CHEBI:72305 - teduglutide

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name teduglutide
ChEBI ID CHEBI:72305
Definition A 33-membered polypeptide consisting of His, Gly, Asp, Gly, Ser, Phe, Ser, Asp, Glu, Met, Asn, Thr, Ile, Leu, Asp, Asn, Leu, Ala, Ala, Arg, Asp, Phe, Ile, Asn, Trp, Leu, Ile, Gln, Thr, Lys, Ile, Thr and Asp residues joined in sequence. A glucagon-like peptide-2 receptor agonist used for the treatment of short-bowel syndrome.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C164H252N44O55S
Net Charge 0
Average Mass 3752.08200
Monoisotopic Mass 3749.79954
InChI InChI=1S/C164H252N44O55S/c1-21-77(11)126(156(255)187-95(44-46-114(167)214)141(240)206-130(83(17)211)160(259)186-93(42-33-34-49-165)140(239)202-129(80(14)24-4)159(258)208-131(84(18)212)161(260)200-111(163(262)263)66-125(230)231)203-151(250)100(54-76(9)10)189-145(244)103(57-88-67-175-92-41-32-31-40-90(88)92)192-147(246)105(60-116(169)216)199-157(256)127(78(12)22-2)204-152(251)102(56-87-38-29-26-30-39-87)190-149(248)109(64-123(226)227)195-137(236)94(43-35-50-174-164(171)172)183-134(233)82(16)179-133(232)81(15)180-142(241)98(52-74(5)6)188-146(245)104(59-115(168)215)194-150(249)110(65-124(228)229)196-143(242)99(53-75(7)8)198-158(257)128(79(13)23-3)205-162(261)132(85(19)213)207-153(252)106(61-117(170)217)193-139(238)97(48-51-264-20)185-138(237)96(45-47-120(220)221)184-148(247)108(63-122(224)225)197-155(254)113(72-210)201-144(243)101(55-86-36-27-25-28-37-86)191-154(253)112(71-209)182-119(219)70-177-136(235)107(62-121(222)223)181-118(218)69-176-135(234)91(166)58-89-68-173-73-178-89/h25-32,36-41,67-68,73-85,91,93-113,126-132,175,209-213H,21-24,33-35,42-66,69-72,165-166H2,1-20H3,(H2,167,214)(H2,168,215)(H2,169,216)(H2,170,217)(H,173,178)(H,176,234)(H,177,235)(H,179,232)(H,180,241)(H,181,218)(H,182,219)(H,183,233)(H,184,247)(H,185,237)(H,186,259)(H,187,255)(H,188,245)(H,189,244)(H,190,248)(H,191,253)(H,192,246)(H,193,238)(H,194,249)(H,195,236)(H,196,242)(H,197,254)(H,198,257)(H,199,256)(H,200,260)(H,201,243)(H,202,239)(H,203,250)(H,204,251)(H,205,261)(H,206,240)(H,207,252)(H,208,258)(H,220,221)(H,222,223)(H,224,225)(H,226,227)(H,228,229)(H,230,231)(H,262,263)(H4,171,172,174)/t77-,78-,79-,80-,81-,82-,83+,84+,85+,91-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,126-,127-,128-,129-,130-,131-,132-/m0/s1
InChIKey CILIXQOJUNDIDU-ASQIGDHWSA-N
SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(O)=O
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): glucagon-like peptide-2 receptor agonist
An agonist that binds to and activates glucagon-like peptide-2 (GLP-2) receptors.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): protective agent
Synthetic or natural substance which is given to prevent a disease or disorder or are used in the process of treating a disease or injury due to a poisonous agent.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing teduglutide (CHEBI:72305) has role antioxidant (CHEBI:22586)
teduglutide (CHEBI:72305) has role glucagon-like peptide-2 receptor agonist (CHEBI:72311)
teduglutide (CHEBI:72305) has role metabolite (CHEBI:25212)
teduglutide (CHEBI:72305) has role protective agent (CHEBI:50267)
teduglutide (CHEBI:72305) is a polypeptide (CHEBI:15841)
IUPAC Name
L-histidylglycyl-L-α-aspartylglycyl-L-seryl-L-phenylalanyl-L-seryl-L-α-aspartyl-L-α-glutamyl-L-methionyl-L-asparaginyl-L-threonyl-L-isoleucyl-L-leucyl-L-α-aspartyl-L-asparaginyl-L-leucyl-L-alanyl-L-alanyl-L-arginyl-L-α-aspartyl-L-phenylalanyl-L-isoleucyl-L-asparaginyl-L-tryptophyl-L-leucyl-L-isoleucyl-L-glutaminyl-L-threonyl-L-lysyl-L-isoleucyl-L-threonyl-L-aspartic acid
INN Source
teduglutide KEGG DRUG
Synonyms Sources
(Gly2)GLP-2 ChemIDplus
ALX 0600 ChemIDplus
ALX-0600 ChemIDplus
Glucagon-like peptide II (2-glycine) (human) ChemIDplus
Gly(2)-GLP-2 ChemIDplus
HGDGSFSDEMNTILDNLAARDFINWLIQTKITD ChEBI
His-Gly-Asp-Gly-Ser-Phe-Ser-Asp-Glu-Met-Asn-Thr-Ile-Leu-Asp-Asn-Leu-Ala-Ala-Arg-Asp-Phe-Ile-Asn-Trp-Leu-Ile-Gln-Thr-Lys-Ile-Thr-Asp ChEBI
Brand Name Source
Gattex ChemIDplus
Manual Xrefs Databases
4718 DrugCentral
D06053 KEGG DRUG
Teduglutide Wikipedia
US2006135424 Patent
US2011172152 Patent
WO2007065147 Patent
View more database links
Registry Numbers Types Sources
15460110 Reaxys Registry Number Reaxys
197922-42-2 CAS Registry Number ChemIDplus
197922-42-2 CAS Registry Number KEGG DRUG
Citations Waiting for Citations Types Sources
19773525 PubMed citation Europe PMC
19821509 PubMed citation Europe PMC
19847163 PubMed citation Europe PMC
21153865 PubMed citation Europe PMC
21154171 PubMed citation Europe PMC
21317170 PubMed citation Europe PMC
21825090 PubMed citation Europe PMC
22016579 PubMed citation Europe PMC
22017694 PubMed citation Europe PMC
22224470 PubMed citation Europe PMC
22570676 PubMed citation Europe PMC
22951144 PubMed citation Europe PMC
22982184 PubMed citation Europe PMC
23059393 PubMed citation Europe PMC
23089542 PubMed citation Europe PMC
23187965 PubMed citation Europe PMC
23189208 PubMed citation Europe PMC
23331163 PubMed citation Europe PMC
23333663 PubMed citation Europe PMC
23343999 PubMed citation Europe PMC
Last Modified
22 February 2017