LanguageCode

Attribute Information

Used By

Source

<xs:attribute name="LanguageCode" use="required">
  <xs:simpleType>
    <xs:restriction base="xs:token">
      <xs:enumeration value="cze"/>
      <xs:enumeration value="dut"/>
      <xs:enumeration value="eng"/>
      <xs:enumeration value="fin"/>
      <xs:enumeration value="fre"/>
      <xs:enumeration value="ger"/>
      <xs:enumeration value="ita"/>
      <xs:enumeration value="jpn"/>
      <xs:enumeration value="lav"/>
      <xs:enumeration value="por"/>
      <xs:enumeration value="scr"/>
      <xs:enumeration value="slv"/>
      <xs:enumeration value="spa"/>
    </xs:restriction>
  </xs:simpleType>
</xs:attribute>

Sample

C114158

quantum dye macrocyclic europium-chelate

1998

09

14

2003

08

08

a macrocyclic europium-chelate; structure in first source

2

*D005063

Europium

*D009942

Organometallic Compounds

Glycobiology 1998 Sep;8(9):849-56

M0294520

quantum dye macrocyclic europium-chelate

0

T324525

quantum dye macrocyclic europium-chelate

NLM (1998)

T324524

QD macrocyclic

NLM (1998)

C008718

osteoclast activating factor

1974

01

01

1982

07

28

found in supernatants of cultured human leukocytes; assayed by ability to stimulate bone resorption in organ culture in mechanism of localized bone loss

81

*D008222

Lymphokines

D001862

Bone Resorption

D010010

Osteoclasts

Ann N Y Acad Sci 230(0):474;1974

Ann N Y Acad Sci 256(0):133;1975

Calcif Tissue Int 1979;29(3):201

Calcif Tissue Res 1979;28(1):23

Cell Immunol 1980;49(1):74

Eur J Immunol 6:732;1976

J Clin Invest 64(1):337;1979

J Exp Med 149(1):279;1979

J Lab Clin Med 92(5):772;1978

Surg Clin North America 57(3):543;1977

WE 200 M486:127;1977

WE 200 M486:13;1977

WE 200 M486:319;1977

M0052808

osteoclast activating factor

64060-24-8

T082811

osteoclast activating factor

NLM (1974)

C008720

otoline

1974

01

01

1995

07

21

analog of cpd 48-80; oligomeric product (n-6-8); Russian drug

0

*D011108

Polymers

D006636

Histamine Release

Q000187

drug effects

Farmakol Toksikol 36(5):614;1973

M0052812

otoline

50643-04-4

T082815

otoline

NLM (1974)

C002540

miracil A

1972

01

01

2003

08

08

structure in first source

1

*ETHYLENEDIAMINES (72-75)

*XANTHENES (72-75)

D008154

Lucanthone

*Q000031

analogs & derivatives

Prog Drug Res 16:11;1972

M0043189

miracil A

9H-Xanthen-9-one, 1-((2-(diethylamino)ethyl)amino)-4-methyl-

3569-84-4

T073192

miracil A

NLM (1972)

C055240

Leakadine

1988

04

20

2001

02

06

may contain 2-carbamoylaziridine

8

*D001388

Aziridines

Vopr Onkol 1988;34(2):192

M0155620

Leakadine

91433-16-8

T185625

Leakadine

NLM (1988)

T185624

Leakadin

NLM (1988)

T185623

Leacadin

NLM (1988)

C060863

conduritol aziridine

1989

10

04

2005

11

03

inhibits both alpha- and beta-glucosidases; structure given in first source

2

*D001388

Aziridines

D007294

Inositol

*Q000031

analogs & derivatives

D050112

Imino Pyranoses

D001617

beta-Glucosidase

Q000037

antagonists & inhibitors

Biochem Biophys Res Commun 1989;163(1):495

M0168905

conduritol aziridine

7-Azabicyclo(4.1.0)heptane-2,3,4,5-tetrol, (1alpha,2alpha,3beta,4alpha,5beta,6alpha)-

123788-61-4

T198910

conduritol aziridine

NLM (1989)

T198909

1,2-dideoxy-1,2-iminoinositol

NLM (1989)

T198908

1,2-dideoxy-1,2-epimino-myo-inositol

NLM (1989)

C008725

1-oxacephalothin

1975

01

01

structure

0

D002512

Cephalothin

*Q000031

analogs & derivatives

J Am Chem Soc 96(24):7582;1974

M0052819

1-oxacephalothin

5-Oxa-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-((acetyloxy)methyl)-8-oxo-7-((2-thienylacetyl)amino)-, monosodium salt, trans-(+-)-

