Kitamycin C

Details

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Internal ID afef6e6b-54ca-4abd-8cc2-fa1f2870ed55
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids and derivatives
IUPAC Name 3-formamido-2-hydroxy-N-[(2R,3S,6S,7R,8R)-7-hydroxy-2,6-dimethyl-4,9-dioxo-8-pentyl-1,5-dioxonan-3-yl]benzamide
SMILES (Canonical) CCCCCC1C(C(OC(=O)C(C(OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)O
SMILES (Isomeric) CCCCC[C@@H]1[C@H]([C@@H](OC(=O)[C@H]([C@H](OC1=O)C)NC(=O)C2=C(C(=CC=C2)NC=O)O)C)O
InChI InChI=1S/C22H30N2O8/c1-4-5-6-8-15-18(26)13(3)32-22(30)17(12(2)31-21(15)29)24-20(28)14-9-7-10-16(19(14)27)23-11-25/h7,9-13,15,17-18,26-27H,4-6,8H2,1-3H3,(H,23,25)(H,24,28)/t12-,13+,15-,17+,18+/m1/s1
InChI Key YRNJCJVWYIMZEE-ASZYTAPTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H30N2O8
Molecular Weight 450.50 g/mol
Exact Mass 450.20021592 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Kitamycin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6914 69.14%
Caco-2 - 0.8277 82.77%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5762 57.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.4872 48.72%
OATP1B3 inhibitior - 0.2168 21.68%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9572 95.72%
BSEP inhibitior - 0.5638 56.38%
P-glycoprotein inhibitior - 0.6120 61.20%
P-glycoprotein substrate + 0.7398 73.98%
CYP3A4 substrate + 0.5978 59.78%
CYP2C9 substrate + 0.6034 60.34%
CYP2D6 substrate - 0.8485 84.85%
CYP3A4 inhibition + 0.7687 76.87%
CYP2C9 inhibition - 0.7999 79.99%
CYP2C19 inhibition - 0.8152 81.52%
CYP2D6 inhibition - 0.9121 91.21%
CYP1A2 inhibition - 0.8373 83.73%
CYP2C8 inhibition + 0.5185 51.85%
CYP inhibitory promiscuity - 0.7891 78.91%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6811 68.11%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9708 97.08%
Skin irritation - 0.8061 80.61%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7712 77.12%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8497 84.97%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5866 58.66%
Acute Oral Toxicity (c) III 0.7104 71.04%
Estrogen receptor binding + 0.6663 66.63%
Androgen receptor binding + 0.6716 67.16%
Thyroid receptor binding - 0.5378 53.78%
Glucocorticoid receptor binding + 0.6917 69.17%
Aromatase binding - 0.5313 53.13%
PPAR gamma + 0.6067 60.67%
Honey bee toxicity - 0.9150 91.50%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6513 65.13%
Fish aquatic toxicity + 0.9800 98.00%

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
CHEMBL2581 P07339 Cathepsin D 98.36% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 95.51% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.28% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 93.80% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.68% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.09% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.47% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.82% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.02% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.99% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 88.82% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.02% 93.56%
CHEMBL1951 P21397 Monoamine oxidase A 85.93% 91.49%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.77% 87.67%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.24% 95.58%
CHEMBL2535 P11166 Glucose transporter 85.07% 98.75%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.66% 94.33%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 81.94% 85.83%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.36% 96.77%

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 139591632
LOTUS LTS0273878
wikiData Q105352908