Desferrioxamine Te3

Details

Top
Internal ID f1e44c69-15bb-40b4-9563-502ab932b93f
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name 4,15,26-trihydroxy-1,12,23-trithia-4,9,15,20,26,31-hexazacyclotritriacontane-5,8,16,19,27,30-hexone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H42N6O9S3/c31-19-1-4-22(34)28(37)10-16-41-14-8-26-20(32)3-6-24(36)30(39)12-18-42-15-9-27-21(33)2-5-23(35)29(38)11-17-40-13-7-25-19/h37-39H,1-18H2,(H,25,31)(H,26,32)(H,27,33)
InChI Key UBAWUDQJFRYCRP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H42N6O9S3
Molecular Weight 654.80 g/mol
Exact Mass 654.21754046 g/mol
Topological Polar Surface Area (TPSA) 285.00 Ų
XlogP -3.50
Atomic LogP (AlogP) -0.46
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Desferrioxamine Te3

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5103 51.03%
Caco-2 - 0.8611 86.11%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.6930 69.30%
OATP2B1 inhibitior - 0.7144 71.44%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6663 66.63%
P-glycoprotein inhibitior + 0.5947 59.47%
P-glycoprotein substrate - 0.8617 86.17%
CYP3A4 substrate - 0.6087 60.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8401 84.01%
CYP3A4 inhibition - 0.8372 83.72%
CYP2C9 inhibition - 0.8500 85.00%
CYP2C19 inhibition - 0.8436 84.36%
CYP2D6 inhibition - 0.9013 90.13%
CYP1A2 inhibition - 0.8507 85.07%
CYP2C8 inhibition - 0.9879 98.79%
CYP inhibitory promiscuity - 0.9909 99.09%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.4708 47.08%
Eye corrosion - 0.9752 97.52%
Eye irritation - 0.8265 82.65%
Skin irritation - 0.7386 73.86%
Skin corrosion - 0.9189 91.89%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4857 48.57%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8611 86.11%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6423 64.23%
Acute Oral Toxicity (c) III 0.5637 56.37%
Estrogen receptor binding + 0.7080 70.80%
Androgen receptor binding - 0.5732 57.32%
Thyroid receptor binding + 0.5822 58.22%
Glucocorticoid receptor binding + 0.6612 66.12%
Aromatase binding + 0.6116 61.16%
PPAR gamma + 0.7125 71.25%
Honey bee toxicity - 0.9378 93.78%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.8664 86.64%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.39% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.20% 91.11%
CHEMBL2581 P07339 Cathepsin D 85.58% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.25% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.24% 99.23%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.14% 88.56%
CHEMBL255 P29275 Adenosine A2b receptor 80.59% 98.59%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.25% 93.10%

Plants that contains it

Top
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

Top
PubChem 14671628
LOTUS LTS0113588
wikiData Q77572652