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PRD_001122

Summary
Name:CYCLOSPORIN D
Formula:C64 H115 N11 O12
Fomular weight:1230.664
Component type:peptide-like
Polymer sequences:DAL, MLE, MLE, MVA, BMT, VAL, MAA, MLE, VAL, MLE, ALA
Non-polymer components:
BIRD class:Immunosuppressant
Represented as:polymer
Compound Details:CYCLOSPORIN IS A CYCLIC UNDECAPEPTIDE. HERE, CYCLOSPORIN D IS REPRESENTED BY THE SEQUENCE (SEQRES)
Description:CYCLOSPORIN IS A CYCLIC UNDECAPEPTIDE. CYCLIZATION IS ACHIEVED BY LINKING THE N- AND THE C- TERMINI. CYCLOSPORIN D IS A NATURAL ANALOG OF CYCLOSPORIN A, OBTAINED FROM A DIFFERENT NUTRIENT BROTH AND DIFFERS FROM CYCLOSPORIN IN RESIDUE 6 (ABA6VAL). THE CYCLOSPORIN MOLECULE WAS MODIFIED AT POSITION 7 TO BE N-METHYL-L-ALANINE.
Families:FAM_000060

ProgramVersionName
ACDLabs12.01(3S,6S,9S,12R,15S,18S,21S,24S,27R,30S,33S)-33-[(1R,2R,4E)-1-hydroxy-2-methylhex-4-en-1-yl]-1,4,7,10,12,15,19,25,27,28-decamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21,30-tri(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
OpenEye OEToolkits1.7.6(3S,6S,9S,12R,15S,18S,21S,24S,27R,30S,33S)-1,4,7,10,12,15,19,25,27,28-decamethyl-33-[(E,1R,2R)-2-methyl-1-oxidanyl-hex-4-enyl]-6,9,18,24-tetrakis(2-methylpropyl)-3,21,30-tri(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

Chemical Descriptors

TypeProgramVersionDescriptor
SMILESACDLabs12.01O=C1N(C)C(C(=O)NC(C(=O)N(C(C(=O)N(C)C(C(=O)NC(C(=O)N(C)C(C(=O)NC(C(=O)NC(C(=O)N(C)C(C(=O)N(C)C(C(=O)N(C)C1C(C)C)CC(C)C)CC(C)C)C)C)CC(C)C)C(C)C)CC(C)C)C)C)C(C)C)C(O)C(C)C/C=C/C
InChIInChI1.03InChI=1S/C64H115N11O12/c1-27-28-29-41(16)53(76)52-57(80)68-49(38(10)11)62(85)69(20)44(19)59(82)70(21)46(31-35(4)5)56(79)67-50(39(12)13)63(86)71(22)45(30-34(2)3)55(78)65-42(17)54(77)66-43(18)58(81)72(23)47(32-36(6)7)60(83)73(24)48(33-37(8)9)61(84)74(25)51(40(14)15)64(87)75(52)26/h27-28,34-53,76H,29-33H2,1-26H3,(H,65,78)(H,66,77)(H,67,79)(H,68,80)/b28-27+/t41-,42+,43-,44-,45+,46+,47+,48+,49+,50+,51+,52+,53-/m1/s1
InChIKeyInChI1.03ZKBHJCJMHLTUOJ-RKWCNPPASA-N
SMILES_CANONICALCACTVS3.370C/C=C/C[C@@H](C)[C@@H](O)[C@@H]1N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)N(C)C(=O)[C@@H](NC1=O)C(C)C)C(C)C
SMILESCACTVS3.370CC=CC[CH](C)[CH](O)[CH]1N(C)C(=O)[CH](C(C)C)N(C)C(=O)[CH](CC(C)C)N(C)C(=O)[CH](CC(C)C)N(C)C(=O)[CH](C)NC(=O)[CH](C)NC(=O)[CH](CC(C)C)N(C)C(=O)[CH](NC(=O)[CH](CC(C)C)N(C)C(=O)[CH](C)N(C)C(=O)[CH](NC1=O)C(C)C)C(C)C
SMILES_CANONICALOpenEye OEToolkits1.7.6C/C=C/C[C@@H](C)[C@H]([C@H]1C(=O)N[C@H](C(=O)N([C@@H](C(=O)N([C@H](C(=O)N[C@H](C(=O)N([C@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N([C@H](C(=O)N([C@H](C(=O)N([C@H](C(=O)N1C)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)C)C)C(C)C)O
SMILESOpenEye OEToolkits1.7.6CC=CCC(C)C(C1C(=O)NC(C(=O)N(C(C(=O)N(C(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)N1C)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)C)C)C(C)C)O

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PDB entries from 2024-05-29

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