Citrofulvicin

Details

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Internal ID f0306b59-5bc5-49e9-8fe7-2f2835cd1890
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 7,8,19,20,27-pentahydroxy-1,25-dimethyl-11-oxo-4,16,24,28,29-pentaoxaoctacyclo[23.3.1.02,23.03,12.05,10.014,23.014,27.017,22]nonacosa-3(12),5(10),6,8,17(22),18,20-heptaene-9,21-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H22O15/c1-24-6-27(38)26-5-8-17(31)13-11(3-9(29)18(32)14(13)22(34)35)40-20(8)21(25(2,41-24)43-27)28(26,42-24)16-12(39-7-26)4-10(30)19(33)15(16)23(36)37/h3-4,21,29-30,32-33,38H,5-7H2,1-2H3,(H,34,35)(H,36,37)
InChI Key DVOCSTQKHJQOHL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H22O15
Molecular Weight 598.50 g/mol
Exact Mass 598.09586999 g/mol
Topological Polar Surface Area (TPSA) 239.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.53
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Citrofulvicin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7763 77.63%
Caco-2 - 0.8131 81.31%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6427 64.27%
OATP2B1 inhibitior - 0.5722 57.22%
OATP1B1 inhibitior + 0.8794 87.94%
OATP1B3 inhibitior + 0.9287 92.87%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6832 68.32%
P-glycoprotein inhibitior + 0.6250 62.50%
P-glycoprotein substrate + 0.6588 65.88%
CYP3A4 substrate + 0.6601 66.01%
CYP2C9 substrate + 0.6124 61.24%
CYP2D6 substrate - 0.8665 86.65%
CYP3A4 inhibition - 0.7941 79.41%
CYP2C9 inhibition - 0.9393 93.93%
CYP2C19 inhibition - 0.9383 93.83%
CYP2D6 inhibition - 0.9527 95.27%
CYP1A2 inhibition - 0.7498 74.98%
CYP2C8 inhibition + 0.7280 72.80%
CYP inhibitory promiscuity - 0.9856 98.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6308 63.08%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8615 86.15%
Skin irritation - 0.7798 77.98%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3647 36.47%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8481 84.81%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6374 63.74%
Acute Oral Toxicity (c) III 0.6211 62.11%
Estrogen receptor binding + 0.7749 77.49%
Androgen receptor binding + 0.7785 77.85%
Thyroid receptor binding + 0.5187 51.87%
Glucocorticoid receptor binding + 0.7657 76.57%
Aromatase binding + 0.7614 76.14%
PPAR gamma + 0.7004 70.04%
Honey bee toxicity - 0.8287 82.87%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9700 97.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.80% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.40% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.00% 89.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 93.40% 94.42%
CHEMBL2581 P07339 Cathepsin D 92.04% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.88% 99.23%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 91.48% 83.57%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.70% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.28% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.94% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.11% 96.09%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 84.28% 87.67%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.13% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.89% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.76% 85.14%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 81.23% 80.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.76% 89.34%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.63% 93.04%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.48% 85.11%

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.
There are no matching plants.

Cross-Links

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PubChem 139591156
LOTUS LTS0002849
wikiData Q103818735