Cephalostatin 16

Details

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Internal ID 0a27a33d-0257-4eda-b95c-d691fb4b0d4f
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H74N2O10/c1-27-32-13-14-33-34-12-10-30-18-38-40(22-48(30,7)51(34,61)24-42(58)50(32,33)26-64-54(27)43(59)23-45(3,4)66-54)56-37-17-29-9-11-31-35(47(29,6)21-39(37)55-38)19-41(57)49(8)36(31)20-44-53(49,62)28(2)52(65-44)16-15-46(5,60)25-63-52/h14,20,27-32,34-35,41,43-44,57,59-62H,9-13,15-19,21-26H2,1-8H3/t27-,28-,29+,30+,31-,32-,34+,35+,41-,43-,44+,46+,47+,48+,49-,50-,51-,52+,53-,54+/m1/s1
InChI Key BTYKYELOCDEYNL-SEUYVTEWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C54H74N2O10
Molecular Weight 911.20 g/mol
Exact Mass 910.53434656 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 5.65
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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CHEMBL2304376

2D Structure

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2D Structure of Cephalostatin 16

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9836 98.36%
Caco-2 - 0.8562 85.62%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4983 49.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8255 82.55%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9385 93.85%
P-glycoprotein inhibitior + 0.7533 75.33%
P-glycoprotein substrate + 0.7416 74.16%
CYP3A4 substrate + 0.7539 75.39%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8265 82.65%
CYP3A4 inhibition - 0.8953 89.53%
CYP2C9 inhibition - 0.8707 87.07%
CYP2C19 inhibition - 0.8655 86.55%
CYP2D6 inhibition - 0.9023 90.23%
CYP1A2 inhibition - 0.5880 58.80%
CYP2C8 inhibition + 0.8031 80.31%
CYP inhibitory promiscuity - 0.8356 83.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5058 50.58%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.9030 90.30%
Skin irritation - 0.7037 70.37%
Skin corrosion - 0.9305 93.05%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6593 65.93%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8309 83.09%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.9113 91.13%
Acute Oral Toxicity (c) III 0.6562 65.62%
Estrogen receptor binding + 0.7650 76.50%
Androgen receptor binding + 0.7777 77.77%
Thyroid receptor binding + 0.6096 60.96%
Glucocorticoid receptor binding + 0.7594 75.94%
Aromatase binding + 0.6437 64.37%
PPAR gamma + 0.7848 78.48%
Honey bee toxicity - 0.6569 65.69%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9480 94.80%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.76% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.02% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.52% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.04% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.62% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.12% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.00% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.95% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 91.55% 94.75%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 88.95% 96.39%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 87.91% 100.00%
CHEMBL4302 P08183 P-glycoprotein 1 87.51% 92.98%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 87.25% 97.33%
CHEMBL259 P32245 Melanocortin receptor 4 87.07% 95.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.35% 94.00%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 85.34% 98.46%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.21% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.16% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.45% 95.89%
CHEMBL1871 P10275 Androgen Receptor 81.53% 96.43%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.95% 97.14%
CHEMBL2581 P07339 Cathepsin D 80.82% 98.95%

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 71717873
LOTUS LTS0253847
wikiData Q104945962