54214-84-5

T082822

1-oxacephalothin

NLM (1975)

C008727

oxaluric acid

1974

01

01

1990

09

28

11

*OXALATES (74-75)

AMIDES (74-75)

CARBAMATES (74-82)

D010072

Oxamic Acid

*Q000031

analogs & derivatives

J Bacteriol 117(3):1240;1974

M0052823

oxaluric acid

585-05-7

M0052823

M0052821

M0052823

M0052822

T082826

oxaluric acid

NLM (1974)

M0052821

carbamoyloxamic acid

M0052823

M0052821

T082824

carbamoyloxamic acid

NLM (1974)

M0052822

oxalurate

M0052823

M0052822

T082825

oxalurate

NLM (1974)

C414549

MB21 peptide

2000

10

24

2002

01

21

synthetic peptide with antimicrobial activity against a broad spectrum of microorganisms including various fungi; FYI - One other Medline citation (UI- 99402762 Appl Environ Microbiol 1999 Sep;65(9):4148-54) refers

3

*D010455

Peptides

Biochemistry 2000 Oct 3;39(39):11907-12

M0371423

MB21 peptide

0

T427025

MB21 peptide

2000

10

24

NLM (2000)

T427026

Ac-MB21-NH2

2000

10

24

NLM (2000)

T427027

FASLLGKALKALAKQ

2000

10

24

NLM (2000)

C008736

6-oxomestranol-6-(O-carboxymethyl)oxime

1974

01

01

1982

09

03

0

*NORPREGNANES (74-79)

*PREGNATRIENES (74-79)

KETOSTEROIDS (74-79)

OXIMES (74-82)

D008656

Mestranol

*Q000031

analogs & derivatives

Steroids 22(3):327;1973

M0052843

6-oxomestranol-6-(O-carboxymethyl)oxime

0

T082846

6-oxomestranol-6-(O-carboxymethyl)oxime

NLM (1974)

C008737

2-oxo-3-phenyl-1,2,3,4-tetrahydropyrido(2,3-c)pyrazine

1974

01

01

1982

09

07

structure

0

PYRIDINES (74-82)

*D011719

Pyrazines

J Med Chem 16(11):1296;1973

M0052844

2-oxo-3-phenyl-1,2,3,4-tetrahydropyrido(2,3-c)pyrazine

3,4-dihydro-3-phenylpyrido(3,4-b)pyrazin-2(1H)-one

43064-15-9

T082847

2-oxo-3-phenyl-1,2,3,4-tetrahydropyrido(2,3-c)pyrazine

NLM (1974)

C008738

9-oxoprostanoic acid

1974

01

01

1975

01

01

structure

0

*PROSTAGLANDINS (74-75)

CYCLOPENTANES (74-75)

FATTY ACIDS (74-75)

*D011466

Prostanoic Acids

Experientia 29(8):990;1973

M0052845

9-oxoprostanoic acid

64122-56-1

T082848

9-oxoprostanoic acid

NLM (1974)

C008739

7-oxo-delta(1)-tetrahydrocannabinol

1974

01

01

1975

01

01

aldehydic intermediate in metabolism of tetrahydrocannabinol; structure

0

*TETRAHYDROCANNABINOL (74-75)

ALDEHYDES (74-75)

D013759

Dronabinol

*Q000031

analogs & derivatives

Res Commun Chem Pathol Pharmacol 8(2):223;1974

M0052846

7-oxo-delta(1)-tetrahydrocannabinol

52663-85-1

T082849

7-oxo-delta(1)-tetrahydrocannabinol

NLM (1974)

C008722

methyl 6-(1,2,2-trichloroethenyl)imidazo(1,2-a)pyridine-2-carbamate

1982

01

26

2001

02

05

structure in first source

1

*D001562

Benzimidazoles

J Med Chem 1981;24(12):1518

M0052817

methyl 6-(1,2,2-trichloroethenyl)imidazo(1,2-a)pyridine-2-carbamate

Carbamic acid, (6-(trichloroethenyl)imidazo(1,2-a)pyridin-2-yl)-, methyl ester

71820-94-5

T082820

methyl 6-(1,2,2-trichloroethenyl)imidazo(1,2-a)pyridine-2-carbamate

NLM (1982)

T082819

MTCE-IPC

NLM (1982)

