Highly potent analogues of luteinizing hormone-releasing hormone containing D-phenylalanine nitrogen mustard in position 6. - Wikidata - wikimedia - TriplyDB

Highly potent analogues of luteinizing hormone-releasing hormone containing D-phenylalanine nitrogen mustard in position 6.

Highly potent analogues of luteinizing hormone-releasing hormone containing D-phenylalanine nitrogen mustard in position 6.

http://www.wikidata.org/entity/Q34297925

about

Cytotoxic analogs of luteinizing hormone-releasing hormone containing doxorubicin or 2-pyrrolinodoxorubicin, a derivative 500-1000 times more potent Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups Prostate cancer relevant antigens and enzymes for targeted drug delivery A chemically labeled cytotoxic agent: two-photon fluorophore for optical tracking of cellular pathway in chemotherapy Highly potent metallopeptide analogues of luteinizing hormone-releasing hormone.Receptor-targeting phthalocyanine photosensitizer for improving antitumor photocytotoxicity.Selective coupling of methotrexate to peptide hormone carriers through a gamma-carboxamide linkage of its glutamic acid moiety: benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate activation in salt coupling Short-chain analogs of luteinizing hormone-releasing hormone containing cytotoxic moieties.Inhibition of growth of experimental prostate cancer with sustained delivery systems (microcapsules and microgranules) of the luteinizing hormone-releasing hormone antagonist SB-75.Peptide-mediated targeted drug delivery.Luteinizing hormone-releasing hormone receptor targeted agents for prostate cancer.GnRH and GnRH receptors in the pathophysiology of the human female reproductive system.Comparative in vitro biological evaluation of daunorubicin containing GnRH-I and GnRH-II conjugates developed for tumor targeting.Gonadotropin-releasing hormone receptor-targeted paclitaxel-degarelix conjugate: synthesis and in vitro evaluation.Peptides and Drug Delivery.Synthesis and in vitro biochemical evaluation of oxime bond-linked daunorubicin-GnRH-III conjugates developed for targeted drug delivery.

P2860

Q24309593-41FA9021-722F-4CE3-BBE3-12A039870D9F Q24324532-1E5428AE-A19C-4DAE-A6BD-076FB0EB6C18 Q27013843-D5E908B8-B453-4BCD-9F9B-7CE9C1EFE926 Q30779111-16792E43-9F3E-46CE-BE15-EC1351F8C0F8 Q34297886-BA953960-65FE-4561-B1AE-9E0345A7E055 Q34302297-E1BB9926-8CA0-474B-ABE1-29636FE392F2 Q36409272-65449CA3-5EEE-4778-87E0-DE65BD2BECA7 Q37271561-FA7E33D8-9FCE-4804-B481-A46CDD230D60 Q37387473-0AE9F59A-CEF8-4491-BC81-4176EDA8F5A7 Q37785045-589DA818-1D08-4634-BE2B-4814CD155459 Q37859389-57542E54-C9E4-4409-B202-EA29E84EE214 Q38682630-DAD68552-6C3E-497A-AC4A-06413A03D8A5 Q38882916-78E9A3B6-30EE-45CF-B267-0E182CB21E2D Q42828662-9177AC0E-6439-4307-B23D-FC50A3E5F682 Q47590591-68E9F610-D1AA-4D9F-A3D7-5077C76D8309 Q55082165-2F820D70-DF3E-407E-B9C3-AD6500B243E3

P2860

Highly potent analogues of luteinizing hormone-releasing hormone containing D-phenylalanine nitrogen mustard in position 6.

http://www.wikidata.org/entity/Q34297925

description

1989 nî lūn-bûn

@nan

1989 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1989 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1989年の論文

@ja

1989年論文

@yue

1989年論文

@zh-hant

1989年論文

@zh-hk

1989年論文

@zh-mo

1989年論文

@zh-tw

1989年论文

@wuu

name

Highly potent analogues of lut ...... itrogen mustard in position 6.

@ast

Highly potent analogues of lut ...... itrogen mustard in position 6.

@en

Highly potent analogues of lut ...... itrogen mustard in position 6.

@nl

type

label

Highly potent analogues of lut ...... itrogen mustard in position 6.

@ast

Highly potent analogues of lut ...... itrogen mustard in position 6.

@en

Highly potent analogues of lut ...... itrogen mustard in position 6.

@nl

prefLabel

Highly potent analogues of lut ...... itrogen mustard in position 6.

@ast

Highly potent analogues of lut ...... itrogen mustard in position 6.

@en

Highly potent analogues of lut ...... itrogen mustard in position 6.

