30-Ethyl-33-(1-hydroxy-2-methylhex-4-enyl)-1,4,7,10,12,15,19,28-octamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone

Details

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Internal ID 8f65e383-3a4c-451f-ba89-48282d87b823
Taxonomy Organic acids and derivatives > Peptidomimetics > Peptoid-peptide hybrids > Cyclosporins
IUPAC Name 30-ethyl-33-(1-hydroxy-2-methylhex-4-enyl)-1,4,7,10,12,15,19,28-octamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
SMILES (Canonical) CCC1C(=O)N(CC(=O)NC(C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NC(C(=O)N(C(C(=O)N(C(C(=O)N(C(C(=O)N(C(C(=O)N1)C(C(C)CC=CC)O)C)C(C)C)C)CC(C)C)C)CC(C)C)C)C)C)CC(C)C)C)C(C)C)CC(C)C)C
SMILES (Isomeric) CCC1C(=O)N(CC(=O)NC(C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NC(C(=O)N(C(C(=O)N(C(C(=O)N(C(C(=O)N(C(C(=O)N1)C(C(C)CC=CC)O)C)C(C)C)C)CC(C)C)C)CC(C)C)C)C)C)CC(C)C)C)C(C)C)CC(C)C)C
InChI InChI=1S/C61H109N11O12/c1-24-26-27-39(15)51(74)50-55(78)65-42(25-2)57(80)67(18)32-47(73)64-43(28-33(3)4)53(76)66-48(37(11)12)60(83)68(19)44(29-34(5)6)54(77)62-40(16)52(75)63-41(17)56(79)69(20)45(30-35(7)8)58(81)70(21)46(31-36(9)10)59(82)71(22)49(38(13)14)61(84)72(50)23/h24,26,33-46,48-51,74H,25,27-32H2,1-23H3,(H,62,77)(H,63,75)(H,64,73)(H,65,78)(H,66,76)
InChI Key MIIRLHRXLLVIMF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C61H109N11O12
Molecular Weight 1188.60 g/mol
Exact Mass 1187.82571795 g/mol
Topological Polar Surface Area (TPSA) 288.00 Ų
XlogP 7.30
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 30-Ethyl-33-(1-hydroxy-2-methylhex-4-enyl)-1,4,7,10,12,15,19,28-octamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6464 64.64%
Caco-2 - 0.8580 85.80%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5714 57.14%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior - 0.6175 61.75%
OATP1B3 inhibitior - 0.5699 56.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9652 96.52%
P-glycoprotein inhibitior + 0.7428 74.28%
P-glycoprotein substrate + 0.8045 80.45%
CYP3A4 substrate + 0.7586 75.86%
CYP2C9 substrate - 0.8284 82.84%
CYP2D6 substrate - 0.8475 84.75%
CYP3A4 inhibition - 0.6112 61.12%
CYP2C9 inhibition - 0.9230 92.30%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9265 92.65%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition + 0.5948 59.48%
CYP inhibitory promiscuity - 0.9968 99.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5869 58.69%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.8991 89.91%
Skin irritation - 0.7606 76.06%
Skin corrosion - 0.9104 91.04%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3860 38.60%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.8771 87.71%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7871 78.71%
Acute Oral Toxicity (c) III 0.7726 77.26%
Estrogen receptor binding + 0.7817 78.17%
Androgen receptor binding + 0.7127 71.27%
Thyroid receptor binding + 0.6325 63.25%
Glucocorticoid receptor binding + 0.7238 72.38%
Aromatase binding + 0.6077 60.77%
PPAR gamma + 0.7995 79.95%
Honey bee toxicity - 0.7643 76.43%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.5926 59.26%

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
CHEMBL1949 P62937 Cyclophilin A 99.43% 98.57%
CHEMBL2581 P07339 Cathepsin D 99.28% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.27% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.58% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 94.94% 94.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 91.73% 90.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.55% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.73% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.03% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.25% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.10% 89.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.93% 96.61%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.71% 99.23%
CHEMBL321 P14780 Matrix metalloproteinase 9 84.24% 92.12%
CHEMBL2072 P35499 Sodium channel protein type IV alpha subunit 83.49% 92.32%
CHEMBL4208 P20618 Proteasome component C5 82.49% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.40% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 81.94% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.81% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.77% 100.00%
CHEMBL4072 P07858 Cathepsin B 81.33% 93.67%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.10% 93.56%
CHEMBL255 P29275 Adenosine A2b receptor 81.03% 98.59%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 80.95% 95.00%
CHEMBL333 P08253 Matrix metalloproteinase-2 80.47% 96.31%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.46% 90.93%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.38% 82.38%
CHEMBL3401 O75469 Pregnane X receptor 80.26% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 43104
LOTUS LTS0248902
wikiData Q105164851