C008746

30-oxyethylated t-octyl phenol formaldehyde tetramer

1974

01

01

1997

08

13

reduces thromboatherosclerosis & cholesterol atherosclerosis; structure

0

*D011092

Polyethylene Glycols

D001161

Arteriosclerosis

Q000188

drug therapy

Exp Mol Pathol 20(2):154;1974

M0052859

30-oxyethylated t-octyl phenol formaldehyde tetramer

12584-89-3

T082862

30-oxyethylated t-octyl phenol formaldehyde tetramer

NLM (1974)

C009879

estane plastic

1975

01

01

2001

02

06

estane is urethane rubber

8

*D011140

Polyurethanes

Obstet Gynecol 45(3):287;1975

M0054951

estane plastic

0

M0054951

M0054950

T084954

estane plastic

NLM (1975)

M0054950

Estane 5714 F1

M0054951

M0054950

T084953

Estane 5714 F1

NLM (1975)

C008765

paracoccidioidin

1974

01

01

1993

02

10

35

*ANTIGENS, FUNGAL (74-79)

*COCCIDIOIDIN (74-92)

PARACOCCIDIOIDES (74-79)

*D005656

Fungal Proteins

Am J Trop Med Hyg 23(1):87;1974

Sabouraudia 16(2):93;1978

M0052899

paracoccidioidin

0

T082902

paracoccidioidin

NLM (1974)

C419503

plutonium hydroxide

2001

02

06

1

*D011005

Plutonium

Health Phys. 2001 Feb;80(2) :164-9

M0378031

plutonium hydroxide

0

T435350

plutonium hydroxide

2001

02

06

NLM (2001)

T435352

(239)Pu-hydroxide

2001

02

06

NLM (2001)

T435351

(239)plutonium hydroxide

2001

02

06

NLM (2001)

C084722

3,6-dimethyl-2,5-diaziridinylhydroquinone

1994

01

07

2001

02

06

hydroquinone form of the aziridinylbenzoquinone MeDZQ

1

*D001388

Aziridines

*D006873

Hydroquinones

Biochemistry 1993 Nov 30;32(47):12857-63

M0225024

3,6-dimethyl-2,5-diaziridinylhydroquinone

152923-07-4

T255029

3,6-dimethyl-2,5-diaziridinylhydroquinone

NLM (1994)

T255028

MeDZHQ

NLM (1994)

T255027

3,6-dimethyl-2,5-diaziridinyl-hydroquinone

NLM (1994)

C008784

pentafluorobenzylimine

1974

01

01

1982

09

14

0

IMINES (74-82)

*D005464

Fluorobenzenes

J Chromatogr Sci 12(7):411;1974

M0052947

pentafluorobenzylimine

0

T082950

pentafluorobenzylimine

NLM (1974)

C008786

3,5,5,O-3',5'-pentamethyl-2'-deoxydihydrouridine

1974

01

01

1990

08

22

structure

0

*DEOXYURIDINE (74-75)

METHYL ETHERS (74-75)

D003857

Deoxyuridine

*Q000031

analogs & derivatives

Biochim Biophys Acta 331(2):147;1973

M0052954

3,5,5,O-3',5'-pentamethyl-2'-deoxydihydrouridine

0

M0052954

M0052953

T082957

3,5,5,O-3',5'-pentamethyl-2'-deoxydihydrouridine

NLM (1974)

M0052953

2'-deoxy-3,5,5,O-3',5'-pentamethyldihydrouridine

M0052954

M0052953

T082956

2'-deoxy-3,5,5,O-3',5'-pentamethyldihydrouridine

NLM (1974)

C008796

S-pentyl-L-cysteine

1974

01

01

1975

01

01

structure

0

*CYSTEINE (74-75)

D003545

Cysteine

*Q000031

analogs & derivatives

Xenobiotica 3(4):207;1973

M0052966

S-pentyl-L-cysteine

4080-25-5

T082969

S-pentyl-L-cysteine

NLM (1974)

C008801

peptide PV

1974

01

01

0

*D010456

Peptides, Cyclic

J Gen Physiol 63(4):492;1974

M0052971

peptide PV

Cyclic(D-prolyl-D-valyl-L-prolyl-L-valyl-D-prolyl-D-valyl-L-prolyl-L-valyl-D-prolyl-D-valyl-L-prolyl-L-valyl)

38249-87-5

T082974

peptide PV

NLM (1974)

