Cephalostatin 5

Details

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Internal ID 54babf2c-1785-449b-8c82-c7f6354d5f5d
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Hydroxysteroids > 17-hydroxysteroids
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C54H72N2O10/c1-24-31-16-39(58)44-30-13-11-28-15-36-37(20-49(28,7)32(30)17-40(45(31)44)63-53(24)46(61)25(2)47(4,5)65-53)55-35-14-27-10-12-29-33(50(27,8)21-38(35)56-36)18-41(59)51(9)34(29)19-43-52(51,62)26(3)54(64-43)42(60)22-48(6,23-57)66-54/h17,19,24-29,31,33,39,41-43,46,57-62H,10-16,18,20-23H2,1-9H3
InChI Key RFXLQYCDXUKYKK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C54H72N2O10
Molecular Weight 909.20 g/mol
Exact Mass 908.51869650 g/mol
Topological Polar Surface Area (TPSA) 184.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.60
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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NSC 378731
121071-11-2

2D Structure

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2D Structure of Cephalostatin 5

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9771 97.71%
Caco-2 - 0.8589 85.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4462 44.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8317 83.17%
OATP1B3 inhibitior + 0.9177 91.77%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9751 97.51%
P-glycoprotein inhibitior + 0.7526 75.26%
P-glycoprotein substrate + 0.7291 72.91%
CYP3A4 substrate + 0.7422 74.22%
CYP2C9 substrate - 0.8114 81.14%
CYP2D6 substrate - 0.8001 80.01%
CYP3A4 inhibition - 0.8029 80.29%
CYP2C9 inhibition - 0.8324 83.24%
CYP2C19 inhibition - 0.8244 82.44%
CYP2D6 inhibition - 0.8796 87.96%
CYP1A2 inhibition - 0.5789 57.89%
CYP2C8 inhibition + 0.8327 83.27%
CYP inhibitory promiscuity - 0.5833 58.33%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5222 52.22%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9030 90.30%
Skin irritation - 0.7204 72.04%
Skin corrosion - 0.9299 92.99%
Ames mutagenesis + 0.5052 50.52%
Human Ether-a-go-go-Related Gene inhibition + 0.6713 67.13%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8422 84.22%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5977 59.77%
Acute Oral Toxicity (c) III 0.6410 64.10%
Estrogen receptor binding + 0.8023 80.23%
Androgen receptor binding + 0.7797 77.97%
Thyroid receptor binding + 0.5992 59.92%
Glucocorticoid receptor binding + 0.7455 74.55%
Aromatase binding + 0.6788 67.88%
PPAR gamma + 0.8135 81.35%
Honey bee toxicity - 0.6703 67.03%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9612 96.12%

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 98.92% 96.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 98.37% 89.05%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.77% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.78% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.50% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.64% 100.00%
CHEMBL1914 P06276 Butyrylcholinesterase 90.42% 95.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.26% 92.94%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 88.04% 100.00%
CHEMBL259 P32245 Melanocortin receptor 4 86.81% 95.38%
CHEMBL4208 P20618 Proteasome component C5 85.94% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.80% 95.89%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 85.50% 98.46%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.65% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.53% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.48% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 83.31% 95.93%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.11% 97.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.15% 99.17%

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 180011
LOTUS LTS0046646
wikiData Q105235698