Epothilone D1

Details

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Internal ID db85ce10-c448-42a6-9613-4294da3869f8
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (4S,7R,8S,9S,15Z,18S)-4,8-dihydroxy-5,7,9,11,15-pentamethyl-18-[(E)-1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-1-oxacyclooctadec-15-ene-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H45NO5S/c1-17-9-8-10-18(2)13-20(4)28(33)22(6)29(34)21(5)25(31)15-27(32)35-26(12-11-17)19(3)14-24-16-36-23(7)30-24/h11,14,16,18,20-22,25-26,28,31,33H,8-10,12-13,15H2,1-7H3/b17-11-,19-14+/t18?,20-,21?,22+,25-,26-,28-/m0/s1
InChI Key LUSOGNSOTZPASB-MHIRMNDESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H45NO5S
Molecular Weight 519.70 g/mol
Exact Mass 519.30184471 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.90
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Epothilone D1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9697 96.97%
Caco-2 - 0.7141 71.41%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Nucleus 0.7504 75.04%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.8535 85.35%
OATP1B3 inhibitior + 0.9236 92.36%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9524 95.24%
P-glycoprotein inhibitior + 0.6934 69.34%
P-glycoprotein substrate - 0.5247 52.47%
CYP3A4 substrate + 0.6656 66.56%
CYP2C9 substrate - 0.6127 61.27%
CYP2D6 substrate - 0.8780 87.80%
CYP3A4 inhibition - 0.7600 76.00%
CYP2C9 inhibition - 0.7808 78.08%
CYP2C19 inhibition - 0.6017 60.17%
CYP2D6 inhibition - 0.9052 90.52%
CYP1A2 inhibition + 0.5079 50.79%
CYP2C8 inhibition + 0.5550 55.50%
CYP inhibitory promiscuity - 0.9024 90.24%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5452 54.52%
Eye corrosion - 0.9845 98.45%
Eye irritation - 0.9523 95.23%
Skin irritation - 0.7055 70.55%
Skin corrosion - 0.9296 92.96%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7491 74.91%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6551 65.51%
skin sensitisation - 0.8306 83.06%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7659 76.59%
Nephrotoxicity - 0.6145 61.45%
Acute Oral Toxicity (c) III 0.5247 52.47%
Estrogen receptor binding + 0.6833 68.33%
Androgen receptor binding + 0.6432 64.32%
Thyroid receptor binding - 0.5537 55.37%
Glucocorticoid receptor binding + 0.6534 65.34%
Aromatase binding + 0.5250 52.50%
PPAR gamma + 0.5859 58.59%
Honey bee toxicity - 0.7682 76.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9760 97.60%

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
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.28% 99.23%
CHEMBL2581 P07339 Cathepsin D 94.17% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.33% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 87.65% 94.73%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.37% 87.67%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 85.21% 95.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.06% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.81% 85.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.32% 86.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.50% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.50% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.30% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.60% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.16% 95.50%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.82% 81.11%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 80.93% 98.46%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.82% 89.00%

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 23242269
LOTUS LTS0145618
wikiData Q75064121