Koranimine

Details

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Internal ID ad7c04e2-1e2b-47be-85f9-9331cd3765dc
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (3R,6S,9R,12R,15R,18S,21S)-3,9-dibenzyl-18-[(1R)-1-hydroxyethyl]-12,15-bis(2-methylpropyl)-6,21-di(propan-2-yl)-1,4,7,10,13,16,19-heptazacyclohenicos-19-ene-2,5,8,11,14,17-hexone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C44H65N7O7/c1-25(2)20-32-39(53)47-35(23-31-18-14-11-15-19-31)42(56)51-37(28(7)8)43(57)49-34(22-30-16-12-10-13-17-30)41(55)50-36(27(5)6)24-45-38(29(9)52)44(58)48-33(21-26(3)4)40(54)46-32/h10-19,24-29,32-38,52H,20-23H2,1-9H3,(H,46,54)(H,47,53)(H,48,58)(H,49,57)(H,50,55)(H,51,56)/t29-,32-,33-,34-,35-,36-,37+,38+/m1/s1
InChI Key HLSBKABOQXRVQW-ICZSIEETSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H65N7O7
Molecular Weight 804.00 g/mol
Exact Mass 803.49454744 g/mol
Topological Polar Surface Area (TPSA) 207.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 8
H-Bond Donor 7
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Koranimine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8762 87.62%
Caco-2 - 0.8584 85.84%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7088 70.88%
OATP2B1 inhibitior + 0.5690 56.90%
OATP1B1 inhibitior + 0.9080 90.80%
OATP1B3 inhibitior + 0.9245 92.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9399 93.99%
BSEP inhibitior + 0.9478 94.78%
P-glycoprotein inhibitior + 0.7553 75.53%
P-glycoprotein substrate + 0.5919 59.19%
CYP3A4 substrate + 0.5685 56.85%
CYP2C9 substrate - 0.6150 61.50%
CYP2D6 substrate - 0.8227 82.27%
CYP3A4 inhibition - 0.7674 76.74%
CYP2C9 inhibition - 0.8974 89.74%
CYP2C19 inhibition - 0.8219 82.19%
CYP2D6 inhibition - 0.9093 90.93%
CYP1A2 inhibition - 0.8680 86.80%
CYP2C8 inhibition - 0.6416 64.16%
CYP inhibitory promiscuity - 0.9423 94.23%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6922 69.22%
Carcinogenicity (trinary) Non-required 0.6546 65.46%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9157 91.57%
Skin irritation - 0.8076 80.76%
Skin corrosion - 0.9522 95.22%
Ames mutagenesis - 0.6554 65.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6560 65.60%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.5039 50.39%
skin sensitisation - 0.8712 87.12%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8484 84.84%
Acute Oral Toxicity (c) III 0.6391 63.91%
Estrogen receptor binding + 0.7573 75.73%
Androgen receptor binding + 0.6800 68.00%
Thyroid receptor binding + 0.5923 59.23%
Glucocorticoid receptor binding + 0.6884 68.84%
Aromatase binding + 0.5624 56.24%
PPAR gamma + 0.7494 74.94%
Honey bee toxicity - 0.9192 91.92%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5227 52.27%
Fish aquatic toxicity + 0.7457 74.57%

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
CHEMBL2581 P07339 Cathepsin D 99.28% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.09% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.38% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 92.74% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.60% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 92.48% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.38% 86.33%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 89.77% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.42% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.82% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.82% 95.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.67% 90.08%
CHEMBL1937 Q92769 Histone deacetylase 2 84.00% 94.75%
CHEMBL1949 P62937 Cyclophilin A 83.61% 98.57%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 53330673
LOTUS LTS0176042
wikiData Q75058436