CID 73555

Details

Top
Internal ID b3485293-a7c4-4438-98bf-315375ceb640
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name (1R,3R,9S,24S,25S,32R)-20,24,32-trihydroxy-16-methoxy-29-methyl-6,10,18-trioxa-26,27-dithia-2,29-diazaheptacyclo[23.2.2.11,4.12,25.119,23.03,9.012,17]dotriaconta-4,7,12(17),13,15,19,21,23(31)-octaene-11,28,30-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H22N2O10S2/c1-28-24(34)27-22(32)14-11-37-9-8-16-19(14)29(27)25(35)26(28,40-41-27)21(31)12-6-7-15(30)18(10-12)38-20-13(23(33)39-16)4-3-5-17(20)36-2/h3-11,16,19,21-22,30-32H,1-2H3/t16-,19+,21-,22+,26-,27+/m0/s1
InChI Key VASYTSFNISZKEL-DCTKBWBHSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H22N2O10S2
Molecular Weight 598.60 g/mol
Exact Mass 598.07158725 g/mol
Topological Polar Surface Area (TPSA) 206.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 73555

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6970 69.70%
Caco-2 - 0.7998 79.98%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4645 46.45%
OATP2B1 inhibitior - 0.7142 71.42%
OATP1B1 inhibitior + 0.8657 86.57%
OATP1B3 inhibitior + 0.9310 93.10%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9476 94.76%
P-glycoprotein inhibitior + 0.7538 75.38%
P-glycoprotein substrate + 0.5723 57.23%
CYP3A4 substrate + 0.7146 71.46%
CYP2C9 substrate - 0.8050 80.50%
CYP2D6 substrate - 0.8297 82.97%
CYP3A4 inhibition - 0.7863 78.63%
CYP2C9 inhibition - 0.5663 56.63%
CYP2C19 inhibition - 0.5623 56.23%
CYP2D6 inhibition - 0.8035 80.35%
CYP1A2 inhibition - 0.6999 69.99%
CYP2C8 inhibition + 0.5998 59.98%
CYP inhibitory promiscuity - 0.6432 64.32%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5553 55.53%
Eye corrosion - 0.9826 98.26%
Eye irritation - 0.9238 92.38%
Skin irritation - 0.7653 76.53%
Skin corrosion - 0.9219 92.19%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5180 51.80%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.5179 51.79%
skin sensitisation - 0.8373 83.73%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5124 51.24%
Acute Oral Toxicity (c) III 0.5837 58.37%
Estrogen receptor binding + 0.7717 77.17%
Androgen receptor binding + 0.7666 76.66%
Thyroid receptor binding + 0.6863 68.63%
Glucocorticoid receptor binding + 0.7928 79.28%
Aromatase binding - 0.5228 52.28%
PPAR gamma + 0.7358 73.58%
Honey bee toxicity - 0.7106 71.06%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9874 98.74%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.62% 95.56%
CHEMBL2581 P07339 Cathepsin D 97.17% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.62% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.54% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.11% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.00% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.27% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.76% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.89% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.47% 93.40%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.87% 82.69%
CHEMBL1951 P21397 Monoamine oxidase A 88.35% 91.49%
CHEMBL2535 P11166 Glucose transporter 88.31% 98.75%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.17% 80.78%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.57% 100.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.66% 94.03%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 82.62% 96.86%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.62% 86.92%
CHEMBL3891 P07384 Calpain 1 80.21% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.11% 92.62%

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 73555
LOTUS LTS0125872
wikiData Q105282967