Carmabin B

Details

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Internal ID 3a0459c6-bc8a-4069-9b86-30c171b27e39
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides
IUPAC Name N-[1-[[1-[[1-[[1-amino-3-(4-methoxyphenyl)-1-oxopropan-2-yl]-methylamino]-1-oxopropan-2-yl]-methylamino]-1-oxopropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]-N,2,4-trimethyl-9-oxodecanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H59N5O7/c1-26(15-13-14-16-28(3)46)23-27(2)38(49)45(8)35(25-31-17-11-10-12-18-31)37(48)42-29(4)39(50)43(6)30(5)40(51)44(7)34(36(41)47)24-32-19-21-33(52-9)22-20-32/h10-12,17-22,26-27,29-30,34-35H,13-16,23-25H2,1-9H3,(H2,41,47)(H,42,48)
InChI Key FZTCTTODSSJQQB-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C40H59N5O7
Molecular Weight 721.90 g/mol
Exact Mass 721.44144924 g/mol
Topological Polar Surface Area (TPSA) 159.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Carmabin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9657 96.57%
Caco-2 - 0.8390 83.90%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7043 70.43%
OATP2B1 inhibitior + 0.5773 57.73%
OATP1B1 inhibitior + 0.9016 90.16%
OATP1B3 inhibitior + 0.9298 92.98%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7572 75.72%
BSEP inhibitior + 0.9398 93.98%
P-glycoprotein inhibitior + 0.7976 79.76%
P-glycoprotein substrate + 0.8818 88.18%
CYP3A4 substrate + 0.6813 68.13%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.8089 80.89%
CYP3A4 inhibition + 0.7388 73.88%
CYP2C9 inhibition - 0.7612 76.12%
CYP2C19 inhibition - 0.6152 61.52%
CYP2D6 inhibition - 0.8411 84.11%
CYP1A2 inhibition - 0.9123 91.23%
CYP2C8 inhibition + 0.4751 47.51%
CYP inhibitory promiscuity - 0.7226 72.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.6208 62.08%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9191 91.91%
Skin irritation - 0.8269 82.69%
Skin corrosion - 0.9377 93.77%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7710 77.10%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.6059 60.59%
skin sensitisation - 0.9381 93.81%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8705 87.05%
Acute Oral Toxicity (c) III 0.7619 76.19%
Estrogen receptor binding + 0.8316 83.16%
Androgen receptor binding + 0.7742 77.42%
Thyroid receptor binding + 0.5865 58.65%
Glucocorticoid receptor binding + 0.7548 75.48%
Aromatase binding + 0.6380 63.80%
PPAR gamma + 0.7507 75.07%
Honey bee toxicity - 0.8017 80.17%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9588 95.88%

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 99.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.78% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.07% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 97.78% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.14% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.64% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 94.36% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.11% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 89.76% 94.73%
CHEMBL1255126 O15151 Protein Mdm4 89.08% 90.20%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.56% 95.89%
CHEMBL3837 P07711 Cathepsin L 87.02% 96.61%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.60% 93.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.40% 99.15%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.07% 100.00%
CHEMBL2535 P11166 Glucose transporter 83.77% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 81.88% 91.19%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.35% 90.24%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.80% 93.56%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.59% 92.29%

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 10771165
LOTUS LTS0034932
wikiData Q77479386