33-(1-Hydroxy-2-methylhex-4-enyl)-1,4,7,12,15,19,25,28-octamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-30-propyl-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 f19a423c-5d65-4d49-8747-ebb58dc09840
Taxonomy Organic acids and derivatives > Peptidomimetics > Peptoid-peptide hybrids > Cyclosporins
IUPAC Name 33-(1-hydroxy-2-methylhex-4-enyl)-1,4,7,12,15,19,25,28-octamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-30-propyl-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) CCCC1C(=O)N(CC(=O)N(C(C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NC(C(=O)NC(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)CC(C)C)C)C(C)C)CC(C)C)C)C
SMILES (Isomeric) CCCC1C(=O)N(CC(=O)N(C(C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NC(C(=O)NC(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)CC(C)C)C)C(C)C)CC(C)C)C)C
InChI InChI=1S/C62H111N11O12/c1-24-26-28-40(15)52(75)51-57(80)65-43(27-25-2)58(81)68(18)33-48(74)69(19)45(30-35(5)6)56(79)67-49(38(11)12)61(84)70(20)46(31-36(7)8)55(78)64-41(16)53(76)63-42(17)54(77)66-44(29-34(3)4)59(82)71(21)47(32-37(9)10)60(83)72(22)50(39(13)14)62(85)73(51)23/h24,26,34-47,49-52,75H,25,27-33H2,1-23H3,(H,63,76)(H,64,78)(H,65,80)(H,66,77)(H,67,79)
InChI Key SPRAXCMVHXBDMZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C62H111N11O12
Molecular Weight 1202.60 g/mol
Exact Mass 1201.84136802 g/mol
Topological Polar Surface Area (TPSA) 288.00 Ų
XlogP 7.70
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 33-(1-Hydroxy-2-methylhex-4-enyl)-1,4,7,12,15,19,25,28-octamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-30-propyl-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 + 0.5454 54.54%
Caco-2 - 0.8587 85.87%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6572 65.72%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior - 0.5639 56.39%
OATP1B3 inhibitior - 0.4140 41.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9489 94.89%
P-glycoprotein inhibitior + 0.7432 74.32%
P-glycoprotein substrate + 0.8196 81.96%
CYP3A4 substrate + 0.7568 75.68%
CYP2C9 substrate - 0.8284 82.84%
CYP2D6 substrate - 0.8475 84.75%
CYP3A4 inhibition - 0.5117 51.17%
CYP2C9 inhibition - 0.9198 91.98%
CYP2C19 inhibition - 0.9047 90.47%
CYP2D6 inhibition - 0.9321 93.21%
CYP1A2 inhibition - 0.9147 91.47%
CYP2C8 inhibition + 0.6030 60.30%
CYP inhibitory promiscuity - 0.9967 99.67%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5990 59.90%
Eye corrosion - 0.9853 98.53%
Eye irritation - 0.8989 89.89%
Skin irritation - 0.7728 77.28%
Skin corrosion - 0.9009 90.09%
Ames mutagenesis - 0.5670 56.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4003 40.03%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.7807 78.07%
skin sensitisation - 0.8851 88.51%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6497 64.97%
Acute Oral Toxicity (c) III 0.7586 75.86%
Estrogen receptor binding + 0.7861 78.61%
Androgen receptor binding + 0.7255 72.55%
Thyroid receptor binding + 0.6475 64.75%
Glucocorticoid receptor binding + 0.7286 72.86%
Aromatase binding + 0.6226 62.26%
PPAR gamma + 0.8047 80.47%
Honey bee toxicity - 0.7621 76.21%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.6528 65.28%

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 99.51% 98.95%
CHEMBL1949 P62937 Cyclophilin A 99.41% 98.57%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.68% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.88% 96.09%
CHEMBL4072 P07858 Cathepsin B 92.77% 93.67%
CHEMBL321 P14780 Matrix metalloproteinase 9 92.09% 92.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.65% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 89.55% 94.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.06% 90.71%
CHEMBL5103 Q969S8 Histone deacetylase 10 87.73% 90.08%
CHEMBL299 P17252 Protein kinase C alpha 86.95% 98.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.85% 97.09%
CHEMBL333 P08253 Matrix metalloproteinase-2 86.42% 96.31%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.16% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.09% 89.00%
CHEMBL255 P29275 Adenosine A2b receptor 84.47% 98.59%
CHEMBL3392948 Q9NP59 Solute carrier family 40 member 1 84.36% 95.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.16% 99.23%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.46% 90.93%
CHEMBL2072 P35499 Sodium channel protein type IV alpha subunit 83.44% 92.32%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 83.36% 95.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.22% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.52% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.43% 93.56%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 82.00% 97.64%
CHEMBL332 P03956 Matrix metalloproteinase-1 81.30% 94.50%
CHEMBL4208 P20618 Proteasome component C5 80.81% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.79% 85.14%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.42% 82.38%

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 75015799
LOTUS LTS0123118
wikiData Q105257540