Cryptophycin 16

Details

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Internal ID 6b68b7a3-c2f5-496c-aa22-fd061ba150f5
Taxonomy Organic acids and derivatives > Peptidomimetics > Hybrid peptides
IUPAC Name (3S,6R,10R,13E,16S)-10-[(3-chloro-4-hydroxyphenyl)methyl]-6-methyl-3-(2-methylpropyl)-16-[(1S)-1-[(2R,3R)-3-phenyloxiran-2-yl]ethyl]-1,4-dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone
SMILES (Canonical) CC1CNC(=O)C(NC(=O)C=CCC(OC(=O)C(OC1=O)CC(C)C)C(C)C2C(O2)C3=CC=CC=C3)CC4=CC(=C(C=C4)O)Cl
SMILES (Isomeric) C[C@@H]1CNC(=O)[C@H](NC(=O)/C=C/C[C@H](OC(=O)[C@@H](OC1=O)CC(C)C)[C@H](C)[C@@H]2[C@H](O2)C3=CC=CC=C3)CC4=CC(=C(C=C4)O)Cl
InChI InChI=1S/C34H41ClN2O8/c1-19(2)15-28-34(42)43-27(21(4)30-31(45-30)23-9-6-5-7-10-23)11-8-12-29(39)37-25(17-22-13-14-26(38)24(35)16-22)32(40)36-18-20(3)33(41)44-28/h5-10,12-14,16,19-21,25,27-28,30-31,38H,11,15,17-18H2,1-4H3,(H,36,40)(H,37,39)/b12-8+/t20-,21+,25-,27+,28+,30-,31-/m1/s1
InChI Key JPWBUGOVDPESSU-RNGXCZKDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H41ClN2O8
Molecular Weight 641.10 g/mol
Exact Mass 640.2551440 g/mol
Topological Polar Surface Area (TPSA) 144.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.43
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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DTXSID101046676
169181-93-5

2D Structure

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2D Structure of Cryptophycin 16

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9535 95.35%
Caco-2 - 0.8325 83.25%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6097 60.97%
OATP2B1 inhibitior + 0.5719 57.19%
OATP1B1 inhibitior + 0.8384 83.84%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9632 96.32%
P-glycoprotein inhibitior + 0.8887 88.87%
P-glycoprotein substrate + 0.7175 71.75%
CYP3A4 substrate + 0.6929 69.29%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.5859 58.59%
CYP2C9 inhibition - 0.8038 80.38%
CYP2C19 inhibition - 0.6796 67.96%
CYP2D6 inhibition - 0.8477 84.77%
CYP1A2 inhibition - 0.8273 82.73%
CYP2C8 inhibition + 0.7276 72.76%
CYP inhibitory promiscuity - 0.8515 85.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.4881 48.81%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9413 94.13%
Skin irritation - 0.7656 76.56%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.5937 59.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6820 68.20%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8414 84.14%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.5760 57.60%
Acute Oral Toxicity (c) III 0.5961 59.61%
Estrogen receptor binding + 0.8145 81.45%
Androgen receptor binding + 0.7716 77.16%
Thyroid receptor binding + 0.5776 57.76%
Glucocorticoid receptor binding + 0.7770 77.70%
Aromatase binding + 0.5524 55.24%
PPAR gamma + 0.8219 82.19%
Honey bee toxicity - 0.7860 78.60%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9844 98.44%

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 99.31% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.47% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 97.07% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.45% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 95.00% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.91% 96.09%
CHEMBL4208 P20618 Proteasome component C5 90.27% 90.00%
CHEMBL4040 P28482 MAP kinase ERK2 89.93% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.84% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.78% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.19% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.48% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.37% 93.99%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.76% 100.00%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 84.66% 92.29%
CHEMBL226 P30542 Adenosine A1 receptor 83.44% 95.93%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.54% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.40% 85.14%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.20% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.00% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.67% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.47% 89.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.52% 85.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.26% 97.25%

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.
Neurolaena lobata

Cross-Links

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PubChem 10604177
NPASS NPC219424
LOTUS LTS0003747
wikiData Q77492895