C008878

phosphatidylkojibiosyl diglyceride

1975

01

01

2001

02

05

structure

1

*PHOSPHOLIPIDS (75-76)

DIGLYCERIDES (75-76)

DISACCHARIDES (75-76)

*D006017

Glycolipids

*D010715

Phosphatidylglycerols

J Biol Chem 250(2):702;1975

M0053107

phosphatidylkojibiosyl diglyceride

0

T083110

phosphatidylkojibiosyl diglyceride

NLM (1975)

T083109

phosphatidylkojibiosyl diacylglycerol

NLM (1975)

C008826

phenacid

1972

01

01

2001

01

12

RN given refers to parent cpd; structure

17

PHENYLACETATES (72-82)

*D009588

Nitrogen Mustard Compounds

Biofizika 24(2):230;1979

Steroids 19(6):771;1972

M0053015

phenacid

10477-72-2

40068-28-8 (Na salt)

M0053015

M0310481

T083018

phenacid

NLM (1972)

T083017

phenylacetic mustard

NLM (1972)

T083016

p-(N,N-bis(2-chloroethyl)amino)phenylacetic acid

NLM (1972)

T083014

4-(N,N-bis(2-chloroethyl)amino)phenylacetic acid

NLM (1972)

T083015

chlorphenacyl

NLM (1972)

M0310481

phenacid, sodium salt

40068-28-8

M0053015

M0310481

T340481

phenacid, sodium salt

1999

08

18

NLM (1972)

C008814

peroben

1975

01

01

1982

08

02

hypnosedative combination of diphenhydramine & pyrithyldione

0

*D004155

Diphenhydramine

D004338

Drug Combinations

*D011728

Pyridones

Dermatologica 158(6):417;1979

Praxis 63(6):157;1974

M0052994

peroben

2,4(1H,3H)-Pyridinedione, 3,3-diethyl-, mixt. with 2-(diphenylmethoxy)-N,N-dimethylethanamine

78371-63-8

T082997

peroben

NLM (1975)

C008816

4-peroxycyclophosphamide

1974

01

01

1982

09

07

1

*CYCLOPHOSPHAMIDE (74-75)

PEROXIDES (74-82)

D003520

Cyclophosphamide

*Q000031

analogs & derivatives

J Am Chem Soc 96(12):4014;1974

M0052996

4-peroxycyclophosphamide

51274-71-6

T082999

4-peroxycyclophosphamide

NLM (1974)

C054080

lipid-associated sialic acid

1987

12

14

2001

04

05

elevated in patients with metastatic spread of laryngeal cancer; plasma levels of LASA-P may be correlated to alteration of cancer cells' surface membranes and thus may serve as a useful marker for malignant melanoma

67

*SIALIC ACIDS (87-96)

*D008055

Lipids

*D019158

N-Acetylneuraminic Acid

D014408

Biomarkers, Tumor

Clin Otolaryngol 1987;12(4):303

M0152917

lipid-associated sialic acid

0

T182922

lipid-associated sialic acid

NLM (1987)

T182921

LASA-P

NLM (1987)

T182920

LASA

NLM (1987)

C103995

plaunotol M-6

1997

02

21

2001

04

05

RN given for (E,Z,E)-isomer; structure in first source

2

*D005231

Fatty Acids, Unsaturated

J Antimicrob Chemother 1996 Sep;38(3):387-97

M0271766

plaunotol M-6

65811-39-4

65811-42-9 ((Z,E,E)-isomer)

M0271766

M0327738

T301771

plaunotol M-6

NLM (1997)

M0327738

plaunotol M-6, (Z,E,E)-isomer

65811-42-9

M0271766

M0327738

T357738

plaunotol M-6, (Z,E,E)-isomer

1999

08

18

NLM (1997)

C069989

serine containing aminolipid

1991

08

21

2001

04

05

analog of ornithine containing aminolipid; rarely present in bacteria; protects mice form lethal endotoxemia

6

*D008055

Lipids

D012694

Serine

*Q000031

analogs & derivatives

Infect Immun 1991;59(8):2560

M0190832

serine containing aminolipid

0

T220837

serine containing aminolipid

NLM (1991)

T220836

serine-containing lipid

NLM (1991)

T220835

Ser-L

NLM (1991)

C012409

lonetil M3

1976

01

01

2009

11

12

Russian Drug; structure

10

D008702

Methaqualone

*Q000031

analogs & derivatives

Act Nerv Super (Praha) 18(3):198;1976

Eksp Med Morfol 15(2):79;1976

M0059417

lonetil M3

1897-96-7

M0059417

M0059415

M0059417

M0059416

T089420

lonetil M3

NLM (1976)

