKCOTKQAXPE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C42H50N2O10
Molecular Weight 742.90 g/mol
Exact Mass 742.34654580 g/mol
Topological Polar Surface Area (TPSA) 170.00 Ų
XlogP 7.60
Atomic LogP (AlogP) 6.92
H-Bond Acceptor 12
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 12,29-Bis(3-hydroxy-2-methylhex-4-en-2-yl)-7,13,17,24,30,34-hexaoxa-35,36-diazapentacyclo[30.2.1.115,18.06,8.023,25]hexatriaconta-1(35),2,4,9,15,18(36),19,21,26,32-decaene-14,31-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8998 89.98%
Caco-2 - 0.8551 85.51%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5794 57.94%
OATP2B1 inhibitior + 0.7139 71.39%
OATP1B1 inhibitior + 0.8875 88.75%
OATP1B3 inhibitior + 0.9342 93.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9698 96.98%
P-glycoprotein inhibitior + 0.7979 79.79%
P-glycoprotein substrate - 0.6332 63.32%
CYP3A4 substrate + 0.6156 61.56%
CYP2C9 substrate - 0.8034 80.34%
CYP2D6 substrate - 0.8533 85.33%
CYP3A4 inhibition - 0.9397 93.97%
CYP2C9 inhibition - 0.8175 81.75%
CYP2C19 inhibition - 0.8491 84.91%
CYP2D6 inhibition - 0.9111 91.11%
CYP1A2 inhibition - 0.8336 83.36%
CYP2C8 inhibition - 0.6834 68.34%
CYP inhibitory promiscuity - 0.9473 94.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5315 53.15%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.9050 90.50%
Skin irritation - 0.7552 75.52%
Skin corrosion - 0.9188 91.88%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8384 83.84%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8226 82.26%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.7037 70.37%
Acute Oral Toxicity (c) III 0.4732 47.32%
Estrogen receptor binding + 0.8149 81.49%
Androgen receptor binding + 0.6414 64.14%
Thyroid receptor binding + 0.6648 66.48%
Glucocorticoid receptor binding + 0.7372 73.72%
Aromatase binding + 0.5729 57.29%
PPAR gamma + 0.7463 74.63%
Honey bee toxicity - 0.8572 85.72%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.7339 73.39%

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
CHEMBL2039 P27338 Monoamine oxidase B 93.03% 92.51%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.05% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.89% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 90.83% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 90.42% 89.63%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.24% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.22% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.25% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.00% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.71% 95.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.70% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.01% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.60% 93.65%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.70% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.75% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.52% 93.03%
CHEMBL4662 P28074 Proteasome Macropain subunit MB1 80.47% 93.85%

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.
Raputia praetermissa

Cross-Links

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PubChem 73698994
LOTUS LTS0099383
wikiData Q105161097