@nl

P1433

Q34297925-EB536D16-0B9A-4D55-919F-28FDF95CAC01

P1476

Q34297925-4057FD7B-3717-418E-8158-4C7D0EA0DAE0

P2093

Q34297925-60DE140C-0E3B-468D-8609-252E54B5BDD5

Q34297925-9E826AE2-2259-47E1-B9E9-7C4DC66739AE

Q34297925-B5FBA633-55AC-4297-8697-72835E2A9F19

Q34297925-BFA8A002-A20C-4EA4-9CA5-D9FBDDACF5DB

Q34297925-C79E9344-0ABC-4637-BB8B-89F5E4502622

Q34297925-E2B86ECB-4EE0-4FAF-BFD5-0C843CD1B063

Q34297925-E4EAA32F-7459-4E1E-BCFB-CAB4F8F672E0

Q34297925-F894DD22-AAB8-4163-9AB1-73A64D4DC050

P2860

Q34297925-2106E3FA-3D26-4DF6-A267-1AEB110C6775

Q34297925-2DAA419B-AAEA-466F-B5B0-9490DAB6BBF3

Q34297925-6CE252FA-B067-4CC9-BDA4-E00FA15CBC45

Q34297925-793563AB-1BF6-4347-BD8F-D44FA29F7892

Q34297925-7C9DBF37-1EB1-4AD8-B972-93DDB0F439ED

Q34297925-A266A5EA-B3E1-48F3-8FE7-0CC75007E5C7

Q34297925-AC2268EC-B7C8-402F-A1A7-78E360664B37

Q34297925-C116CEDB-CF31-42B4-8094-5E11CFA5D4AE

Q34297925-CFACA4F8-D9AA-4F11-9115-164E1E5639FF

Q34297925-DA273274-B7EB-4543-B3F2-F5527B0421E5

P304

Q34297925-894B5AAB-7B32-4938-A35F-554737B12DC8

P31

Q34297925-5E30D16A-71B7-4222-8AD8-4FBA69AFEC2C

P356

Q34297925-F1BECAC7-FCB2-4A51-AC45-20F6471770D1

P407

Q34297925-3CE7FD00-12B2-4A85-BE04-3E2F645779C7

P433

Q34297925-67D6AED2-779D-49EF-88D2-E5C9167EFD99

P478

Q34297925-63C52FF4-894B-4DAE-99F7-5A6930B64818

P577

Q34297925-797CF575-CAED-4341-94E0-1F6368F9BAF3

P5875

Q34297925-830A5C42-D210-456A-8ECF-06C9976FCD9C

P698

Q34297925-0000A644-BD26-4367-A46E-27EE7F03C394

P932

Q34297925-34D0703E-0BAF-4D81-BB86-9E95B2CA51CB

P356

PNAS.86.16.6318

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Highly potent analogues of lut ...... itrogen mustard in position 6.

@en

P2093

A V Schally

http://www.w3.org/2001/XMLSchema#string

G Srkalovic

http://www.w3.org/2001/XMLSchema#string

L Bokser

http://www.w3.org/2001/XMLSchema#string

M Fekete

http://www.w3.org/2001/XMLSchema#string

S Bajusz

http://www.w3.org/2001/XMLSchema#string

T Janaky

http://www.w3.org/2001/XMLSchema#string

T W Redding

http://www.w3.org/2001/XMLSchema#string

V J Csernus

http://www.w3.org/2001/XMLSchema#string

P2860

Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1-Hydroxy-benzotriazolen

Receptors for prolactin, somatostatin, and luteinizing hormone-releasing hormone in experimental prostate cancer after treatment with analogs of luteinizing hormone-releasing hormone and somatostatin.

Gonadotropin-releasing hormone analog design. Structure-function studies toward the development of agonists and antagonists: rationale and perspective.

New analogs of luliberin which inhibit ovulation in the rat.

Alkylating analogs of peptide hormones. 2. Synthesis and properties of p-(N,N-bis(2-chloroethyl)amino)phenylbutyryl derivatives of angiotensin II.

Comparison of different agonists and antagonists of luteinizing hormone-releasing hormone for receptor-binding ability to rat pituitary and human breast cancer membranes.

Alkylating analogs of peptide hormones. 1. Synthesis and properties of p-(N,N-)-bis(2-chloroethyl)amino)phenylbutyryl derivatives of bradykinin and bradykinin potentiating factor.

Analogues of luteinizing hormone releasing factor modified at positions 2, 6, and 10.

Interaction between hypothalamic peptides in a superfused pituitary cell system.

Gonadotropin-releasing hormone binding to rat anterior pituitary membrane homogenates. Comparison of antagonists and agonists using radiolabeled antagonist and agonist.

P304

6318-6322

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1073/PNAS.86.16.6318

http://www.w3.org/2001/XMLSchema#string

P407

P433

16

http://www.w3.org/2001/XMLSchema#string

P478

86

http://www.w3.org/2001/XMLSchema#string

P577

1989-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

20608360

http://www.w3.org/2001/XMLSchema#string

P698

2548207

http://www.w3.org/2001/XMLSchema#string

P932

297830

http://www.w3.org/2001/XMLSchema#string