Cytoglobosin B

Details

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Internal ID d6e585af-b726-474c-adc9-4d7db68d3e1f
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindolines > Isoindolones
IUPAC Name (1R,3E,5S,6R,7E,9S,11E,13R,14S,16S,17R,18S)-5,6,14-trihydroxy-18-(1H-indol-3-ylmethyl)-7,9,16-trimethyl-15-methylidene-19-azatricyclo[11.7.0.01,17]icosa-3,7,11-triene-2,20-dione
SMILES (Canonical) CC1CC=CC2C(C(=C)C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O
SMILES (Isomeric) C[C@H]\1C/C=C/[C@H]2[C@@H](C(=C)[C@H]([C@@H]3[C@@]2(C(=O)/C=C/[C@@H]([C@@H](/C(=C1)/C)O)O)C(=O)N[C@H]3CC4=CNC5=CC=CC=C54)C)O
InChI InChI=1S/C32H38N2O5/c1-17-8-7-10-23-30(38)20(4)19(3)28-25(15-21-16-33-24-11-6-5-9-22(21)24)34-31(39)32(23,28)27(36)13-12-26(35)29(37)18(2)14-17/h5-7,9-14,16-17,19,23,25-26,28-30,33,35,37-38H,4,8,15H2,1-3H3,(H,34,39)/b10-7+,13-12+,18-14+/t17-,19+,23-,25-,26-,28-,29+,30+,32+/m0/s1
InChI Key YUFTVRUFJJDEHE-ROQYSJLYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C32H38N2O5
Molecular Weight 530.70 g/mol
Exact Mass 530.27807232 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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CHEMBL1097578

2D Structure

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2D Structure of Cytoglobosin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9681 96.81%
Caco-2 - 0.8282 82.82%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5584 55.84%
OATP2B1 inhibitior - 0.7125 71.25%
OATP1B1 inhibitior + 0.8590 85.90%
OATP1B3 inhibitior + 0.9250 92.50%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9587 95.87%
P-glycoprotein inhibitior - 0.4600 46.00%
P-glycoprotein substrate + 0.6706 67.06%
CYP3A4 substrate + 0.7187 71.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.7597 75.97%
CYP2C9 inhibition - 0.6820 68.20%
CYP2C19 inhibition - 0.7228 72.28%
CYP2D6 inhibition - 0.8423 84.23%
CYP1A2 inhibition - 0.7938 79.38%
CYP2C8 inhibition + 0.6435 64.35%
CYP inhibitory promiscuity + 0.5563 55.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4406 44.06%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9529 95.29%
Skin irritation - 0.7682 76.82%
Skin corrosion - 0.9324 93.24%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4275 42.75%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5801 58.01%
skin sensitisation - 0.8458 84.58%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6101 61.01%
Acute Oral Toxicity (c) II 0.4297 42.97%
Estrogen receptor binding + 0.7017 70.17%
Androgen receptor binding + 0.6252 62.52%
Thyroid receptor binding + 0.6477 64.77%
Glucocorticoid receptor binding + 0.7527 75.27%
Aromatase binding + 0.5775 57.75%
PPAR gamma + 0.6896 68.96%
Honey bee toxicity - 0.6824 68.24%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9591 95.91%

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 99.00% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.43% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.91% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 95.11% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.72% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.38% 89.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 91.60% 88.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.23% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.36% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.83% 99.23%
CHEMBL213 P08588 Beta-1 adrenergic receptor 89.25% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.76% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.05% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 85.16% 97.79%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.91% 90.08%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 84.25% 97.64%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.70% 96.25%
CHEMBL4208 P20618 Proteasome component C5 83.24% 90.00%
CHEMBL255 P29275 Adenosine A2b receptor 82.65% 98.59%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.45% 96.39%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.47% 89.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.77% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.66% 86.33%
CHEMBL4530 P00488 Coagulation factor XIII 80.60% 96.00%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 80.03% 90.71%

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.
Eschweilera coriacea
Eucalyptus cladocalyx
Peltodon longipes
Salvadora persica

Cross-Links

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PubChem 46209793
NPASS NPC204491
LOTUS LTS0267668
wikiData Q105362811