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Details

Stereochemistry ABSOLUTE
Molecular Formula C67H115N21O23S
Molecular Weight 1614.822
Optical Activity UNSPECIFIED
Defined Stereocenters 15 / 15
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PREIMPLANTATION FACTOR

SMILES

CC[C@H](C)[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](NC(=O)[C@@H](N)CCSC)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O

InChI

InChIKey=GLXYOFXNKBTMQL-YKCHQESGSA-N
InChI=1S/C67H115N21O23S/c1-7-34(4)52(86-55(99)37(17-12-23-74-67(72)73)78-62(106)51(33(2)3)85-54(98)36(70)20-26-112-6)63(107)80-39(16-9-11-22-69)65(109)87-24-13-18-45(87)60(104)75-30-48(92)77-43(31-89)58(102)76-35(5)53(97)81-40(27-47(71)91)56(100)79-38(15-8-10-21-68)64(108)88-25-14-19-46(88)61(105)84-44(32-90)59(103)82-41(28-49(93)94)57(101)83-42(66(110)111)29-50(95)96/h33-46,51-52,89-90H,7-32,68-70H2,1-6H3,(H2,71,91)(H,75,104)(H,76,102)(H,77,92)(H,78,106)(H,79,100)(H,80,107)(H,81,97)(H,82,103)(H,83,101)(H,84,105)(H,85,98)(H,86,99)(H,93,94)(H,95,96)(H,110,111)(H4,72,73,74)/t34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,51-,52-/m0/s1

HIDE SMILES / InChI

Molecular Formula C67H115N21O23S
Molecular Weight 1614.822
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 15 / 15
E/Z Centers 5
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 12:05:43 UTC 2023
Edited
by admin
on Sat Dec 16 12:05:43 UTC 2023
Record UNII
3K6A6FJ98O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PREIMPLANTATION FACTOR
Common Name English
L-ASPARTIC ACID, L-METHIONYL-L-VALYL-L-ARGINYL-L-ISOLEUCYL-L-LYSYL-L-PROLYLGLYCYL-L-SERYL-L-ALANYL-L-ASPARAGINYL-L-LYSYL-L-PROLYL-L-SERYL-L-.ALPHA.-ASPARTYL-
Systematic Name English
SYNTHETIC PREIMPLANTATION FACTOR
Common Name English
L-METHIONYL-L-VALYL-L-ARGINYL-L-ISOLEUCYL-L-LYSYL-L-PROLYLGLYCYL-L-SERYL-L-ALANYL-L-ASPARAGINYL-L-LYSYL-L-PROLYL-L-SERYL-L-.ALPHA.-ASPARTYL-L-ASPARTIC ACID
Systematic Name English
PIF-1
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 613417
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
FDA ORPHAN DRUG 622517
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
FDA ORPHAN DRUG 664918
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
Code System Code Type Description
FDA UNII
3K6A6FJ98O
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
PRIMARY
PUBCHEM
134687212
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
PRIMARY
NCI_THESAURUS
C95890
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
PRIMARY
CAS
485818-40-4
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
PIF-1
Created by admin on Sat Dec 16 12:05:43 UTC 2023 , Edited by admin on Sat Dec 16 12:05:43 UTC 2023
PRIMARY Human (80119 ) Summary: PIF1 is a 5-prime-to-3-prime DNA helicase that negatively regulates telomerase (see TERT; MIM 187270), a reverse transcriptase that maintains telomere length (Zhang et al., 2006 (PubMed 16522649)
Related Record Type Details
ACTIVE MOIETY
SummaryThis gene encodes a DNA-dependent adenosine triphosphate (ATP)-metabolizing enzyme that functions as a 5' to 3' DNA helicase. The encoded protein can resolve G-quadruplex structures and RNA-DNA hybrids at the ends of chromosomes. It also prevents telomere elongation by inhibiting the actions of telomerase. Alternative splicing and the use of alternative start codons results in multiple isoforms that are differentially localized to either the mitochondria or the nucleus. (provided by RefSeq, Nov 2013)