Camptothecin, acetate

Details

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Internal ID 41598704-35e3-49af-a1e4-d3e6d59f45da
Taxonomy Alkaloids and derivatives > Camptothecins
IUPAC Name (19-ethyl-14,18-dioxo-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4,6,8,10,15(20)-heptaen-19-yl) acetate
SMILES (Canonical) CCC1(C2=C(COC1=O)C(=O)N3CC4=CC5=CC=CC=C5N=C4C3=C2)OC(=O)C
SMILES (Isomeric) CCC1(C2=C(COC1=O)C(=O)N3CC4=CC5=CC=CC=C5N=C4C3=C2)OC(=O)C
InChI InChI=1S/C22H18N2O5/c1-3-22(29-12(2)25)16-9-18-19-14(8-13-6-4-5-7-17(13)23-19)10-24(18)20(26)15(16)11-28-21(22)27/h4-9H,3,10-11H2,1-2H3
InChI Key ASVIEXKOXDCZDF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H18N2O5
Molecular Weight 390.40 g/mol
Exact Mass 390.12157168 g/mol
Topological Polar Surface Area (TPSA) 85.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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NSC95382
7688-64-4
NSC-95382
Neuro_000043
4-Ethyl-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl acetate
[ethyl(dioxo)[?]yl] acetate
CHEMBL2004368
SCHEMBL12045792
1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-(acetyloxy)-4-ethyl-, (S)-
NCI60_042119
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Camptothecin, acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9370 93.70%
Caco-2 - 0.7730 77.30%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.5317 53.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9237 92.37%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9448 94.48%
P-glycoprotein inhibitior + 0.6073 60.73%
P-glycoprotein substrate - 0.8319 83.19%
CYP3A4 substrate + 0.6508 65.08%
CYP2C9 substrate - 0.7913 79.13%
CYP2D6 substrate - 0.8928 89.28%
CYP3A4 inhibition + 0.8538 85.38%
CYP2C9 inhibition + 0.6014 60.14%
CYP2C19 inhibition + 0.6988 69.88%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition + 0.7342 73.42%
CYP2C8 inhibition + 0.4566 45.66%
CYP inhibitory promiscuity + 0.8824 88.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5324 53.24%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9636 96.36%
Skin irritation - 0.8410 84.10%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis + 0.5646 56.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6196 61.96%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.8806 88.06%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.8319 83.19%
Acute Oral Toxicity (c) III 0.4772 47.72%
Estrogen receptor binding + 0.9024 90.24%
Androgen receptor binding + 0.7629 76.29%
Thyroid receptor binding + 0.6798 67.98%
Glucocorticoid receptor binding + 0.7884 78.84%
Aromatase binding + 0.5329 53.29%
PPAR gamma + 0.7185 71.85%
Honey bee toxicity - 0.8913 89.13%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8821 88.21%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.08% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 98.03% 86.33%
CHEMBL2581 P07339 Cathepsin D 97.84% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.37% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 95.62% 97.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.72% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.46% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.32% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.56% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 83.16% 94.73%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.55% 93.40%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.30% 93.04%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.14% 96.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.82% 95.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.65% 100.00%

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.
Camptotheca acuminata

Cross-Links

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PubChem 98264
LOTUS LTS0209361
wikiData Q104918129