M0059415

2-methyl-3(4-ethoxy)phenyl-4-quinazolone

M0059417

M0059415

T089418

2-methyl-3(4-ethoxy)phenyl-4-quinazolone

NLM (1976)

M0059416

lonetil

M0059417

M0059416

T089419

lonetil

NLM (1976)

C012411

lysometra

1976

01

01

1982

07

01

polypeptide preparation; low MW polypeptides obtained from hydrolysis of animal organs

0

*D010455

Peptides

Curr Med Res Opin 4(2):151;1976

M0059425

lysometra

0

T089428

lysometra

NLM (1976)

C012413

mastodynon

1976

01

01

1982

07

06

plant extract used therapeutically in breast diseases; mastodynon composition: 100 g Agnus castus D1, 20 g Caulophyllum thalictroides D4, 10 g Cyclamen D4, 10 g Ignatia D6, 10 g Iris D2, 20 g Lillum tigrinum D3, 10 g Lupulinum D8, 10 g Tinctura Condurango, 10 g Hersteller: Bionorica KG. 85 Nurnberg 1

13

*D010936

Plant Extracts

Fortschr Med 95(17):1175;1977

Med Welt 27(12):591;1976

ZFA (Stuttgart) 1979;55(22):1239

M0059426

mastodynon

Mastodynon

78200-25-6

T089429

mastodynon

NLM (1976)

C012421

3-methoxy-abeo-estrone

1976

01

01

1983

10

07

0

HOMOSTEROIDS (76-83)

D004970

Estrone

*Q000031

analogs & derivatives

Steroids 27(2):261;1976

M0059440

3-methoxy-abeo-estrone

3-methoxy-9(10-19)abeo-1,3,5(10)-estratrien- 17-one

0

T089443

3-methoxy-abeo-estrone

NLM (1976)

C012424

3 beta-methoxy-dinor-5-cholen-22-ol

1976

01

01

metabolite of cholesteryl methyl ether; structure

0

*D002770

Cholenes

Acta Microbiol 22(4):447;1975

M0059443

3 beta-methoxy-dinor-5-cholen-22-ol

0

T089446

3 beta-methoxy-dinor-5-cholen-22-ol

NLM (1976)

C012428

20-methylcholesterol

1976

01

01

0

D002784

Cholesterol

*Q000031

analogs & derivatives

J Org Chem 41(13):2288;1976

M0059449

20-methylcholesterol

Cholest-5-en-3-ol, 20-methyl-, (3beta)-

58958-29-5

T089452

20-methylcholesterol

NLM (1976)

C012431

2-O-methyl-D-glucuronic acid

1976

01

01

1982

07

12

0

METHYLGLYCOSIDES (76-82)

*D005965

Glucuronates

Biochem J 155(1):181;1976

M0059454

2-O-methyl-D-glucuronic acid

D-Glucuronic acid, 2-O-methyl-

59894-02-9

T089457

2-O-methyl-D-glucuronic acid

NLM (1976)

C012432

3-methyl-6-hydroxyquinazoline-2,4-dione

1976

01

01

0

*D011799

Quinazolines

C R Soc Biol (Paris) 169(5):1151;1975

M0059455

3-methyl-6-hydroxyquinazoline-2,4-dione

17730-75-5

T089458

3-methyl-6-hydroxyquinazoline-2,4-dione

NLM (1976)

C012433

1-methylinosine

1976

01

01

1979

11

29

20

D007288

Inosine

*Q000031

analogs & derivatives

Cancer 41(5):1685;1978

Clin Chim Acta 1979;97(2-3):159

J Am Chem Soc 98(9):2641;1976

Monogr Hum Genet 10:135;1978

M0059456

1-methylinosine

2140-73-0

T089459

1-methylinosine

NLM (1976)

C012441

N-methyl-alpha-tocopheramine nitroxide

1976

01

01

1995

03

30

structure

0

*VITAMIN E (83-95)

NITROGEN OXIDES (76-82)

D014810

Vitamin E

*Q000031

analogs & derivatives

Lipids 11(4):296;1976

M0059462

N-methyl-alpha-tocopheramine nitroxide

Nitroxide, 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl methyl

78249-60-2

T089465

N-methyl-alpha-tocopheramine nitroxide

NLM (1976)